Growth parameters of Liberibacter crescens suggest ammonium and phosphate as essential molecules in the Liberibacter-plant host interface
Liberibacter crescens is the closest cultured relative of four important uncultured crop pathogens. Candidatus. L. asiaticus, L. americanus, L. africanus cause citrus greening disease, while Ca. L. solanacearum causes potato Zebra chip disease. None of the pathogens grows in axenic culture. L. crescens grows in three media: a BM-7, a serum-free Hi® Grace’s Insect Medium (Hi-GI), and a chemically-defined medium called M15. To date, no optimal growth parameters of the model species L. crescens have been reported. Studying the main growth parameters of L. crescens in axenic culture will give us insights into the lifestyle of the Ca. Liberibacter pathogens.
The evaluation of the growth parameters—pH, aeration, temperature, and buffering capacity—reflects the optimal living conditions of L. crescens. These variables revealed that L. crescens is an aerobic, neutrophilic bacterium, that grows optimally in broth in a pH range of 5.8 to 6.8, in a fully oxygenated environment (250 rpm), at 28 °C, and with monosodium phosphate (10 mM or 11.69 mM) as the preferred buffer for growth. The increase of pH in the external media likely results from the deamination activity within the cell, with the concomitant over-production of ammonium in the external medium.
L. crescens and the Ca. Liberibacter pathogens are metabolically similar and grow in similar environments—the phloem and the gut of their insect vectors. The evaluation of the growth parameters of L. crescens reveals the lifestyle of Liberibacter, elucidating ammonium and phosphate as essential molecules for colonization within the hosts. Ammonium is the main driver of pH modulation by active deamination of amino acids in the L. crescens amino acid rich media. In plants, excess ammonium induces ionic imbalances, oxidative stress, and pH disturbances across cell membranes, causing stunted root and shoot growth and chlorosis—the common symptoms of HLB-disease. Phosphate, which is also present in Ca. L. asiaticus hosts, is the preferred buffer for the growth of L. crescens. The interplay between ammonium, sucrose, potassium (K+), phosphate, nitrate (NO3−), light and other photosynthates might lead to develop better strategies for disease management.
KeywordsLiberibacter Lifestyle Growth parameters pH Aeration Temperature Buffering capacity Ammonium Phosphate Concentrations Pathogens Disease Management
Acid tolerance response
Fetal bovine serum
Hi Grace’s insect medium
Nicotinamide adenine dinucleotide
One factor at a time methodology
-log10 of the acid dissociation constant (Ka)
Proton motive force
Revolutions per minute
The genus Liberibacter comprises reduced-genome, fastidious α-proteobacteria including the not yet cultured Ca. Liberibacter species, which are responsible for the devastating citrus greening, or Huanglongbing (HLB), and potato zebra chip (ZC) diseases worldwide . Three species—Ca. L. asiaticus, Ca. L. americanus, and Ca. L. africanus—are the casual agents of HLB while Ca. L. solanacearum is responsible for potato ZC . In Florida, citrus production has been severely affected since the discovery the citrus greening disease in 2005 . The pathogenic Ca. Liberibacter species are transmitted into the phloem of citrus and potato plants by phloem feeders from the family psyllidae . The genus Liberibacter also includes the endophytic bacterium Ca. L. europaeus found in carrots and celery as well as the only culturable species, L. crescens, which was isolated from mountain papaya in 1995 [4, 5]. L. crescens might be a non-pathogenic species because several attempts to inoculate it into citrus, mountain papaya, dodder, and the Asian citus psyllid—Diaphorina citri, have all failed . Compared to Ca. Liberibacter pathogens, L. crescens contains a slightly larger genome, which most likely confers the metabolic capabilities to grow in vitro [7, 8]. Since L. crescens is the sole cultured member of the genus Liberibacter, it is the best and closest model bacteria to study the lifestyle and metabolism of Ca. Liberibacter pathogens.
Fast-growing model bacteria such as Escherichia coli and Bacillus subtilis grow in complex and chemically-defined media in which the optimal chemical and physical growth parameters have been determined . In the genus Liberibacter, the only species in which these conditions can be studied is L. crescens. Chemical factors such as carbon sources and essential nutrients were recently studied for L. crescens in the M15 chemically-defined medium . Here, citrate was proposed as the preferred carbon source for the growth of L. crescens at slightly acid conditions. Citrate is abundant in the citrus phloem and present in the psyllid haemolymph where Ca. L. asiaticus thrives [11, 12]. Physical factors such as pH, aeration, and temperature  have not been fully described for L. crescens in axenic culture, except for the optimal temperature for growth at 27–28 °C and an initial pH of 6.5 [4, 8].
Here, the optimal growth conditions of L. crescens are presented for four growth parameters—pH, aeration, temperature and buffering capacity—using one factor at a time methodology (OFAT) . The evaluation of the growth parameters of L. crescens gave insight into the physiology, lifestyle and culturability of the Ca. Liberibacter pathogens. The growth parameters indicated that L. crescens grows optimally in an initial pH of 5.8 to 6.8, in a fully oxygenated environment, at 28 °C, and monosodium phosphate as the most suitable buffer for growth. Similar to L. crescens, Ca. Liberibacter asiaticus might also require acidic conditions to grow because the citrus phloem is acidic (5.0–5.74) . Ca. Liberibacter species are also expected to be aerobic pathogens because they contain the complete TCA cycle and respiratory chain machinery . The optimal temperatures in which Ca. L. asiaticus grew in the citrus phloem is also at 22/27 °C night/day photoperiod . Phosphoric acid is also present in the citrus phloem (1.14–9.16 mM), which might be an indication of the phosphorus requirements for Ca. L. asiaticus growth .
The evaluation of the growth parameters of L. crescens also highlighted the mechanisms of pH modulation for Liberibacter growth. In gram-negative neutrophilic aerobic bacteria such as Liberibacter species the acid tolerance response (ATR) is activated when they are exposed to slightly acidic conditions. ATR mechanisms include the consumption of protons through decarboxylation of amino acids, the consumption of protons through the respiratory chain, and ammonia generation through active deamination of amino acids [16, 17]. Therefore, the increase of pH in relation to growth in L. crescens cultures most likely resulted from the accumulation of ammonium in milimolar concentrations in the external cell culture media. Similarly in the amino acid-rich phloem sap [11, 18], Ca. L. asiaticus might be deaminating amino acids with the concomitant over production of ammonium. Excess ammonium is toxic for plants, inducing ionic imbalances, oxidative stress, and disturbances of the pH gradients across plant membranes . These events lead to leaf chlorosis and inhibition of root and shoot growth, which are also some of the common symptoms of HLB-infected trees [19, 20].
Studying the factors that influence the growth of L. crescens will contribute to the understanding of the physiology and the lifestyle of the Ca. Liberibacter pathogens. The optimal living conditions, the discovery of phosphate as the preferred buffer for L. crescens growth, and the accumulation of ammonium in L. crescens cultures open new avenues to understand Ca. Liberibacter culturing and to develop nutritional strategies utilizing sucrose, phosphate, potassium, nitrate, and light to alleviate HLB-symptoms [21, 22, 23, 24, 25, 26].
Growth parameters of Liberibacter crescens in axenic culture
First step: evaluating the optimal pH for L. crescens growth
In M15 chemically-defined medium, L. crescens grew best at pH 5.92 compared to the other initial pH tested (Tukey HSD p < 0.001), with exception of pH 6.0 (Tukey HSD, p = 0.31) (Fig. 2; see Additional file 1) However, the growth is slightly better in M15 pH 5.92 compared to M15 pH 6.0 (Fig. 2; see Additional file 1). The optimal pH range in Hi-GI encompassed 5.8 to 6.2, where L. crescens grew similarly (Tukey HSD, 0.65 < p < 0.99); whereas in the other pH, the growth was significanlty reduced (Tukey HSD, p < 0.001) (Fig. 3; see Additional file 1). In BM-7, the optimal growth was between pH 5.8 and 6.8 (Tukey HSD, 0.99 < p < 1), followed by pH 6.9, 5.6, and 7.0 (Tukey HSD, 0.4 < p < 0.99) (Fig. 4; see Additional file 1). The growth of L. crescens in BM-7 with a pH lower than 5.6 was significantly reduced compared to the pH range between 5.6 and 7.0 (Tukey HSD, p < 0.001), requiring longer time to enter in exponential phase (Fig. 4; see Additional file 1). In BM-7 media with pH higher than 7.0, L. crescens grows poorly (Tukey HSD, p < 0.001) (Fig. 4; see Additional file 1). Strong positive spearman rho and pearson linear correlations were found between optical density and external pH in M15, Hi-GI, and BM-7 (see Additional file 2). Since L. crescens grew poorly in BM-7 media with a pH higher than 7.4, the correlations between pH and growth were also small. (Fig. 4, pH 7.6 to 8.2; see Additional file 1). An increase in pH alongside an increase in optical density was evident in all media (Figs. 2, 3, 4; see Additional file 1).
L. crescens grew optimally at an initial pH ranging from 5.8 to 6.8 in axenic culture. Ideal growth was achieved at pH 5.92 for M15 and Hi-GI media, whereas in BM-7, ideal growth was obtained at pH 6.5. In the media with a pH lower than 5.8, L. crescens grew poorly, requiring more time to start exponential growth. At this lower pH, L. crescens still induced a pH increase in the media, which might reflect the ability of the cells to survive and adapt to acidic conditions, even at low titers. The limitations to culture Ca. L. asiaticus might be reflected in the inability to keep higher titers within the acidic phloem sap [11, 27].
Second step: determining aeration levels for the growth of L. crescens
Third step: optimal temperature for growth of L. crescens
Fourth step: the buffering requirements for L. crescens growth
The fourth variable evaluated for L. crescens growth was the ability of buffers to prevent the pH increase of the medium over time, in hopes that this would improve culture growth. The buffers tested include MES (pKa = 6.2), Bis-Tris hydrochloride (pKa = 6.5), ACES (pKa = 6.8), and monosodium phosphate (pKa = 7.2) at 10, 25 and 50 mM concentrations. ACES buffer is present in the BM-7 at 54.3 mM, whereas monosodium phosphate buffer is present in the M15 at 11.69 mM and in Hi-GI medium at 8.4 mM.
The inability of the buffers to control the increase of pH suggests that L. crescens posses an endogenous mechanism to maintain pH homeostasis inside the cell. In the slightly acidic environment in which L. crescens grows, the influx of H+ protons to the cell might contribute to generate proton motive force (PMF) . However, excess proton uptake might also impair pH homeostasis in the cytoplasmic space . Therefore, excess of protons inside and outside the cell requires to be controlled by a pH regulatory mechanism , which can guarantee the proper growth of L. crescens in slightly acidic conditions.
Optimal phosphate levels for the growth of L. crescens
pH modulation in L. crescens cultures in the M15 chemically-defined medium
To further investigate the cause of the pH increase during growth of L. crescens cultures, three potential phenomena associated with pH homeostasis within the cell were studied in the M15 chemically-defined medium: citrate metabolism, ornithine metabolism, and ammonium accumulation in the external media.
Ammonium accumulation of L. crescens cultures
Spearman rank correlation and Pearson lineal correlation of L. crescens cultures in M15 medium. Correlations were established among the concentration of ammonia, the increase of pH and the growth (OD600) of L. crescens. The three variables are positively and highly correlated with correlation coefficients ranging from 0.88 to 0.96
Spearman Rho (R)
Cell viability in the optimal growth conditions of L. crescens
In order to provide more accurate information about the period required for the growth of L. crescens, the viability of the cells was monitored in the three optimized media using the Presto Blue viability reagent assay. The reducing ability of living cells causes rezasurin—the active ingredient of presto blue—to be reduced to resorufin, a highly fluorescent compound . Thus, the amount of fluorescence is proportional to the living cells present in the media. Maximal viability of the cells is achieved between 72 to 96 h for M15 and Hi-GI, and 48 to 72 h for BM-7 (Fig. 14; see Additional file 1). The fluorescence levels observed are representative of the growth curves, where Hi-GI medium has the highest peak viability level, followed by M15 and BM-7 media. A gradual cell death starts at 120 h in M15 and Hi-GI while an abrupt live-cell decline is found in BM-7 at 96 h (Fig. 14; see Additional file 1). Optical density is simultaneously monitored in the same cultures to correlate with cell viability over time (Fig. 14; see Additional file 1).
The evaluation of the growth parameters of L. crescens reveals the lifestyle of the Ca. Liberibacter pathogens. The evaluation strategy showed that L. crescens grows optimally in axenic culture at a pH between 5.8–6.8, at 28 °C, with phosphate as the preferred buffer for growth. The citrus phloem in which Ca. L. asiaticus resides has a pH of 5.0 to 5.74 . In this acidic pH, L. crescens struggles to grow, requiring more time to enter into the exponential phase. The low titers of Ca. L. asiaticus in the citrus phloem might be associated with the acidic conditions this pathogen faces prior to colonization . Thus, Liberibacter species appear to be neutrophilic bacteria that adapted to slightly acidic environments. Similar to L. crescens optimal growth temperature (27/28 °C), Ca. L. asiaticus and Ca. L. americanus have also reported optimal growth in the citrus phloem at 22/27 °C night/day photoperiod .
None of the buffers improved the growth of L. crescens compared to the controls. However, monosodium phosphate buffer at 10 mM promoted the growth of L. crescens at similar rates to those of the three media controls. Phosphate buffer is commonly used in the growth of neutrophilic bacteria, not only to maintain pH, but as a source of phosphorous. Phosphate is present in the phloem of different citrus cultivars at concentrations between 1.14 and 9.16 mM . It is also present in the haemolymph of D. citri at a concentration of 4.77 mM per psyllid haemolymph . Substantial growth of L. crescens was observed with phosphate buffer at concentrations between 5 mM and 11.69 mM in M15 medium. Optimal growth was observed at 10 mM and 11.69 mM. Higher concentrations than 11.69 mM phosphate should be carefully considered because phosphate and citrate together, in a medium rich in calcium, induce calcium phosphate precipitation, leading to erroneous results . Since HLB-affected plants have been reported to be deficient in phosphorous , it is likely that Ca. L. asiaticus also requires phosphorous in the form of phosphate to survive within the hosts. However, the phosphorous-deficient HLB-affected citrus plants might also require the spray of phosphate in concentrations lower than 3 mM to improve the health of the trees and to reduce Ca. L. asiaticus titers . Thus, phosphate might play an important role in reducing disease symptoms.
The increase of pH during culture growth, even using different buffers, can be explained by the accumulation of ammonium in milimolar concentrations in the external medium of L. crescens cultures. In Arabidopsis thaliana, the production of ammonium even at micromolar concentrations by several strains of rhizosphere bacteria induces plant growth inhibition and chlorosis [19, 37]. The citrus phloem and psyllid haemolymph are rich in amino acids with concentrations ranging from 0.16 to 44.9 mM per citrus phloem sample and 0.008 to 0.75 mM per psyllid haemolymph sample [11, 12]. In the rich amino acid phloem environment, Ca. L. asiaticus might also deaminate amino acids resulting in the accumulation of ammonium in the phloem. In the citrus plants, excess ammonium could further induce ionic and pH disturbances as well as oxidative stress. These events lead to leaf chlorosis and stunted roots and shoots, the common symptoms of HLB-disease [19, 20].
The deamination activity in L. crescens is not well understood. All Liberibacter species contain glutaminase, which deaminates glutamine to glutamate and ammonia . L. crescens and Ca. L. asiaticus have NAD-glutamate dehydrogenase, which converts L-glutamate to α-ketoglutarate and ammonia . However, preliminary studies show that none of these enzymes is responsible for ammonium release and the pH increase in the external media of L. crescens (data not shown). Other worth-considering alternative is the presence of two nucleoside deaminases in L. crescens and Ca. L. asiaticus, which catalyze the hydrolytic deamination of cytidine and adenosine to uridine and inosine with the concomitant production of ammonia . However, the activity of these nucleoside deaminases is not expected to generate the high concentrations of ammonium found in L. crescens culture media. Improvements in the functional annotation of Liberibacter genomes could lead to better identify ammonia-producing enzymes in these bacteria.
Since excess ammonium is toxic for the plants, its uptake and assimilation has to be tightly regulated through saturable high affinity (ammonium transporters AMTs) and non-saturable low affinity uptake systems (aquaporins or cation channels) . In citrus plants, ammonium uptake in the roots is regulated by light and sucrose availability in the roots. Illumination in the shoots stimulates photosynthesis with the concomitant production of soluble photosynthates such as sucrose, glucose, fructose and organic acids . These photosynthates, especially sucrose, are transported via phloem to the roots, to facilitate the high affinity uptake of ammonium through the CitAMT1 transporter. Sucrose acts as signal molecule that coordinates between N uptake systems and C activity in the roots . Carbon availability and reducing equivalents are necessary to induce ammonium uptake and assimilation in the roots . In plants with limited C root assimilatory capabilities, ammonium is loaded into the xylem and subsequently assimilated into sink compartments such as mesophyll cells and companion cells [42, 43]. The phloem is the main transport system of sugars, carboxylic acids and amino acids from source to sink growing tissues in the shoots and in the roots . Ammonium can be assimilated in the phloem companion cells using the glutamine synthetase/glutamate synthase (GS/GOGAT) system or the glutamate dehydrogenase (GDH) [44, 45]. However, ammonium is not loaded into the phloem , for which over-accumulation of ammonium in the phloem sieve tubes by pathogen activity could lead to nitrogen (N) imbalances with toxic effects to the citrus plants.
Strategies to regulate the accumulation of ammonium in the phloem are not well studied yet. However, several ways to lower excess ammonium in the plant as a whole have been reported. For instance, increasing the light intensity to wheat plants and citrus plants can induce a higher ammonium accumulation rate to amino acids and proteins in the roots due to higher tricarboxylic acid loading and the activation of GDH [21, 25]. The application of exogenous carbon supplies such as sucrose in to citrus and calcium carbonate (CaCO3) to cucumber provides with additional carbon (C) skeletons for NH4+ assimilation in the roots [21, 22]. The addition of increased concentrations of K+ reduces ammonium flux to the roots by active competition for transport through K+ specific channels in rice . Low doses of nitrate can also contribute to reduce ammonium toxicity since NO3− uptake induces alkalization of the medium to counterbalance the effect of NH4+ [24, 26]. Finally, the addition of phosphate to the roots of A. thaliana induces ammonium phosphate salt precipitates restoring plant growth . If Ca. L. asiaticus growth contributes to the accumulation of ammonium in the citrus phloem, the interplay between ammonium and these ions and molecules could contribute to alleviate HLB-symptoms. However, these strategies need to be studied in more detail. The molecular mechanisms of deamination in Liberibacter species, the accumulation of ammonium in the citrus phloem, the potential effects of the different strategies to reduce the ammonium levels in the phloem of citrus plants as well as more thorough statistical methods to evaluate growth optimization parameters (E.g. Surface Response Methodology and Placket-Burman Plot) are still subjects of investigation.
The evaluation strategy for the growth of L. crescens opens new avenues to understand the lifestyle of Liberibacter species and the potential interactions within the hosts. L. crescens grows in slightly acidic conditions, at 28 °C, in a fully oxygen environment and phosphate as the preferred buffer for growth. Ca. Liberibacter pathogens are expected to grow in similar environmental conditions to those of L. crescens because they are metabolically similar and grow in similar environments—the phloem sap and their insect vectors. In Ca. L. asiaticus, different factors such as the slightly acidic citrus phloem, the repertory of enzymes for aerobic respiration, the optimal growth temperatures within the phloem, and the phosphoric acid present in the hosts highlight these similarities. The accumulation of ammonium is the main driver of pH modulation in Liberibacter species. In citrus plants, excess ammonium is expected to induce ionic stress, pH imbalances, and disturbances to the host cell membranes, with the concomitant development of HLB-disease symptoms. Studying different strategies to reduce ammonium in the citrus phloem might lead to reduce symptoms in HLB-affected trees.
Reagents, bacterial strains, and culture conditions
TNM-FH insect medium and Fetal Bovine Serum (FBS) were purchased through Gemini Bio-products (Sacramento, CA). Hi Grace’s Insect Medium (Hi-GI) was purchased through Hi-Media (Mumbai, India). Citric acid was purchased through Fisher Scientific (Pittsburgh, PA), L-arginine hydrochloride through Calbiochem (San Diego, CA), L-lysine monohydrochloride through Acros-organics (Geel, Belgium), and methionine sulfoxide through Alfa Aesar (Haverhill, MA). All other reagents were obtained through Sigma-Aldrich (St. Louis, MO), unless specified. BM-7 and M15 media were prepared as described previously [8, 10]. For M15 preparation, most components were dissolved with gentle stirring, except for L-tyrosine and three non-water soluble vitamins—biotin, folic acid and riboflavin. L-tyrosine was dissolved in 15 ml of 2 mM HCl prior to addition to M15. Biotin was dissolved in dimethyl sulfoxide, folic acid in 0.1 M NaOH, and riboflavin in 0.01 M NaOH. DL-serine of M15 was replaced by L-serine. Hi-Gi medium was prepared according to the manufacturer instructions. Briefly, 45.9 g of Hi-GI were dissolved in 950 mL of sterile, deionized water, slowly adjusting the pH to 5.92 by titration with 5 M KOH. After completing to 1 L, Hi-GI was sterilized through a 0.22 μm sterile filter. L. crescens strain BT-1 was used in all experiments.
Growth parameters assays for L. crescens cultures
Four variables were considered to study growth parameters of L. crescens including pH, aeration, temperature, and buffering capacity. These variables were evaluated using one-factor-at-a-time (OFAT) methodology  in the three growth media of L. crescens (Fig. 1). pH optimization was the first parameter to be evaluated using an initial pH of 5.0 with increasing 0.2 values until salt precipitation occurs in the media. pH of all media and buffers was equilibrated at room temperature (24–25 °C). With the optimal growth pH, three different levels of aeration were further evaluated: 150, 200, and 250 rpm. Subsequently, optimal temperature for L. crescens growth was assessed at 22, 28 and 32 °C. Finally, four different buffers—monosodium phosphate, ACES, BIS-TRIS, and MES—with dissociation constants (pKa) close to the optimal growth pH of L. crescens were also evaluated at 10, 25, and 50 mM concentrations (Fig. 1).
Liberibacter crescens inoculum source
pH modulation assays in L. crescens cultures
Three potential causes for the pH modulation in L. crescens cultures were evaluated in M15 chemically-defined medium: citrate metabolism, ornithine metabolism, and ammonium accumulation in the cell-free supernatant.
L. crescens was grown in Hi-GI broth to exponential phase (OD600~0.7–0.8, Fig. 16; see Additional file 1), and washed with the previously described sterile ACES-KOH buffer pH 6.5 prior to inoculation in 30 mL of M15 and M15 without citrate. Optical density and pH were monitored as described previously once a day for 13 days.
L. crescens was grown in Hi-GI broth to exponential phase (OD600~0.7–0.8, Fig. 16; see Additional file 1), and washed with the previously described sterile ACES-KOH buffer pH 6.5 prior to inoculation in 30 mL of M15 and M15 without ornithine. Optical density and pH were monitored as described previously once a day for 13 days.
Determination of ammonium in M15 cell-free supernatant
L. crescens was grown in Hi-GI broth to exponential phase (OD600~0.7–0.8, Fig. 16; see Additional file 1), and washed with the previously described sterile ACES-KOH buffer pH 6.5 prior to inoculation in 30 mL of M15 media in triplicate. Optical density and pH were monitored once a day for a 13-day period. 50 μL of cell-free supernatant was also collected every day and stored at − 80 °C for subsequent ammonium analysis. Ammonium quantification over time was monitored using an ammonia/ammonium assay kit (Bioassay systems, Hayward, CA) following manufacturer recommendations. Briefly, cell-free supernatant samples and M15 negative control samples were diluted to 10-fold in ultrapure water. Standards were also prepared in 10-fold diluted M15 control in ultrapure water. The enzyme reaction contained 180 μL of assay buffer, 1 μL of enzyme, 8 μL of reconstituted NADH reagent, and 1 μL of ketoglutarate per sample. The blank control reaction contained the same components, except for the enzyme. Control and the experimental samples (20 μL) were mixed each with 180 μL of enzyme reaction and 180 μL of blank control reaction respectively in a 96 well plate. The plate was incubated for 30 min at room temperature. Absorbance was monitored at 340 nm using the Synergy BioTek Multi-mode microplate reader (BioTek Instruments, Inc). Ammonium concentrations were calculated accordingly using the manufacturer recommendations.
Cell viability assay for L. crescens in optimal growth media conditions
Cell viability of L. crescens in the best optimal conditions was monitored using Presto Blue cell viability reagent (Invitrogen). L. crescens was first cultivated in Hi-GI broth to exponential phase (OD600~0.7–0.8, Fig. 16; see Additional file 1), and subsequently washed with the previously described sterile ACES-KOH buffer pH 6.5 prior to inoculation in 30 mL of M15, Hi-GI, or BM-7 media. 25 μL of Presto Blue were mixed with 225 μL of L. crescens culture samples in a black 96-well plate and incubated for two hours in the dark. Fluorescence was measured at 530/25 and 615/16 (excitation/emission) range with a gain of 45 using the Synergy BioTek Multi-mode microplate reader (BioTek Instruments, Inc). Cell viability was monitored once a day for 13 days along with optical density (OD600) of the cell cultures. Experiments were done by triplicate.
Analysis of variance was used to determine relationships between the different media at any given condition. Post-hoc TukeyHSD test was subsequently used to determine statically significant traits in cell growth and pH among the media. Spearman rank (Rho) and Pearson linear correlations were used to correlate growth (OD600), pH, and ammonium concentrations over time. All tests were performed using R programming software version 3.3.2.
The authors thank Dr. Willard H. Harrison from the Department of Chemistry and Vincent Wing from the writing studio of the University of Florida for their valuable comments while writing the manuscript.
MC-M and EWT conceived the research. MC-M and EWT wrote the paper. JRP and MAR helped editing the paper. AM-B and JRP helped M-CM with the experiments. MAR contributed with the statistical analyses. All authors read and approved the final version of this manuscript.
Citrus Research and Development Foundation through Project No. 016–009, the University of Florida’s Institute of Food and Agricultural Sciences, and the Fulbright-Colciencias Scholarship of the Colombian Government. The funding bodies played no role in study design, collection, analysis, interpretation or data, or writing the manuscript.
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The authors declare that they have no competing interests.
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