Lactic acid is an important commodity chemical having a wide range of applications. Microbial production effectively competes with chemical synthesis methods because biochemical synthesis permits the generation of either one of the two enantiomers with high optical purity at high yield and titer, a result which is particularly beneficial for the production of poly(lactic acid) polymers having specific properties. The commercial viability of microbial lactic acid production relies on utilization of inexpensive carbon substrates derived from agricultural or waste resources. Therefore, optimal lactic acid formation requires an understanding and engineering of both the competing pathways involved in carbohydrate metabolism, as well as pathways leading to potential by-products which both affect product yield. Recent research leverages those biochemical pathways, while researchers also continue to seek strains with improved tolerance and ability to perform under desirable industrial conditions, for example, of pH and temperature.
Similar content being viewed by others
Lactic acid is a three carbon α-hydroxycarboxylic acid with a single chiral center, which therefore exists as one of two stereoisomers, D-lactic acid and L-lactic acid. A weak acid with a pKA of 3.86, lactic acid (lactate) has a wide range of applications in the food, cosmetic, agricultural and pharmaceutical industries (Hofvendahl and Hahn-Hägerdal 2000; Datta and Henry 2006; Okano et al. 2010). Lactate is also of interest for its potential chemical conversion into other high volume chemicals, such as hydrogenation to 1,2-propanediol or dehydration to acrylic acid (Datta and Henry 2006; Gao et al. 2011). Lactic acid is principally used as the starting material for poly(lactic acid) (PLA), a renewable and biodegradable polymer (Wehrenberg 1981; Kharas et al. 1994). PLA can be produced via the cyclic dimer lactide which allows for a controlled polymer molecular weight (Drumright et al. 2000). Several properties of PLA including crystallinity and thermal stability are moreover impacted by the relative fraction of the l- and d- isomers either in the polymer chain or in blends (Gruber et al. 1992, 1996; Lunt 1998; Blomqvist 2001; de Jong et al. 2001; Tsuji 2002; Tsuji and Fukui 2003). Lactic acid produced from petrochemicals, however, results in a racemic mixture, whereas microorganisms can generate exclusively either l-lactic acid or d-lactic acid, depending on which lactate dehydrogenase (LDH) enzyme is expressed to convert pyruvate to lactate as the final biochemical step. Thus, a great advantage of the biological route is the generation of optically pure lactate which directly affects the subsequent polymer composition (Wehrenberg 1981; Blomqvist 2001; Tsuji 2002).
As a commodity chemical, lactic acid must be biologically produced from cheap starting materials derived from agricultural sources such as the carbohydrate glucose. The ultimate yield of lactic acid (i.e., g product generated per g substrate consumed) is determined both by the biochemical pathways in upper metabolism which convert the carbohydrate into metabolic intermediates and by pathways in lower metabolism which potentially generate undesirable by-products. Thus, research can broadly be categorized as affecting upper metabolism or lower metabolism.
Upper metabolism involved in lactic acid formation
Lactic Acid Bacteria (LAB) are classified as either homofermentative or heterofermentative based on the metabolism of glucose. Although the terms are typically applied to LAB, many other organisms that generate lactic acid share features of the same pathways and can be considered homofermentative or heterofermentative. As the name implies, a homofermentative lactic acid process is one which potentially generates lactate alone. In this case, glucose is metabolized through the Embden–Meyerhof–Parnas (EMP) pathway (Fig. 1a, b). Key enzymes in the EMP pathway include glucose-6P isomerase (EC 126.96.36.199), 6-phosphofructokinase (EC. 188.8.131.52), and fructose-bisphosphate aldolase (EC 184.108.40.206). Conversion of glucose exclusively through the EMP pathway leads to a maximum theoretical yield of 2 mol lactate per mol glucose:
In contrast, a heterofermentative lactic acid process is one in which a significant fraction of the glucose is metabolized via the phosphoketolase (PK) pathway (Fig. 1a): from six-carbon gluconate-6P, the enzyme 6-phosphogluconate dehydrogenase (EC 220.127.116.11) cleaves of a CO2 to form ribulose-5P, and then phosphoketolase (EC 18.104.22.168) generates glyceraldehyde-P and acetate-P. Once metabolism has committed to acetate-P formation, this 2-carbon metabolite is not readily converted “back” to a 3-carbon compound, constraining this pathway to a maximum theoretical yield of 1 mol lactate per mol glucose. If the acetate-P formed is hydrolyzed to acetate by acetate kinase, then the stoichiometric conversion of glucose through the PK pathway becomes:
Equation 2 is incomplete since NAD(P)H must be oxidized to complete a redox balance. Depending on enzymes present, NAD(P) is regenerated as a result of the reduction of O2 or the reduction of other metabolites.
A third pathway found in upper metabolism that influences lactic acid formation is the pentose phosphate (PP) pathway (Fig. 1b). In this pathway, the 5-carbon ribulose-5P formed through 6-phosphogluconate dehydrogenase partitions between xylulose-5P and ribose-5P (two 5-carbon compounds), that are reversibly shuttled through sedoheptulose-7P and glyceraldehyde-3P (7-carbon + 3-carbon), and erythrose-4P and fructose-6P (4-carbon + 6-carbon) by the actions of the key enzymes transaldolase (EC 22.214.171.124) and transketolase (EC 126.96.36.199). The EMP pathway mediates the conversion of the fructose-6P generated by the PP pathway ultimately into glyceraldehyde-3P. If glucose is metabolized exclusively through the PP pathway to glyceraldehyde-3P and fructose-6P and the latter is converted to glyceraldehyde-3P via the EMP pathway, then the maximum theoretical lactate yield is 1.67 mol per mol glucose:
Equation 3 is also incomplete, however, since additional reduced compounds (such as H2O) must be generated to satisfy the redox balance.
Many microorganisms are able to metabolize pentoses such as d-xylose or l-arabinose, leading to lactate formation. Of course, these organisms must have an appropriate transport mechanism and enzymes to enter one of the major pathways described above. Because the PK pathway partitions 5-carbon compounds directly into glyceraldehyde-3P and acetate-P, the conversion of pentoses through this pathway results in a maximum yield of 1 mol lactate per mol pentose. Using xylose as an example pentose:
Equation 4 is written with the assumptions that the product of the PK pathway, acetate-P, is converted entirely to acetate, and that xylose transport into the cell is by facilitated diffusion (and does not consume ATP).
Alternatively, pentoses such as d-xylose or l-arabinose can be metabolized by the PP pathway. Because this pathway does not commit the cells to acetate-P formation, the maximum theoretical yield of lactate in this case is 1.67 mol/mol pentose:
Importantly, because Eq. 5 is redox balanced, the conversion of pentoses to lactate can proceed like a homofermentative process if the PP pathway is the exclusive metabolic pathway used for the conversion. However, the PK pathway generates 2 ATP/mol xylose consumed (Eq. 4) while the PP pathway generates 0.67 ATP/mol xylose consumed (Eq. 5).
Many microbial species have two or three of these pathways, and thus the resulting intermediate lactate yield is determined by which pathway predominates under the particular growth conditions. Based on Eqs. 1–5, the theoretical lactate yield from glucose resulting from the EMP, PP or PK pathways is 2, 1.67 or 1 mol, respectively. The lactate yield from xylose resulting from the PP or phosphoketolase pathway is 1.67 or 1 mol, respectively. Thus, the greatest lactate yield occurs for cells which metabolize glucose exclusively through the EMP pathway and which metabolize pentoses exclusively through the PP pathway.
Conversion of pentoses to lactic acid
Since different pathways in upper metabolism affect the stoichiometry of lactate generation, lactic acid yield can be improved merely by modifying an organism to favor a higher yielding pathway. For example, for the conversion of arabinose, the endogenous phosphoketolase gene in Lactobacillus plantarum was substituted with the transketolase gene from Lactococcus lactis, thereby shifting the PK pathway to the PP pathway (Okano et al. 2009a). With this improved pathway, 50 g arabinose l−1 was converted to 38.6 g lactic acid l−1 (yield = 1.54 mol/mol = 0.77 g/g) in 27 h. Although Lb. plantarum cannot utilize xylose, the same strategy of removing the PK pathway and introducing the PP pathway allowed a strain which also expressed two xylose-assimilation genes to generate 41.2 g lactic acid l−1 from 50 g xylose l−1 (yield = 1.65 mol/mol = 0.82 g/g) in 60 h (Okano et al. 2009b). In both these studies with Lb. plantarum, using an ldhL mutant led predominantly to the d-lactate isomer. Introducing the Lactobacillus pentosus xylose-assimilating operon xylAB into Lb. plantarum ldhL with additional knockouts in two phosphoketolase genes and a chromosomally integrated transketolase gene (tkt) allowed the strain to generate 74 g d-lactic acid l−1 from a mixture of 25 g xylose l−1 and 75 g glucose l−1 in 36 h without catabolite repression (Yoshida et al. 2011).
An organism which is able to use xylose, L. lactis IO-1 uses the PP pathway, at least partly, because the microbe naturally attains a yield greater than 1 mol lactate/mol glucose (Tanaka et al. 2002). Merely increasing the culture xylose concentration increases the lactate yield. Subsequent sequencing showed that Lc. lactis IO-1 contains transketolase but no transaldolase, and thus is thought to use 6-phosphofructokinase and fructose bisphosphate aldolase as alternate enzymes to complete the higher yielding PP pathway (Kato et al. 2012). Furthermore, the strain exclusively produces L-lactic acid, as genes coding d-lactate dehydrogenase (D-LDH) and lactate racemase are absent (Shimizu-Kadota et al. 2013). As an alternative to maintaining a high xylose concentration, the native PK pathway can be eliminated by deleting the phosphoketolase gene (ptk) in Lc. lactis IL1403 (Shinkawa et al. 2011). A consequence of this knockout was a reduced rate of lactate formation, necessitating an additional copy of the transketolase gene (tkt) to restore the rate, and suggesting that lactate formation in Lc. lactis is limited by the flux through the PP pathway.
Conversion of sucrose to lactic acid
An E. coli engineered to accumulate D-lactic acid from sucrose was constructed by a knockout in the sucrose repressor gene (cscR), leading to 85 g D-lactic acid l−1 in 84 h with a yield of 0.85 g/g (Wang et al. 2012). A strain engineered to accumulate l-lactic acid, also evolved for improved growth on sucrose, resulted in the generation of 97 g l-lactic acid l−1 with a yield of 0.9 g/g in a defined medium containing sucrose (Wang et al. 2013). This strain also converts sugarcane molasses and corn steep liquor to 75 g l-lactic acid l−1 with a yield of 0.85 g/g (Wang et al. 2013).
The filamentous fungus Rhizopus oryzae has long been studied for lactic acid production (Zhou et al. 1999), and the microbe generates L-lactic acid from glucose, sucrose and starch (Zhang et al. 2007). Lactic acid production occurs only during growing conditions (Maas et al. 2008).
Conversion of lignocellulosic hydrolysates to lactic acid
Many agricultural substrates are composed of complex carbohydrates which must be hydrolyzed into their constituent sugars (“saccharification”) prior to being converted into any biochemical product such as lactic acid (“fermentation”). There are several strategies to carry out this overall process. The conventional process for starch materials involves a saccharification step with high temperature gelatinization, followed by a second, separate fermentation step by appropriate organisms. Similarly, lignocellulosic materials may be chemically hydrolyzed, for example with dilute acid, prior to their fermentation.
A significant amount of research over many years has focused on hydrolyzing various lignocellulosic materials chemically, followed by the fermentation of the resulting hydrolysate into useful products, and one product studied has been lactic acid. For example, corncobs hydrolyzed with dilute sulfuric acid yielded a hydrolysate of 26.5 g xylose l−1, 2.4 g glucose l−1, 3.2 g arabinose l−1 and 3.5 g acetic acid l−1 which, after vacuum evaporation, was converted to 80 g lactic acid l−1 with a yield of about 80 % based on total sugar using a R. oryzae adapted to the hydrolysate (Bai et al. 2008). Similarly, Bacillus generated 55 g l-lactic acid l−1 from acid-hydrolyzed sugar cane bagasse supplemented with salts and corn steep liquor (Patel et al. 2004).
In most lignocellulosic materials, the hemicellulose fraction is readily hydrolyzed, for example with hot water. Such hydrolysates contain predominantly xylose, but often significant fractions of other sugars, and this mixture is an attractive source of carbohydrates for lactic acid. The moderately thermophilic Bacillus coagulans MXL-9 (described in detail below), has been used to ferment a several hot water hydrolysates. For example, larch extracts composed of 45.8 g total sugars l−1 was converted to 40.5 g lactic acid l−1 after 50 h (Walton et al. 2010). These cells consumed the glucose and mannose first, after which the remaining sugars were metabolized.
Guo et al. (2010a) isolated LAB strains whichthat metabolized both hexoses and pentoses found in lignocellulosic hydrolysate. Using a corncob hydrolysate, Lactobacillus brevis S3F4 generated 39 g lactic acid l−1 from a mixture containing about 57 g mixed sugars l−1. Importantly, the Lb. brevis metabolized glucose and xylose simultaneously and showed no growth inhibition or reduced product formation in the presence of 10 mM furfural and ferulic acid. Guo et al. (2010b) solated over 100 strains of R. oryzae and examined them for lactic acid production. One strain (GY18) converted the sugar mixture found in corncorb hydrolysate (233 g xylose and 39 g glucose per kg corncob) to lactic acid, although the microbe consumed xylose only after glucose was exhausted.
Simultaneous saccharification and fermentation for lactic acid formation
Another approach to sequential saccharification then fermentation involves “simultaneous saccharification and fermentation” (SSF), which increases volumetric productivity by combining otherwise sequential processes. This strategy can be accomplished in several ways: (1) saccharifying enzymes and a fermenting microbe are added simultaneously to the substrates, (2) a saccharifying microbe and a fermenting microbe are added simultaneously to the substrates, and (3) a single microbe is used which is able itself to saccharify the substrate and ferment the intermediate sugars.
Lactic acid may also be produced using SSF. This topic has been reviewed (John et al. 2009), and it continues to be a fruitful area of research. For example, using 275 g starch-containing cassava powder l−1 with 20 U glucoamylase l−1, Lactobacillus rhamnosus generated 175 g l-lactate l−1 in 96 h (Wang et al. 2010a). Similarly, Lactobacillus lactis converted 100 g cellobiose l−1 into about 80 g lactic acid l−1 in 48 h (Singhvi et al. 2010). Addition of cellulase into an SSF resulted in 73 g lactic acid l−1 from 100 g sugarcane bagasse-derived cellulose l−1 after 48 h (Singhvi et al. 2010). Similarly, a Lactobacillus delbrueckii which could utilize cellobiose converted 100 g pure cellobiose l−1 into 90 g lactic acid l−1 in less than 40 h (Adsul et al. 2007), and, with the addition of cellulase, 80 g cellulose l−1 into 67 g lactic acid l−1 in about 80 h (Adsul et al., 2006). The strain converted cellotriose and higher cellooligosaccharides, too, though at lower specific rates. Thermotolerant Bacillus strains described below are particularly suited to SSF because they were specifically isolated for their ability to generate lactic acid at 50 °C or above. For example, B. coagulans 36D1 generated 80 g lactic acid l−1 from 100 g cellulose l−1 during the course of 264 h when supplemented with cellulase (Ou et al. 2011).
Waste materials are also common substrates for the production of lactic acid using SSF. For example, cardboard subject to enzymatic hydrolysis is a source for lactic acid production by Lactobacillus coryneformis ssp. torquens (Yáñez et al. 2005). In a fed-batch process, 23.4 g lactic acid l−1 was generated at a 0.51 g/g yield from glucose at a volumetric productivity of 0.48 g l−1 h−1. Using the same strain, d-lactic acid production from filter paper was also studied in an SSF. This process showed better yield when cellobiase was added externally, reaching about 25 g lactic acid l−1 in 48 h with a yield of 0.72 g lactic acid/g cellulose (Yáñez et al. 2003). The improvement in yield in cellulose compared with glucose as a substrate suggests that the slow release of glucose favors lactic acid formation over biomass production. d-Lactic acid production has also been studied from defatted rice bran which was not subject to sterilization (Tanaka et al. 2006). Because the indigenous bacteria produced a racemic mixture of lactic acid, the pH was maintained at 5 to ensure only d-lactic acid production by the intended Lb. delbrueckii. About 30 g lactate l−1 at a yield of 0.28 g lactic acid/g rice bran or 0.78 g lactic acid/g soluble sugars was achieved. Recycled paper sludge generated 73 g lactic acid l−1 using Lb. rhamnosus in a culture supplemented with cellulolytic and xylanolytic enzymes (Marques et al. 2008).
A challenge in SSF is matching the optimal conditions for enzymatic saccharification with the optimal conditions for microbial conversion (e.g., temperature, pH). Thus, in the case of lactic acid accumulation via SSF, many researchers have sought to increase the tolerance to temperature and pH of the lactic acid-producing microbes (described below). John and Nampoothiri (2008) applied classical mutagenesis using nitrous oxide to Lb. delbrueckii to obtain two mutants, which in SSF of cassava bagasse starch hydrolysate, generated lactate at a yield > 90 % while the wild-type generated lactate at a yield of about 50 %.
Mixed cultures for lactic acid formation
Several studies have proposed the use of mixed cultures of microbes, wherein each microbe selected for the microbial consortium accomplishes one specific conversion. Such an approach can address one of several specific objectives, but in each case the two or more organisms comprising the culture must be compatible and have similar nutritional and environmental requirements.
One application of mixed cultures is based on the concept that some microbes very effectively convert glucose into lactic acid, while others may be effective at the conversion of pentoses into lactic acid. For example, a homofermentative strain will attain a higher yield from glucose because it relies on the EMP pathway, while a heterofermentative LAB will generate more ATP from pentoses through the PK pathway and thus can generate lactate with high productivity though some yield is sacrificed. Based on this rationale, a mixed culture of Lb. rhamnosus (homofermenter) and Lb. brevis (heterofermenter) has been studied. This culture will generate lactic acid from a xylose/glucose mixture or from a corn stover hydrolysate to which cellulase was added (Cui et al. 2011). Using two strains led to higher overall lactate yield and productivity (0.7 g/g and 0.59 g l−1 h−1) compared with using only the homofermenter (0.59 g/g and 0.49 g l−1 h−1). The selection of strains is important for the efficient conversion of sugar mixtures.
Another application of mixed cultures is accomplishing a two-organism SSF: one microbe saccharifies the biomass while a second ferments the hydrolysate. For example, Lactobacillus ssp. and Aspergillus niger converted Jerusalem artichoke tubers into L-lactic acid (Ge et al. 2009). In this case, A. niger generated inulinase and invertase to hydrolyze the inulin to glucose, and Lactobacillus inoculation was delayed 12 h to allow for some glucose accumulation. Interestingly, the presence of Lactobacillus increased enzyme production by A. niger, presumably because of the removal of glucose from the culture. The system achieved approx. 120 g l-lactic acid l−1 with a yield of 0.945 g/g in a repeated-batch process.
A third and different application of mixed cultures involves using a consortium of engineered strains to convert sugar mixtures into lactic acid (Eiteman et al. 2009). For example, for the conversion of xylose and glucose, the strategy uses two strains: one unable to consume glucose, and one unable to consume xylose. When both strains were conferred with additional knockouts for lactate generation, each member of the mixture carried out the one conversion. Such a system adapts to a changing xylose/glucose composition by changing the relative population of each strain (Eiteman et al. 2008), and thus very effectively converts mixed sugar streams into products such as lactic acid (Eiteman et al. 2009).
Lower metabolism involved in lactic acid formation
One common challenge for the production of lactic acid is that numerous by-products can be generated, depending on the microbe used and the pathways that microbe possesses. Different LAB, particularly, express several enzymes which compete with LDH for the utilization of pyruvate. The LDHs present in an organism and their catalytic efficiency also determine the relative abundance of the two isomers in the product (Zheng et al. 2012). Furthermore, several paralogs show some l-LDH or d-LDH activity and reduce the optical purity of lactic acid (Rico et al. 2008). Figure 2 shows enzymes found in lower metabolism of several LAB associated with pyruvate and acetate-P, the products of the EMP, PP pathways and PK pathways. Different organisms have other competing pathways, the importance of which also depends on the starting carbon source used. Reducing by-product formation has been a consistent theme in studying lactic acid production by many bacteria and fungi.
Decrease of by-products formed from glucose
As a model organism which is easy to manipulate genetically, E. coli accumulates significant lactic acid from glucose by simply knocking out the pflB gene coding pyruvate formate lyase (Dien et al. 2001; Dien et al. 2002). Though E. coli predominantly generates the D-lactate isomer, it may readily be turned into an l-lactate producer by knocking out the native gene coding d-LDH (ldhA) and a gene coding for an l-LDH (Chang et al. 1999; Dien et al. 2002; Zhou et al. 2004). Often a “two-phase” process is implemented to accumulate lactic acid, whereby an aerobic growth phase is decoupled from a subsequent anaerobic or microaerobic phase leading to lactate production. A two-phase approach is indeed necessitated by the knockout of the pflB gene, or any other gene which curtails anaerobic cell growth. Advantages of a two-phase process are higher yields because no carbon is converted to biomass during the non-growth production phase, and greater tolerance to environmental conditions during lactate accumulation because cell growth is not actually required.
Many studies have focused on this strategy. For example, a pflB knockout overexpressing the Streptococcus bovis ldh gene generated 73 g l-lactic acid l−1 on a complex medium at a yield of 0.93 g/g (Dien et al. 2001). A strain with knockouts in pyruvate formate lyase, fumarate reductase (frdBC), alcohol dehydrogenase (adhE) and acetate kinase (ackA) grown in defined medium generated 48 g lactate l−1 of 99 % optical purity close to the theoretical maximum yield of 1 g/g (Zhou et al. 2003), and then replacing the chromosomal ldhA with an l-LDH gene led to 50 g L-lactate l−1 at a yield of 0.95 g/g (Zhou et al. 2004). In an acetate-auxotroph having knockouts in pyruvate dehydrogenase (aceEF), pyruvate oxidase (poxB), PEP synthase (pps) and pyruvate formate lyase, all which compete with LDH for pyruvate, E. coli generated over 90 g lactate l−1 with a yield of 0.95 g/g with succinate as the single by-product (Zhu et al. 2007). Additionally knocking out frdABCD coding fumarate reductase, and ensuring that the co-substrate acetate was absent at the time the anaerobic phase commences led to 138 g lactate l−1 in defined medium with a yield of 0.99 g/g and less than 1 % by-products (Zhu et al. 2007). A similar set of knockouts has been scaled up to 3,000 liters and demonstrated the benefit of Ca(OH)2 as the neutralizing agent (Liu et al. 2014). Other combinations of knockouts which decrease by-product formation have also been studied. For example, a phosphotransferase (pta) and PEP carboxylase (ppc) mutant generated 62 g d-lactate l−1 on a complex medium with a yield of 0.9 g/g (Chang et al. 1999), while knocking out the native d-LDH and expressing l-LDH from Lactobacilllus casei generated 45 g l-lactate l−1 with a yield of 0.7 g/g (Chang et al. 1999).
Corynebacterium glutamicum, used commercially for amino acid production, has recently been examined for lactic acid production. With a native l-LDH, C. glutamicum needs a knockout in this l-LDH and overexpression of d-LDH from Lb. delbrueckii to accumulate d-lactate from glucose. After aerobic cell growth, centrifuged, washed and resuspended cells (at 60 g l−1) with repeated glucose addition accumulated 120 g d-lactate l−1 in 30 h in a high density resting cell approach (Okino et al. 2008). The system also accumulated 17 g succinate l−1 and less acetate. Klebsiella ssp. have also been examined for the production of lactic acid from glucose. Klebsiella oxytoca with knockouts in phosphotransacetylase, acetate kinase and alcohol dehydrogenase generated 13 g d-lactic acid l−1 from 20 g glucose l−1, and also generated 24 g d-lactic acid l−1 from sugarcane molasses in 96 h (Sangproo et al. 2012).
There has long been an interest in using yeast, particularly Saccharomyces cerevisiae, for the production of lactic acid from glucose (Dequin and Barre 1994; Porro et al. 1995). The motivation is that S. cerevisiae tolerates a low pH of about 3.5 and is efficient at the conversion of glucose to ethanol through the EMP pathway at nearly theoretical yield. Therefore, although S. cerevisiae is naturally an ethanol producer, the microbe might similarly be able to accumulate the redox-neutral product, lactic acid, if ethanol formation were to be prevented. For example, a knockout in one of the pyruvate decarboxylase genes involved in ethanol generation (PDC1) and overexpressing the bovine ldh gene (via a plasmid) led to a lactate yield of 0.20 g/g and an ethanol yield of 0.26 g/g, though cell growth was repressed (Adachi et al. 1998). More recently, PDC1 was similarly knocked out and two copies of the ldh gene from Leuconostoc mesenteroides integrated onto the S. cerevisiae chromosome (Ishida et al. 2006a). From 100 g glucose l−1, this yeast strain generated about 62 g d-lactate l−1 when the pH was controlled and about 53 g d-lactate l−1 without pH control (final pH was 2.8). Knocking out both PDC1 and PDC5 and integrating two copies of the bovine ldh gene led to over 82 g l-lactate l−1 in 200 h at a yield of 0.815 g/g glucose (Ishida et al. 2006b). More recently, strains with single gene disruptions were screened to find strains with improved resistance to L-lactic acid at a pH of 2.6 (Suzuki et al. 2013). Overexpressing l-LDH in a PDC1 knockout strain with four additional gene disruptions (DSE2 SCW11 EOF3 SED1) led to 48 g l-lactic acid l−1 compared to 38 g l−1 in the strain overexpressing the l-LDH in a PDC1 knockout. Each of these recent studies used a medium containing 10 g yeast extract l−1 and 20 g peptone l−1.
Saccharomyces cerevisiae is not the only yeast used for generating lactic acid from glucose, but by-products must invariably be eliminated and lactic acid formation enhanced. Kluyveromyces marxianus strains were constructed with the Lactobacillus helveticus L-LDH gene using phosphoglycerate kinase and pyruvate decarboxylase promoters at various points in the chromosome (Hause et al. 2009). With CaCO3 added for pH control and deleting the native single copy of pyruvate decarboxylase (PDC1), K. marxianus generated about 99 g l-lactate l−1 (> 99 % enantiomerically pure) from 104 g glucose l−1 in 48 h without any ethanol production. This strain also generated 9.1 g lactate l−1 from 10.8 g glucose l−1 after 72 h without pH control, which led to a final pH of about 3. Similarly, Candida boidinii expressing codon-optimized bovine L-LDH using the PDC1 promoter in a PDC1 knockout resulted in about 86 g lactate l−1 in 48 h at a yield of 1 g/g glucose (Osawa et al. 2009). By knocking out PDC1 and introducing two L-LDH genes derived from Bos taurus under the control of the PDC1 promoter, C. boidinii was able to generate over 100 g l-lactic acid l−1 in 33 h (Ikushima et al. 2009).
A series of patents have been issued for the production of lactic acid in yeast. For example, with a goal of producing lactic acid at a low pH so that base consumption is minimized and the acid form (i.e., lactic acid) predominates, several yeasts with knockouts in the pyruvate dehydrogenase complex and pyruvate decarboxylase were transformed with one or more copies of the LDH gene and a lactate transporter (Porro et al. 2006). The researchers noted that a higher concentration and productivity of lactic acid can be attained in a medium having a low concentration of Mg2+ or Zn2+ ions. Lactic acid will also accumulate using yeast variants which have temperature-sensitive alcohol dehydrogenase or pyruvate decarboxylase and which express human- or frog-LDH (Sawaii et al. 2011).
Issatachenkia orientalis has been developed for lactic acid production because this yeast tolerates a pH below 3 (Suominen et al. 2012; Miller et al. 2012). With knockouts in native pyruvate decarboxylase and lactate:ferricytochrome c oxidoreductase genes and overexpressing one or more copies of l-LDH, this yeast generated 60 g lactate l−1 at a yield of 0.6 g/g under microaerobic conditions.
Decrease of by-products from pentoses
Most of the same knockouts involved in the conversion of glucose to lactic acid apply also when pentoses are the substrates. For example, E. coli with essentially the same knockouts as described above to exclude by-products, as well as containing the chromosomally-integrated Pediococcus acidilactici l-LDH gene (ldhL), generated 42.9 g l-lactic acid l−1 from xylose under anaerobic conditions in about 120 h in a defined medium (Zhao et al. 2013). Candida utilis expressing xylitol dehydrogenase, xylulokinase and a xylose reductase mutated to favor NAD over NADP+ generated 67 g l-lactate l−1 from xylose in 72 h (Tamakawa et al. 2012). The yeast Pichia stipitis is advantageous because it naturally ferments xylose, primarily to ethanol (Prior et al. 1989). Using P. stipitis with an l-LDH gene from Lb. helveticus expressed under the control of the ADH1 promoter led to 58 g L-lactate l−1 from 100 g xylose l−1 or 41 g lactate l−1 from 94 g glucose l−1 (Ilmén et al. 2007). The lower production of lactate from glucose was attributed to the greater ethanol formation from this substrate. Despite the presence of an intact pyruvate-to-ethanol pathway, the cells generated 70 % less ethanol from xylose with ldhL expression. Interestingly, this P. stipitis construct was able to metabolize glucose and xylose simultaneously.
Decrease of by-products from glycerol
Glycerol has also been used as a substrate for lactic acid production by E. coli (Mazumdar et al. 2010). By overexpressing enzymes involved in the conversion of glycerol to dihydroxyacetone phosphate, and knocking out fumarate reductase (frdA), phosphotransferase (pta), alcohol dehydrogenase (adhE) and respiratory d-lactate dehydrogenase (dld) genes, 32 g d-lactate l−1 was generated from 40 g glycerol l−1 in about 72 h in shake-flasks. Modifying the E. coli strain by replacing the native d-LDH with an l-LDH, blocking the methylglyoxal pathway, and preventing reassimilation of L-lactate by eliminating a native aerobic l-LDH led to 50 g l-lactate l−1 with 99.9 % optical purity from 56 g crude glycerol l−1 in 84 h (Mazumdar et al. 2013). An economic assessment of the conversion of glycerol to d-lactic acid by engineered E. coli indicated that the use of crude glycerol represents less than 8 % of the production cost, and that the process could be a profitable use for glycerol (Posada et al. 2012). Moreover, the success of the conversion depends mostly on the fermentation, and in particular the ability of strains to convert completely high concentrations of glycerol. Another approach involves the typical two-phase process: using a two-phase approach without overexpression of genes involved in glycerol uptake, E. coli was able to generate 99 g d-lactate l−1 in 36 h at a yield of 0.64 g/g (Tian et al. 2012; Chen et al. 2014). Overexpression of ldhA increased final concentration and yield. Importantly, a two-phase approach allows different environmental conditions: for example, E. coli growth is favored at 34–37 °C, while anaerobic conversion of glycerol into lactic acid favors 40 °C (Chen et al. 2014). The use of crude glycerol compared to purified glycerol does not appear to impact the production of lactic acid (Chen et al. 2014), although methanol present as high as 28 % (w/w) is largely lost on autoclaving (Pyle et al. 2008).
Wild-type Klebsiella pneumoniae generates a surprisingly high concentration of d-lactic acid when subject to microaerobic conditions and high glycerol feed rates (Rossi et al. 2013). If one thus accepts the generation of by-products, the organism is suitable for the co-production of 1,3-propanediol and d-lactic acid, which may readily be separated from each other (Song et al. 2013). Knocking out just two genes leading to 1,3-propanediol (dhaT and yqhD) and overexpressing a d-LDH led to 142 g d-lactic acid l−1 at a yield of 0.82 g/g glycerol (Feng et al. 2014). The availability of some oxygen under microaerobic conditions appears to be critical in maximizing d-lactic acid formation in K. pneumoniae (Feng et al. 2014).
Membrane transport associated with lactate formation
In many cells glucose is transported across the cell membrane via a sugar-specific phosphotransferase system (PTS), though variations in this strategy exist. Lc. lactis transports glucose via a mannose-PTS, a cellobiose-PTS (rather than a glucose-PTS) and a unique glucose permease (Castro et al. 2009). The concentration of phosphate can play an important role in the regulation of glycolysis (e.g., Lc. lactis), with low phosphate inhibiting glycolysis particularly at high glucose concentrations (Levering et al. 2012). Xylose transport in several Lactobacillus spp. occurs via facilitated diffusion (Chaillou et al. 1998, 1999), while in E. coli xylose uptake occurs by both high-affinity (ATP-dependent) and low-affinity (ATP-independent) routes (Sumiya et al. 1995).
Saccharomyces cerevisiae appears to be limited in the efflux of lactate, and two monocarboxylate permeases, Jen1 and Ady2, play an important role in lactate export from the cell (Pacheco et al. 2012), though Ady2 is considered an acetate permease (Paiva et al. 2004). A knockout in both JEN1 and ADY2 significantly reduced consumption of lactic acid from the medium after the glucose had been exhausted while the overexpression of JEN1 and ADY2 increased lactic acid production but also increased lactic acid utilization after glucose exhaustion. Thus, these enzymes are involved in bidirectional lactic acid uptake and efflux (Pacheco et al. 2012). A mutation in the ADY2 gene has also been linked to increased lactate efflux through laboratory evolution (de Kok et al. 2012). Although the quantity of lactic acid generated varies widely depending on the strain of yeast used (Branduardi et al. 2006), these earlier studies generated less than 0.5 g lactic acid/l (Pacheco et al. 2012). An almost doubling of lactate yield to 0.75 g/g glucose under continuous culture conditions led to speculation that this operational mode may be advantageous for lactic acid production by S. cerevisiae because such a process maintains a very low glucose concentration and thus reduces the Crabtree effect found in this yeast (Mimitsuda et al. 2014).
Compared to research involving upper or lower metabolism, relatively little research has investigated improving lactate production through the alteration of native sugar or lactate transport into or out of the cell.
Increasing microbial tolerance
Microbial processes for lactic acid generation are commonly limited by the tolerance of production organisms to extreme conditions of pH or temperature, as well to elevated sugar and lactic acid concentrations. Furthermore, inhibitors present in the biomass hydrolysates and other inexpensive materials which are attractive for lactic acid production can hinder growth and product formation. Therefore, the selection and improvement of strains for tolerance to certain environmental conditions are key aspects in process development for large scale cultivation. Two general strategies have been adopted for obtaining more tolerant microbial strains. One method involves improving known lactic acid producers by various evolutionary techniques such as random mutagenesis or genome shuffling. A second method is to establish first what characteristics are needed in a production microbe, and then isolate microbes from the natural environment which satisfy those characteristics. Lactic acid production is then subsequently introduced or improved in those isolates.
Tolerance to low pH
During microbial generation of lactic acid from simple sugars such as glucose, the pH of the culture will decrease. Microbes are often inhibited by lowered pH, leading to a reduction and ultimately a cessation of cell growth and further lactic acid formation. This pH-dependent inhibition necessitates the use of strong base to neutralize the accumulating acid during the course of the fermentation. However, the use of bases such as NaOH, KOH or Ca(OH)2 is accompanied by its own drawbacks. In particular, the cells may be inhibited by the increased concentration of a neutralizing counter-cation (e.g., Na+), and additional processing steps are required to remove the counterion and leave the ultimate acid product. So, two approaches have been explored to resolve the problem of decreasing pH during a lactic acid fermentation, including increasing microbial tolerance to cations and increasing microbial tolerance to low pH.
Several researchers have increased tolerance to cations in microbes able to generate more lactate. Applying the hypothesis that Na+ might limit lactic acid production, a 25 % increase in lactate accumulation (70 vs. 56 g l−1) was reported in an E. coli strain overexpressing Na+-specific regulator gene nhaR and the nhaA gene expressing the Na+/H+ antiporter membrane protein (Wu et al. 2013a). Similarly, overexpressing the DNA repair protein RecO in L. casei led to a 40 % increase in lactic acid concentration under NaCl stress, although the lactic acid concentrations accumulated were less than 5 g l−1 (Wu et al. 2013b). Subjecting a Bacillus isolate to low energy ions generated a mutant more tolerant to Na+ which at 50 °C was able to convert glucose to over 100 g l-lactate l−1 with productivities exceeding 3.5 g l−1 h−1 (Qin et al. 2010). E. coli merely exposed to progressively increasing concentrations of Na+ showed greater tolerance to both Na+ and K+ ions and, when conferred with a single knockout in the pflB gene, showed a 35 % increase in lactic acid production (76 g l−1) compared to the wild-type strain (Wu et al. 2014).
Lactic acid-producing bacteria may similarly be adapted to greater acid tolerance. Just one round of whole genome shuffling on Lb. pentosus was necessary to generate transformants with improved growth at a pH of 4 (Ye et al. 2013a). One mutant, MT3, produced lactic acid at 95 % yield from 20 g glucose l−1 at a pH of 3.8. These authors did not identify the altered genes nor the mechanism for the increased acid tolerance but the mutation did not have any effect on lactate synthesis. Increased acid tolerance of Lb. rhamnosus was also achieved by genome shuffling using two UV mutants and three nitrosoguanidine mutants as the template strains (Wang et al. 2007). At a controlled pH of 4.5, the ultimate strain was able to generate about 84 g l−1 after an 84 h fermentation. Similarly, Sporolactobacillus inulinus was subject to UV irradiation and diethyl sulfate mutagenesis to generate starting populations for genome shuffling, which led to a strain resistant to a pH of 5 that generated 93 g d-lactic acid l−1 from glucose in complex medium (Zheng et al. 2010). Interestingly, a pH-tolerant mutant of Lb. casei showed greater PTS activity, greater H+-ATPase activity and, at lower values of pH, maintained a higher intracellular pH than the wild-type, with a subsequent proteomic analysis demonstrating the complexity of pH tolerance (Wu et al. 2012). The response of LAB to low pH involves surprisingly numerous genes or proteins (Rallu et al. 2000; De Angelis et al. 2001).
A source to isolate new acid-tolerant bacteria is the corn-processing facilities themselves. Acid-tolerant bacteria which produce lactic acid at a pH of 4.2 or less have been isolated directly from industrial wet mills (Carlson and Peters 2002), and then subsequently examined for the effect of temperature, SO2, and steep-water on their growth. Similarly, bacteria were isolated from corn-steep liquor producing L-lactic acid (Eddington et al. 2007), and six Lactobacilli were identified. These strains each generated over 80 g l-lactic acid l−1 with 96 % optical purity and a yield over 80 % in 50 h. After chemical mutagenesis, the strains were examined for the absence of d-lactic acid. In this way, strains able to generate exclusively l-lactic acid at high yield and final concentration were also generated.
Tolerance to elevated temperatures
Increased tolerance to elevated temperature is also desirable for potentially increasing productivity and for reducing the prospect of contamination. To increase thermotolerance of Lb. casei, a mutant was selected by isolating for growth at progressively higher temperatures and glucose concentrations (Ge et al. 2011). The resulting mutant, named G-03, generated lactate maximally at 41 °C, whereas the parent strain generated maximal lactate at 34 °C. G-03 generated over 198 g lactate l−1 at 41 °C, approximately twice the concentration and productivity of the parent strain.
Thermotolerant strains have been isolated directly from the environment. For example, Qin et al. (2009) selected Bacillus 2-6 from 730 soil isolates that grew at 55 °C, and Bischoff et al. (2010) isolated 40 strains on a xylose-containing complex medium at 50 °C, and 16S rDNA showed all were B. coagulans. Demonstrating the advantage that high temperature provides against contamination, Bacillus 2–6 generated 182 g l-lactic acid l−1 in a medium of 20 g yeast extract l−1 in a 30 l fed-batch process without sterilization (Qin et al. 2009) into which glucose was fed continuously. Bacillus 2–6 also generated 60–100 g l-lactic acid l−1 with over 99 % optical purity in repeated batch fermentations at an average of 0.9 g/g yield and productivities exceeding 1 g l−1 h−1, though production was very dependent on yeast extract concentration (Zhao et al. 2010). During batch fermentation of 120 g xylose l−1, thermotolerant isolate B. coagulans NL01 generated 80 g l-lactate l−1 in 72 h (Ouyang et al. 2012), while B. coagulans C106 generated 216 g from xylose l−1 during a fed-batch process (Ye et al. 2013b). Otto (2012) describe thermophilic strains (56 °C) of B. coagulans and Geobacter also tolerant to a pH of 5.6. Immobilization of a thermotolerant Bacillus extends the productivity of the process: approx. 70 g lactic acid l−1 from 80 g/l glucose during each of fifteen repeated fed-batch fermentations (Rosenberg et al. 2005). All these recent studies using Bacillus strains confirm research from a decade earlier demostrating lactic acid production by thermotolerant Bacillus spp. (Heriban et al. 1993; Ohara and Yahata 1996; Payot et al. 1999).
A few species other than Bacillus have been isolated from the environment for their thermotolerance. For example, an L. delbrueckii strain isolated from a sink tolerated 50 °C. Using continuous culture with membrane recycle at 43 °C, this strain generated 20 g d-lactic acid l−1 continuously from 20 g glucose l−1 at a productivity of 18 g l−1 h−1 and a yield of 1 g/g (Tashiro et al. 2011). In batch culture 87.4 g d-lactic acid l−1 accumulated in 168 h from 100 g glucose l−1. However, B. coagulans is advantageous compared to Lb. delbrueckii in terms of higher operational temperature, productivity and simplicity of medium requirements (Michelson et al. 2006).
Tolerance to elevated sugar concentration
Increased tolerance to high sugar concentrations or increased generation of lactic acid are worthy targets for random mutation. Lb. lactis was mutated with UV and selecting for increased acid production by strains having a larger acid zone on plate (Joshi et al. 2010). Two additional rounds of UV irradiation led to strain RM2-24, which generated 120 g lactic acid l−1 from 200 g hydrolyzed cane sugar l−1 in 120 h. Genome shuffling to increase the glucose tolerance of Lb. rhamnosus resulted in a strain which generated 180 g l-lactic acid l−1 from 200 g glucose l−1 in 90 h (Yu et al. 2008).
Tolerance to multiple stresses
Strategies have also been used to obtain strains with increased tolerance to multiple stresses. For example, Patel et al. (2006) isolated many microbes from a wide range of sources, and selected strains which could ferment sugars in sugar cane bagasse hydrolysate at a pH of 5 and 50 °C, conditions which match conditions necessary for cellulase activity and would reduce the need for sterilization and require less cooling. Three strains of B. coagulans generating lactic acid as the major anaerobic product were isolated, and strain 36D1 has been the subject of continuing research. B. coagulans 36D1 generated over 150 g lactic acid l−1 from either 200 g glucose l−1 or 200 g xylose l−1 in about 200 h (Ou et al. 2011). Similarly, Rallu et al. (2000) obtained 21 insertional mutants of Lc. lactis from a combination of low pH, elevated temperature and aerobic conditions. The researchers classified these mutants into four classes and concluded that acid tolerance is a complex process which involves phosphate and purine nucleotide pools and multiple transporters.
Heterologous expression of nisin-induced dnaK from E. coli in Lc. lactis improves tolerance to heat, salt and ethanol stress, particularly at 40 °C (Al-Mahin et al. 2010), though the concentrations of lactic acid were low (1–2 g l−1). DnaK is believed to transduce signals to other cellular factors in response to increased temperature, and also to plays a role in refolding of thermally damaged proteins.
Further research on tolerant strains
Research has progressed to decrease by-product formation in some tolerant strains, or to use these strains directly for the conversion of lignocellulosic hydrolysates. For example, thermotolerant B. coagulans P4-102B with knockouts in the native l-LDH (ldh) and acetolactate synthase (alsS) genes, regains anaerobic growth after a mutation in glycerol dehydrogenase (gldA) causes the enzyme to act as a d-LDH, resulting in 90 g d-lactate l−1 from glucose after 48 h (Wang et al. 2011). Interestingly, for B. coagulans NL01 both acetate and levulinate exhibited a toxic effect, while 2 g formate l−1 showed a stimulatory effect, and in corn stover hydrolysate this strain consumed xylose, arabinose and glucose simultaneously (Ouyang et al. 2012). B. coagulans MXL-9 grew on a synthetic mixture of 17 g l−1 each of glucose, xylose and arabinose, resulting in about 90 % yield on the three sugars after 36 h in the pH range of 6–6.5 (Bischoff et al. 2010). MXL-9 showed a 50 % decrease in OD after 24 h with 2.5–5 g furfural l−1 and 5-HMF, but was nevertheless able to ferment corn fiber hydrolysates without overliming to over 40 g lactic acid l−1. Bacillus XZL9, which was isolated specifically for l-lactic acid formation from xylose at 50 °C, generated 134 g l-lactic acid l−1 in 218 h in a fed-batch fermentation, and about 74 g l-lactic acid l−1 from corncob molasses (Wang et al. 2010b). Lactate-generating fungi have also been the subject of strain improvement: subjecting R. oryzae to low energy ions led to mutants with increased metabolism of both xylose and glucose to 80 g lactic acid l−1 in 70 h, although the rate of xylose conversion remained much slower than the rate of glucose conversion (Wang et al. 2009).
The microbial production of lactic acid is a maturing technology which has, for over a decade, been successfully commercialized by several companies. With a current production cost on the order of a dollar per kg (Posada et al. 2012), even the highest producing strains generate a culture having lactic acid valued at less than $0.25 per liter. At such a low value for the fermentation product, the cost of the medium and operating conditions become critical in achieving an economic target for lactic acid production. Significant improvements have been achieved by isolating new microbes, or enhancing existing microbes for greater tolerance to high temperature and low pH in order to reduce contamination and operational costs. Nevertheless, the practical goal of improving microbe characteristics should be accompanied by a fundamental understanding of how cells response to such environments (e.g., membrane integrity, lactate transport, enzyme stability). Bioinformatic tools, for example, though rarely applied for lactic acid production, could provide better enzymes and processes. With the consistent desirability for using inexpensive agriculturally-generated residues, and reducing the cost of the medium, research should continue to provide scalable understanding into cellular responses to such substrates. Research on bioreactor operational modes, such as nutrient-limited (N, P, etc.) fed-batch processes, could not only provide further insights into cellular responses to environmental conditions, but could make significant improvements in lactic acid productivity, yield and final concentration.
Adachi E, Torigoe M, Sugiyama M, Nikawa JI, Shimizu K (1998) Modification of metabolic pathways of Saccharomyces cerevisiae by the expression of lactate dehydrogenase and deletion of pyruvate decarboxylase genes for the lactic acid fermentation at low pH value. J Ferment Bioeng 86:284–289
Adsul MG, Varma AJ, Gokhale DV (2006) Lactic acid production from waste sugarcane bagasse derived cellulose. Green Chem 9:58–62
Adsul MG, Khire J, Bastawde K, Gokhale D (2007) Production of lactic acid from cellobiose and cellotriose by Lactobacillus delbrueckii mutant Uc-3. Appl Environ Microbiol 73:5055–5057
Al-Mahin A, Sugimoto S, Higashi C, Matsumoto S, Sonomoto K (2010) Improvement of multiple-stress tolerance and lactic acid production in Lactococcus lactis NZ9000 under conditions of thermal stress by heterologous expression of Escherichia coli dnaK. Appl Environ Microbiol 76:4277–4285
Bai DM, Li SZ, Liu ZL, Cui ZF (2008) Enhanced L-(+)-lactic acid production by an adapted strain of Rhizopus oryzae using corncob hydrolysate. Appl Biochem Biotechnol 144:79–85
Bischoff KM, Liu S, Hughes SR, Rich JO (2010) Fermentation of corn fiber hydrolysate to lactic acid by the moderate thermophilic Bacillus coagulans. Biotechnol Lett 32:823–828
Blomqvist J (2001) RIS Metropolis Monte Carlo studies of poly(lactic), poly(L, D-lactic) and polyglycolic acids. Polymer 42:3515–3521
Branduardi P, Sauer M, De Gioia L, Zamella G, Valli M, Mattanovich D, Porro D (2006) Lactate production yield from engineered yeasts is dependent from the host background, the lactate dehydrogenase source and the lactate export. Microb Cell Fact 5:4
Carlson TL, Peters EM, Jr. (2002) Low pH lactic acid fermentation. US Patent 6,475,759, 5 Nov 2002
Castro R, Neves AR, Fonseca LL, Pool WA, Kok J, Kuipers OP, Santos H (2009) Characterization of the individual glucose uptake systems of Lactococcus lactis: mannose-PTS, cellobiose-PTS and the novel GlcU permease. Mol Microbiol 71:795–806
Chaillou S, Bor YC, Batt CA, Postma PW, Pouwels PH (1998) Molecular cloning and functional expression in Lactobacillus plantarum 80 of xylT, encoding the D-xylose-H + symporter of Lactobacillus brevis. Appl Environ Microbiol 64:4720–4728
Chaillou S, Pouwels PH, Postma PW (1999) Transport of D-xylose in Lactobacillus pentosus, Lactobacillus casei, and Lactobacillus plantarum: evidence of a mechanism of facilitated diffusion via the phosphoenolpyruvate:mannose phosphotransferase system. J Bacteriol 181:4768–4773
Chang DE, Jung HC, Rhee JS, Pan JG (1999) Homofermentative production of D- or L-lactate in metabolically engineered Escherichia coli RR1. Appl Environ Microbiol 65:1384–1389
Chen XZ, Tian KM, Niu DD, Shen W, Algasan G, Singh S, Wang ZX (2014) Efficient bioconversion of crude glycerol from biodiesel to optically pure D-lactate by metabolically engineered Escherichia coli. Green Chem 16:342–350
Cui F, Li Y, Wan C (2011) Lactic acid production from corn stover using mixed cultures of Lactobacillus rhamnosus and Lactobacillus brevis. Biores Technol 102:1831–1836
Datta R, Henry M (2006) Lactic acid: recent advances in products, process, and technologies: a review. J Chem Technol Biotechnol 81:1119–1129
De Angelis M, Bini L, Pallini V, Cocconcelli PS, Gobbetti M (2001) The acid-stress response in Lactobacillus sanfranciscensis CB1. Microbiology 147:1863–1873
de Jong SJ, van Eerdenbrugh B, van Nostrum CF, Kettenes-van de Bosch JJ, Hennink WE (2001) Physically crosslinked dextran hydrogels stereocomplex formation of lactic acid oligomers: degradation and protein release behavior. J Contr Rel 71:261–275
de Kok S, Nijkamp JF, Oud B, Roque FC, de Ridder D, Daran JM, Pronk JT, van Maris AJA (2012) Laboratory evolution of new lactate transporter gene in a jen1Δ mutant of Saccharomyces cerevisiae and their identification as ADY2 alleles by whole-genome resequencing and transcriptome analysis. FEMS Yeast Res 12:359–374
Dequin S, Barre P (1994) Mixed lactic acid-alcoholic fermentation by Saccharomyces cerevisiae expressing the Lactobacillus casei L(+)-LDH. Nature Biotechnol 12:173–177
Dien BS, Nichols NN, Bothast RJ (2001) Recombinant Escherichia coli engineered for production of L-lactic acid from hexose and pentose sugars. J Ind Microbiol Biotechnol 27:259–264
Dien BS, Nichols NN, Bothast RJ (2002) Fermentation of sugar mixtures using Escherichia coli catabolite repression mutants engineered for production of L-lactic acid. J Ind Microbiol Biotechnol 29:221–227
Drumright RE, Gruber PR, Henton DE (2000) Polylactic acid technology. Adv Mater 12:1841–1846
Eddington JM, Johnson KB, Liaw HJ, Rowe M, Yang Y (2007) Lactobacillus strains and use thereof in fermentation for L-lactic acid production. US Patent 7,300,787, 27 Nov 2007
Eiteman MA, Lee SA, Altman E (2008) A co-fermentation strategy to consume sugar mixtures effectively. J Biol Eng 2:3
Eiteman MA, Lee SA, Altman R, Altman E (2009) A substrate-selective co-fermentation strategy with Escherichia coli produces lactate by simultaneously consuming xylose and glucose. Biotechnol Bioeng 102:822–827
Feng X, Ding Y, Xian M, Xu X, Zhang R, Zhao G (2014) Production of optically pure D-lactate from glycerol by engineered Klebsiella pneumoniae strains. Biores Technol 172:269–275
Gao C, Ma C, Xu P (2011) Biotechnological routes based on lactic acid production from biomass. Biotechnol Adv 29:930–939
Ge XY, Qian H, Zhang WG (2009) Improvement of L-lactic acid production from Jerusalem artichoke tubers by mixed culture of Aspergillus niger and Lactobacillus sp. Biores Technol 100:1872–1974
Ge XY, Yuan J, Qin H, Zhang WG (2011) Improvement of L-lactic acid production by osmotic-tolerant mutant of Lactobacillus casei at high temperature. Appl Microbiol Biotechnol 89:73–78
Gruber PR, Hall ES, Kolstad JJ, Iwen ML, Benson RD, Borchadt RL (1992) Continuous process for manufacture of lactide polymers with controlled optical purity. US Patent 5,142,023, 25 Aug 1992
Gruber PR, Kolstad JJ, Ryan CM, Hall ES, Eichen Conn RS (1996) Meta-stable amorphsus lactide polymer film and process for manufacturing thereof. US Patent 5,484,881, 16 Jan 1996
Guo W, Jia W, Chen S (2010a) Performances of Lactobacillus brevis for producing lactic acid from hydrolysate of lignocellulosics. Appl Biochem Biotechnol 161:124–136
Guo Y, Yan Q, Jiang Z, Teng C, Wang X (2010b) Efficient production of lactic acid from sucrose and corncob hydrolysate by a newly isolated Rhizopus oryzae GY18. J Ind Microbiol Biotechnol 37:1137–1143
Hause B, Rajgarhia V, Suominen P (2009) Methods and materials for the production of L-lactic acid in yeast. US Patent 7,534,597, 19 May 2009
Heriban V, Šterdík E, Zalibera L, Matuš P (1993) Process and metabolic characteristics of Bacillus coagulans as a lactic acid producer. Lett Appl Microbiol 16:243–246
Hofvendahl K, Hahn-Hägerdal B (2000) Factors affecting the fermentative lactic acid production from renewable resources. Enz Microb Technol 26:87–107
Ikushima S, Fujii T, Kobayashi O, Yoshida S, Yoshida A (2009) Genetic engineering of Candida utilis yeast for efficient production of L-lactic acid. Biosci Biotechnol Biochem 73:1818–1824
Ilmén M, Koivuranta K, Ruohonen L, Suominen P, Penttilä M (2007) Efficient production of l-lactic acid from xylose by Pichia stipitis. Appl Environ Microbiol 73:117–123
Ishida N, Suzuki T, Tokuhiro K, Nagamori E, Onishi T, Saitoh S, Kitamoto K, Takahashi H (2006a) D-lactic acid production by metabolically engineered Saccharomyces cerevisiae. J Biosci Bioeng 101:172–177
Ishida N, Saitoh S, Onishi T, Tokuhiro K, Nagamore E, Kitamoto K, Takahashi H (2006b) The effect of pyruvate decarboxylase gene knockout in Saccharomyces cerevisiae on L-lactic acid production. Biosci Biotechnol Biochem 70:1148–1153
John RP, Nampoothiri KM (2008) Strain improvement of Lactobacillus delbrueckii using nitrous acid mutation for L-lactic acid production. World J Microbiol Biotechnol 24:3105–3109
John RP, Anisha GS, Nampoothiri KM, Pandey A (2009) Direct lactic acid fermentation: focus on simultaneous saccharification and lactic acid production. Biotechnol Adv 27:145–152
Joshi DS, Singhvi MS, Khire JM, Gokhale DV (2010) Strain improvement of Lactobacillus lactis for D-lactic acid production. Biotechnol Lett 32:517–520
Kato H, Shiwa Y, Oshima K, Machii M, Araya-Kojima T, Zendo Y, Shimizu-Kadota M, Hattori M, Sonomoto K, Yoshikawa H (2012) Complete genome sequence of Lactococcus lactis IO-1, a lactic acid bacterium that utilizes xylose and produces high levels of L-lactic acid. J Bacteriol 194:2102–2103
Kharas GB, Sanchez-Riera F, Severson DK (1994) Polymers of lactic acid. In: Mobley DP (ed) Plastics from microbes: microbial synthesis of polymers and polymer precursors. Hanser Publishers, Munich, pp 93–137
Levering J, Musters MWJM, Bekker M, Bellomo D, Fiedler T, de Vos WM, Hugenholtz J, Kreikemeyer B, Kummer U, Teusing B (2012) Role of phosphate in the central metabolism of two lactic acid bacteria—a comparative systems biology approach. FEBS J 279:1274–1290
Liu Y, Gao W, Zhao X, Wang J, Garza E, Manow R, Zhou S (2014) Pilot scale demonstration of D-lactic acid fermentation facilitated by Ca(OH)2 using a metabolically engineered Escherichia coli. Biores Technol 169:559–565
Lunt J (1998) Large-scale production, properties and commercial applications of polylactic acid polymers. Polym Degrad Stabil 59:145–152
Maas RHW, Springer J, Eggink G, Weusthuis RA (2008) Xylose metabolism in the fungus Rhizopus oryzae: effect of growth and respiration on L(+)-lactic acid production. J Ind Microbiol Biotechnol 35:569–578
Marques S, Santos JAL, Girio FM, Roseiro JC (2008) Lactic acid production from recycled paper sludge by simultaneous saccharification and fermentation. Biochem Eng J 41:210–216
Mazumdar S, Clomburg JM, Gonzalez R (2010) Escherichia coli strains engineered for homofermentative production of d-lactic acid from glycerol. Appl Environ Microbiol 76:4327–4336
Mazumdar S, Blankschien M, Clomburg JM, Gonzalez R (2013) Efficient synthesis of L-lactic acid from glycerol by metabolically engineered Escherichia coli. Microb Cell Fact 12:7
Michelson T, Kask K, Jõgi E, Talpsep E, Suitso I, Nurk A (2006) L(+)-Lactic acid producer Bacillus coagulans SIM-7 DSM 14043 and its comparison with Lactobacillus delbrueckii ssp. lactis DSM 20073. Enzyme Microb Technol 39:861–867
Miller M, Suominen P, Aristidou A, Hause BM, van Hoek P, Dundon, CA (2012) Lactic acid-producing yeast cells having nonfunctional L- or D-lactate:ferricytochrome C oxidoreducatease cells. US Patent 8,137,953, 20 Mar 2012
Mimitsuda T, Sawai K, Kobayashi K, Tsukada T, Takeuchi N, Yamada K, Ogino H, Yonehara T (2014) Production of D-lactic acid in a continuous membrane integrated fermentation reactor by genetically modified Saccharomyces cerevisiae: Enhancement in D-lactic acid carbon yield. J Biosci Bioeng (in press)
Ohara H, Yahata M (1996) L-Lactic acid production by Bacillus sp. in anaerobic and aerobic culture. J Ferment Bioeng 81:272–274
Okano K, Yoshida S, Tanaka T, Ogino C, Fukuda H, Kondo A (2009a) Homo-D-lactic acid fermentation from arabinose by redirection of the phosphoketolase pathway to the pentose phosphate pathway in L-lactate dehydrogenase gene-deficient Lactobacillus plantarum. Appl Environ Microbiol 75:5175–5178
Okano K, Yoshida S, Yamada R, Tanaka T, Ogino C, Fukuda H, Kondo A (2009b) Improved production of homo-D-lactic acid via xylose fermentation by introduction of xylose assimilation genes and redirection of the phosphoketolase pathway to the pentose phosphate pathway in L-lactate dehydrogenase gene-deficient Lactobacillus plantarum. Appl Environ Microbiol 75:7858–7861
Okano K, Tanaka T, Ogino C, Fukuda H, Kondo A (2010) Biotechnological production of enantiomeric pure lactic acid from renewable resources: recent achievements, perspectives, and limits. Appl Microbiol Biotechnol 85:413–423
Okino S, Suda M, Fujijura K, Inui M, Yukawa H (2008) Production of D-lactic acid by Corynebacterium glutamicum under oxygen deprivation. Appl Microbiol Biotechnol 78:449–454
Osawa F, Fujii T, Nishida T, Tada N, Ohnishi T, Komeda T, Yoshida S (2009) Efficient production of L-lactic acid by Crabtree-negative yeast Candida boidinii. Yeast 26:285–296
Otto R (2012) Method for the production of lactic acid or a salt thereof by simultaneous saccharification and fermentation of starch. US Patent 8,119,376, 21 Feb 2012
Ou MS, Ingram LO, Shanmugam KT (2011) L(+)-lactic acid production from non-food carbohydrates by thermotolerant Bacillus coagulans. J Ind Microbiol Biotechnol 38:599–605
Ouyang J, Cai C, Chen H, Jiang T, Zheng Z (2012) Efficient non-sterilized fermentation of biomass-derived xylose to lactic acid by a thermotolerant Bacillus coagulans NL01. Appl Biochem Biotechnol 168:2387–2397
Pacheco A, Talaia G, Sá-Pessoa J, Bessa D, Gonçalves MJ, Moreira R, Paiva S, Casal M, Queirós O (2012) Lactic acid production in Saccharomyces cerevisiae is modulated by expression of the monocarboxylate transporters Jen1 and Ady2. FEMS Yeast Res 12:375–381
Paiva S, Devaux F, Barbosa S, Jacq C, Casal M (2004) Ady2p is essential for the acetate permease activity in the yeast Saccharomyces cerevisiae. Yeast 21:201–210
Patel M, Ou M, Ingram LO, Shanmugam KT (2004) Fermentation of sugar cane bagasse hemicellulose hydrolysate to L(+)-lactic acid by a thermotolerant acidophilic Bacillus sp. Biotechnol Lett 26:865–868
Patel MA, Ou MS, Harbrucker R, Aldrich HC, Buszko ML, Ingram LO, Shanmugam KT (2006) Isolation and characterization of acid-tolerant, thermophilic bacteria for effective fermentation of biomass-derived sugars to lactic acid. Appl Environ Microbiol 72:3228–3235
Payot T, Chemaly Z, Fick M (1999) Lactic acid production by Bacillus coagulans—kinetic studies and optimization of culture medium for batch and continuous fermentations. Enz Microb Technol 24:191–199
Porro D, Brambilla L, Ranzi BM, Martegani E, Alberghina L (1995) Development of metabolically engineered Saccharomyces cerevisiae cells for the production of lactic acid. Biotechnol Prog 11:294–298
Porro D, Bianchi M, Ranzi BM, Frontali L, Vai M, Winkler AA, Alberghina L (2006) Processes for producing lactic acid using yeast transformed with a gene encoding lactate dehydrogenase. US Patent 7,049,108, 23 May 2006
Posada JA, Cardona CA, Gonzalez R (2012) Analysis of the production process of optically pure D-lactic acid from raw glycerol using engineered Escherichia coli strains. Appl Biochem Biotechnol 166:680–699
Prior BA, Kilian SG, du Preez JC (1989) Fermentation of D-xylose by the yeasts Candida shehatae and Pichia stipitis: prospects and Problems. Proc Biochem 24:21–32
Pyle DJ, Garcia RA, Wen Z (2008) Producing docosahexaenoic acid (DHA)-rich algae from biodiesel-derived crude glycerol: effects of impurities on DHA production and algal biomass composition. J Agric Food Chem 56:3933–3939
Qin J, Zhao B, Wang X, Wang L, Yu B, Ma Y, Ma C, Tang H, Sun J, Xu P (2009) Non-sterilizes fermentative production of polymer-grade L-lactic acid by a newly isolated thermophilic strain Bacillus sp. 2–6. PLoS ONE 4:e4359
Qin J, Wang X, Zheng Z, Ma C, Tang H, Xu P (2010) Production of L-lactic acid by a thermophilic Bacillus mutant using sodium hydroxide as neutralizing agent. Biores Technol 101:7570–7576
Rallu F, Gruss A, Ehlich SD, Maguin E (2000) Acid- and multistress-resistant mutants of Lactococcus lactis: identification of intracellular stress signals. Mol Microbiol 35:517–528
Rico J, Yebra MJ, Pérez-Martínez G, Deutscher J, Monedero V (2008) Analysis of ldh genes in Lactobacillus casei BL23: role on lactic acid production. J Ind Microbiol Biotechnol 35:579–586
Rosenberg M, Rebroš M, Krištofíková L, Malátová K (2005) High temperature lactic acid production by Bacillus coagulans immobilized in LentiKats. Biotechnol Lett 27:1943–1947
Rossi DM, de Souze EA, Ayub MAZ (2013) Biodiesel residual glycerol metabolism by Klebsiella pneumoniae: pool of metabolites under anaerobiosis and oxygen limitation as a function of feeding rates. Appl Biochem Biotechnol 169:1952–1964
Sangproo M, Polyiam P, Jantama SS, Kanchanatawee S, Jantama K (2012) Metabolic engineering of Klebsiella oxytoca M5a1 to produce optically pure D-lactate in mineral salts medium. Biores Technol 119:191–198
Sawaii H, Sawai K, Sonoki T, Hatahira S (2011) Yeast and method of production L-lactic acid. US Patent 8,071,357, 6 Dec 2011
Shimizu-Kadota M, Kato H, Shiwa Y, Oshima K, Machii M, Araya-Kojima T, Zendo T, Hattori M, Sonomoto K, Yoshikawa H (2013) Genomic features of Lactococcus lactis IO-1, a lactic acid bacterium that utilizes xylose and produces high levels of L-lactic acid. Biosci Biotechnol Biochem 77:1804–1808
Shinkawa S, Okano K, Yoshida S, Tanaka T, Ogino C, Fukuda H, Kondo A (2011) Improved homo L-lactic acid fermentation from xylose by abolishment of the phosphoketolase pathway and enhancement of the pentose phosphate pathway in genetically modified xylose-assimilating Lactococcus lactis. Appl Microbiol Biotechnol 91:1537–1544
Singhvi M, Joshi D, Varma A, Gokhale D (2010) D-(-)-Lactic acid production from cellobiose and cellulose by Lactobacillus lactis mutant RM2-24. Green Chem 12:1106–1109
Song Z, Sun Y, Wei B, Xiu Z (2013) Two-step salting-out extraction of 1,3-propanediol and lactic acid from the fermentation broth of Klebsiella pneumoniae on biodiesel-derived crude glycerol. Eng Life Sci 13:487–495
Sumiya M, Davis EO, Packman LC, McDonald TP, Henderson PJ (1995) Molecular genetics of a receptor protein for D-xylose, encoded by the gene xylF, in Escherichia coli. Recept Chann 3:117–128
Suominen P, Aristidou A, Pentilla M, Ilmen M, Ruohonen L, Koivuranta K, Roberg-Perez K (2012) Genetically modified yeast of the species Issatchenkia orientalis and closely relates species, and fermentation processes using same. US Patent 8,097,448, 17 Jan 2012
Suzuki T, Sakamoto T, Sugiyama M, Ishida N, Kambe H, Obata S, Kaneko Y, Takahashi H, Harashima S (2013) Disruption of multiple genes whose deletion causes lactic acid resistance improves lactic acid resistance and productivity in Saccharomyces cerevisiae. J Biosci Bioeng 115:467–474
Tamakawa H, Ikushima S, Yoshida S (2012) Efficient production of L-lactic acid from xylose by a recombinant Candida utilis strain. J Biosci Bioeng 113:73–75
Tanaka K, Komiyama A, Sonomoto D, Ishizaki A, Hall SJ, Stanbury PF (2002) Two different pathways for D-xylose metabolism and the effect of xylose concentration on the yield coefficient of L-lactate in mixed-acid fermentation by the lactic acid bacterium Lactococcus lactis IO-1. Appl Microbiol Biotechnol 60:160–167
Tanaka T, Hoshina M, Tanabe S, Sakai K, Ohtsubo S, Taniguchi M (2006) Production of D-lactic acid from defatted rice bran by simultaneous saccharification and fermentation. Biores Technol 97:211–217
Tashiro Y, Kanedo W, Sun Y, Shibata K, Inokuma K, Zendo T, Sonomoto K (2011) Continuous D-lactic acid production by a novel thermotolerant Lactobacillus delbrueckii subsp. lactis QU 41. Appl Microbiol Biotechnol 89:1741–1750
Tian K, Chen X, Shen W, Prior BA, Shi G, Singh S, Wang Z (2012) High-efficiency conversion of glycerol to D-lactic acid with metabolically engineered Escherichia coli Afri. J Biotechnol 11:4860–4867
Tsuji H (2002) Autocatalytic hydrolysis of amorphous-made polylactides: effects of L-lactide content, tacticity, and enantiomeric polymer blending. Polymer 43:1789–1796
Tsuji H, Fukui I (2003) Enhanced thermal stability of poly(lactide)s in the melt by enantiomeric polymer blending. Polymer 44:2891–2896
Walton SL, Bischoff KM, van Heiningen ARP, van Walsum GP (2010) Production of lactic acid from hemicellulose extracts by Bacillus coagulans MXL-9. J Ind Microbiol Biotechnol 37:823–830
Wang Y, Li Y, Pei X, Yu L, Feng Y (2007) Genome-shuffling improved acid tolerance and L-lactic acid volumetric productivity in Lactobacillus rhamnosus. J Biotechnol 129:510–515
Wang P, Li J, Wang L, Tang ML, Yu ZL, Zheng ZM (2009) L(+)-Lactic acid production by co-fermentation of glucose and xylose with Rhizopus oryzae obtained by low-energy ion beam irradiation. J Ind Microbiol Biotechnol 36:1363–1368
Wang L, Zhao B, Liu B, Yang C, Yu B, Li Q, Ma C, Xu P, Ma Y (2010a) Efficient production of L-lactic acid from cassava powder by Lactobacillus rhamnosus. Biores Technol 101:7895–7901
Wang L, Zhao B, Liu B, Yu B, Ma C, Su F, Hua D, Li Q, Ma Y, Xu P (2010b) Efficient production of L-lactic acid from corncob molasses, a waste by-product in xylitol production, by a newly isolated xylose utilizing Bacillus strain. Biores Technol 101:7908–7915
Wang Q, Ingram LO, Shanmugam KT (2011) Evolution of D-lactate dehydrogenase activity from glycerol dehydrogenase and its utility for D-lactate production from lignocellulose. Proc. Nat. Acad Sci USA 108:18920–18925
Wang Y, Tian T, Zhao J, Wang J, Yan T, Xu L, Liu Z, Garza E, Iverson A, Manow R, Finan C, Zhou S (2012) Homofermentative production of D-lactic acid from sucrose by a metabolically engineered Escherichia coli. Biotechnol Lett 34:2069–2075
Wang Y, Li K, Huang F, Wang J, Zhao J, Zhao X, Garza E, Manow R, Grayburn S, Zhou S (2013) Engineering and adaptive evolution of Escherichia coli W for L-lactic acid fermentation from molasses and corn steep liquor without additional nutrients. Biores Technol 148:394–400
Wehrenberg RH (1981) Lactic-acid polymers—strong, degradable thermoplastics—research at Battelle proves the value of limited-lifetime plastics made from renewable resources. Mater Eng 94:63–66
Wu C, Zhang J, Chen W, Wang M, Du G, Chen J (2012) A combined physiological and proteomic approach to reveal lactic-acid-induced alterations in Lactobacillus casei Zhang and its mutant with enhanced lactic acid tolerance. Appl Microbiol Biotechnol 93:707–722
Wu X, Altman R, Eiteman MA, Altman E (2013a) Effect of overexpressing nhaA and nhaR on sodium tolerance and lactate production in Escherichia coli. J Biol Eng 7:3
Wu C, Zhang J, Du G, Chen J (2013b) Heterologous expression Lactobacillus casei RecO improved the multiple-stress tolerance and lactic acid production in Lactococcus lactis NZ9000 during salt stress. Biores Technol 143:238–241
Wu X, Altman R, Eiteman MA, Altman E (2014) Adaptation of Escherichia coli to elevated sodium concentrations increases cation tolerance and enables greater lactic acid production. Appl Environ Microbiol 80:2880–2888
Yáñez R, Moldes AB, Alonso JL, Parajó JC (2003) Production of D-lactic acid from cellulose by simultaneous saccharification and fermentation using Lactobacillus coryneformis subsp. torquens. Biotechnol Lett 25:1161–1164
Yáñez R, Alonso JL, Parajó JC (2005) D-lactic acid production from waste cardboard. J Chem Technol Biotechnol 80:76–84
Ye L, Zhao H, Li Z, Wu JC (2013a) Improved acid tolerance of Lactobacillus pentosus by error-prone whole genome amplification. Biores Technol 135:459–463
Ye L, Zhou X, Bin Hudari MS, Li Z, Wu JC (2013b) Highly efficient production of L-lactic acid from xylose by newly isolated Bacillus coagulans C106. Biores Technol 132:38–44
Yoshida S, Okano K, Tanaka T, Ogino C, Kondo A (2011) Homo-D-lactic acid production from mixed sugars using xylose-assimilating operon-integrated Lactobacillus plantarum. Appl Microbiol Biotechnol 92:67–76
Yu L, Pei X, Lei T, Wang Y, Feng Y (2008) Genome shuffling enhanced L-lactic acid production by improving glucose tolerance of Lactobacillus rhamnosus. J Biotechnol 134:154–159
Zhang ZY, Jin B, Kelly JM (2007) Production of lactic acid from renewable materials by Rhizopus fungi. Biochem Eng J 35:251–263
Zhao B, Wang L, Ma C, Yang C, Xu P, Ma Y (2010) Repeated open fermentative production of optically pure L-lactic acid using a thermophilic Bacillus sp. strain. Biores Technol 101:6496–6498
Zhao J, Xu L, Wang Y, Zhao X, Wang J, Garza E, Manow R, Zhou S (2013) Homofermentative production of optically pure L-lactic acid from xylose by genetically engineered Escherichia coli B. Microb Cell Fact 12:57
Zheng H, Gong J, Chen T, Chen X, Zhao X (2010) Strain improvement of Sporolactobacillus inulinus ATCC 15538 for acid tolerance and production of D-lactic acid by genome shuffling. Appl Microbiol Biotechnol 85:1541–1549
Zheng Z, Sheng B, Ma C, Zhang H, Gao C, Su F, Xu P (2012) Relative catalytic efficiency of ldhL- and ldhD-encoded products is crucial for optical purity of lactic acid produced by Lactobacillus strains. Appl Environ Microbiol 78:3480–3483
Zhou Y, Dominguez JM, Cao N, Du J, Tsao GT (1999) Optimization of L-lactic acid production from glucose by Rhizopus oryzae ATCC 52311. Appl Biochem Biotechnol 77–79:401–407
Zhou SD, Causey TB, Hasona A, Shanmugam KT, Ingram LO (2003) Production of optically pure D-lactic acid in mineral salts medium by metabolically engineered Escherichia coli W3110. Appl Environ Microbiol 69:399–407
Zhou SD, Shanmugam KT, Ingram LO (2004) Functional replacement of the Escherichia coli D-(-)lactate dehydrogenase gene (ldhA) with the L-(+)-lactate dehydrogenase gene (ldhL) from Pediococcus acidilactici. Appl Environ Microbiol 69:2237–2244
Zhu Y, Eiteman MA, Dewitt K, Altman E (2007) Homolactate fermentation by metabolically engineered Escherichia coli strains. Appl Environ Microbiol 73:456–464
About this article
Cite this article
Eiteman, M.A., Ramalingam, S. Microbial production of lactic acid. Biotechnol Lett 37, 955–972 (2015). https://doi.org/10.1007/s10529-015-1769-5