Abstract
A large variety of prokaryotes are capable of accumulating polyhydroxyalkanoates (PHAs) as water-insoluble inclusions in the cytoplasm, and are referred to as PHA granules. Generally, PHAs represent storage compounds for carbon and energy, and they are synthesized under unbalanced growth conditions, i.e., when the carbon source is available in excess and when another nutrient is limited at the same time. In this case, further microbial growth is prevented, and PHAs are accumulated in the cytoplasm of the cells. These PHAs may possess molecular masses of up to several million daltons, and the polyester might represent the major cell constituent, contributing up to 90% or even more of the cellular dry weight. At the beginning of this chapter a brief overview about the PHA synthase and the different metabolic pathways occurring in prokaryotes will be given. The main topic focuses on the biogenesis of PHA granules and the chemical and physical properties of PHA granules produced by bacteria. The function of granule-associated proteins during the biogenesis and mobilization of PHA granules will also be discussed in detail. The chapter will be completed with an overview about applications of PHA granules as surface coatings and as nanoparticles.
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References
Abe T, Kobayashi T, Saito T (2005) Properties of a novel intracellular poly(3-hydroxybutyrate) depolymerase with high specific activity (PhaZd) in Wautersia eutropha H16. J Bacteriol 187:6982–6990
Anderson AJ, Dawes EA (1990) Occurrence, metabolism, metabolic role, and industrial uses of bacterial polyhydroxyalkanoates. Microbiol Rev 54:450–472
Asrar J, Gruys KJ (2002) Biodegradable polymer (Biopol®) In: Doi Y, Steinbüchel A (eds) Biopolymers, vol 4. Polyesters III—applications and commercial products. Wiley, Weinheim, pp 53–90
Banki MR, Gerngross TU, Wood DW (2005) Novel and economical purification of recombinant proteins: intein-mediated protein purification using in vivo polyhydroxybutyrate (PHB) matrix association. Protein Sci 14:1387–1395
Boatman ES (1964) Observations on the fine structure of spheroplasts of Rhodospirillum rubrum. J Cell Biol 20:297–311
Bohmert K, Balbo I, Steinbüchel A, Tischendorf G, Willmitzer L (2002) Constitutive expression of the β-ketothiolase gene in transgenic plants. A major obstacle for obtaining polyhydroxybutyrate-producing plants. Plant Physiol 128:1282–1290
Cox MK (1992) In: Vert M, Feijen J, Albertsson A, Scott G, Chiellini E (eds) Biodegradable polymers and plastics. Royal Society of Chemistry, Cambridge, p 95
De Koning GJM, Maxwell IA (1993) Biosynthesis of poly-(R)-3-hydroxyalkanoate: an emulsion polymerization. J Environ Polym Degrad 1:223–226
Dennis D, Liebig C, Holley T, Thomas KS, Khosla A, Wilson D, Augustine B (2003) Preliminary analysis of polyhydroxyalkanoate inclusions using atomic force microscopy. FEMS Microbiol Lett 226:113–119
De Smet MJ, Eggink G, Witholt B, Kingma J, Wynberg H (1983) Characterization of intracellular inclusions formed by Pseudomonas oleovorans during growth on octane. J Bacteriol 154:870–878
Doi Y, Abe C (1990) Biosynthesis and characterization of a new bacterial copolyester of hydroxyalkanoates and 3-hydroxy-ω-chloroalkanoates. Macromolecules 23:3705–3707
Doi Y, Tamaki A, Kunioka M, Soga K (1987) Biosynthesis of terpolyesters of 3-hydroxybutyrate, 3-hydroxyvalerate and 5-hydroxyvalerate from chlorpentanoic and pentanoic acids. Makromol Chem Rapid Commun 8:631–635
Doi Y, Segawa A, Nakamura S, Kunioka MT (1990) Production of biodegradable copolyesters by Alcaligenes eutrophus. In: Dawes EA (ed) New biosynthetic biodegradable polymers of industrial interest from microorganisms. Kluwer, Dordrecht, pp 37–48
Fischer H, Erdmann S, Holler E (1989) An unusual polyanion from Physarium polycephalum that inhibits homologous DNA polymerase alpha in vitro. Biochemistry 28:5219–5226
Fukui T, Doi A (1997) Cloning and analysis of the poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) biosynthesis genes of Aeromonas caviae. J Bacteriol 179:4821–4830
Fuller RC, O’Donnel JP, Saulnier J, Redlinger TE, Foster J, Lenz JW (1992) The supramolecular architecture of the polyhydroxyalkanoate inclusions in Pseudomonas oleovorans. FEMS Microbiol Rev 103:279–288
Gerngross TU, Reilly P, Stubbe J, Sinskey AJ, Peoples OP (1993) Immunocytochemical analysis of poly-β-hydroxybutyrate (PHB) synthase in Alcaligenes eutrophus H16: localization of the synthase enzyme at the surface of the of PHB granules. J Bacteriol 175:5289–5293
Gottschalk G (1964a) Die Biosynthese der Poly-β-Hydroxybuttersäure durch Knallgasbakterien. I. Ermittlung der 14C-Verteilung in Poly-β-Hydroxybuttersäure. Arch Mikrobiol 47:225–229
Gottschalk G (1964b) Die Biosynthese der Poly-β-Hydroxybuttersäure durch Knallgasbakterien. II. Verwertung organischer Säuren. Arch Mikrobiol 47:230–235
Griebel RJ, Merrick JM (1971) Metabolism of poly-β-hydroxybutyrate: effect of mild alkaline extraction on native poly-β-hydroxybutyrate granules. J Bacteriol 108:782–789
Griebel RJ, Smith Z, Merrick JM (1968) Metabolism of poly-β-hydroxybutyrate granules from Bacillus megaterium. Biochemistry 7:3676–3681
Handrick R, Technow U, Reichart T, Reinhardt S, Sander T, Jendrossek D (2004a) The activator of the Rhodospirillum rubrum PHB depolymerase is a polypeptide that is extremely resistant to high temperature (121 °C) and other physical or chemical stresses. FEMS Microbiol Lett 230:265–274
Handrick R, Reinhardt S, Schultheiss D, Reichart T, Schüler D, Jendrossek V, Jendrossek D (2004b) Unraveling the function of the Rhodospirillum rubrum activator of polyhydroxybutyrate (PHB) degradation: the activator is a PHB-granule-bound protein (phasin). J Bacteriol 186:2466–2475
Haywood GW, Anderson AJ, Chu L, Dawes AE (1988a) Characterization of two 3-ketothiolases possesing differing substrate specificities in the polyhydroxyalkanoate synthesizing organism Alcaligenes eutrophus. FEMS Microbiol Lett 52:91–96
Haywood GW, Anderson AJ, Chu L, Dawes AE (1988b) The role of NADH-and NADPH-linked acetoacetyl-CoA reductases in the poly-3-hydroxybutyrate synthesizing organism Alcaligenes eutrophus. FEMS Microbiol Lett 52:259–264
Haywood GW, Anderson AJ, Dawes AE (1989) The importance of PHB-synthase substrate specificity in polyhydroxyalkanoate synthesis by Alcaligenes eutrophus. FEMS Microbiol Lett 57:1–6
Haywood GW, Anderson AJ, Ewing DF, Dawes EA (1990) Accumulation of polyhydroxyalkanoate containing primarily 3-hydroxydecanoate from simple carbohydrate substrates by Pseudomonas sp. strain NCIMB 40135. Appl Environ Microbiol 56:3354–3359
Hocking PJ, Marchessault RH (1994) Biopolyesters. In: Griggin GJL (ed) Chemistry and technology of biodegradable polymers. Chapman and Hall, London, pp 48–96
Hoffmann N, Steinbüchel A, Rehm BHA (2000) Homologous functional expression of cryptic phaG from Pseudomonas oleovorans establishes the transacylase-mediated polyhydroxyalkanoate biosynthetic pathway. Appl Microbiol Biotechnol 54:665–670
Holmes PA, Wright LF, Collins SH (1981) Betahydroxybutyrate polymers. Eur Patent Appl 0052459
Huijberts GN, Eggink G, de Waard P, Huisman GW, Witholt B (1992) Pseudomonas putida KT2442 cultivated on glucose accumulates poly(3-hydroxyalkanoates) consisting of saturated and unsaturated monomers. Appl Environ Microbiol 58:536–544
Huijberts GN, de Rijk TC, de Waard P, Eggink G (1994) 13C nuclear magnetic resonance studies of Pseudomonas putida fatty acid metabolic routes involved in poly(3-hydroxyalkanoate) synthesis. J Bacteriol 176:1661–1666
Huisman GW, Wonink E, Meima R, Katzemier B, Terpstra P, Witholt B (1991) Metabolism of poly(3-hydroxyalkanoates) by Pseudomonas oleovorans: identification and sequences of genes and function of the encoded proteins in the synthesis and degradation of PHA. J Biol Chem 266:2191–2198
Jaeger KE, Steinbüchel A, Jendrossek D (1995) Substrate specificities of bacterial polyhydroxyalkanoate depolymerases and lipases: bacterial lipases hydrolyze poly(β-hydroxyalkanoates). Appl Environ Microbiol 61:3113–3118
Jendrossek D (2002) Extracellular polyhydroxyalkanoate depolymeraes: the key enzymes of PHA degradation. In: Doi Y, Steinbüchel A (eds) Biopolymers, vol 3B. Polyesters II—properties and chemical synthesis. Wiley, Weinheim, pp 41–84
Jendrossek D (2005) Fluorescence microscopical investigation of poly(3-hydroxybutyrate) granule formation in bacteria. Biomacromolecules 6:598–603
Jendrossek D, Handrick R (2002) Microbial degradation of polyhydroxyalkanoates. Ann Rev Micobiol 56:403–432
Jendrossek D, Schirmer A, Schlegel HG (1996) Biodegradation of polyhydroxyalkanoic acids. Appl Microbiol Biotechnol 46:451–463
Jossek R, Steinbüchel A (1998) In vitro synthesis of poly(3-hydroxybutyric acid) by using an enzymatic coenzyme A recycling system. FEMS Microbiol Lett 168:319–324
Jurasek L, Marchessault RH (2002) The role of phasins in the morphogenesis of poly(3-hydroxybutyrate) granules. Biomacromolecules 3:256–261
Jurasek L, Marchessault RH (2004) Polyhydroxyalkanoate (PHA) granule formation in Ralstonia eutropha cells: a computer simulation. Appl Microbiol Biotechnol 64:611–617
Jurasek L, Nobes GAR, Marchessault RH (2001) Computer simulation of in vitro formation of PHB granules: particulate polymerization. Macromol Biosci 1:258–265
Kim do Y, Lütke-Eversloh T, Elbanna K, Thakor N, Steinbüchel A (2005) Poly(3-mercaptopropionate): a nonbiodegradable biopolymer? Biomacromolecules 6:897–901
Kim YB, Lenz RW, Fuller RC (1991) Preparation and characterization of poly(β-hydroxalkanoates) obtained from Pseudomonas oleovorans grown with mixtures of 5-phenylvaleric acid and n-alkanoic acids. Macromolecules 24:2324–2329
Kobayashi T, Uchino K, Abe T, Yamazaki Y, Saito T (2005) Novel intracellular 3-hydroxybutyrate-oligomer hydrolase in Wautersia eutropha H16. J Bacteriol 187:5129–5135
Korsatko VW, Wabnegg B, Tillian HM, Egger G, Pfranger R, Walser V (1984) Poly-D-(-)-3-hydroxybutyric acid — a biodegradable carrier for long term medication dosage. Studies on compatibility of poly-D-(-)-3hydroxybutyric acid implantation tablets in tissue culture and animals. Pharm Ind 46:952–954
Kunioka M, Nakamura Y, Doi Y (1988) New bacterial copolyesters produced in Alcaligenes eutrophus from organic acids. Polym Commun 29:174–176
Lee SY, Park SJ (2002) Biosynthesis and production of SCL-PHAs. In: Doi Y, Steinbüchel A (eds) Biopolymers, vol 3A. Polyesters I—biological systems and biotechnological production. Wiley, Weinheim, p 263–290
Lemoigne M (1926) Produits de deshydration et de polymerisation de lácide β-oxybutyrique. Bull Soc Chim Biol 8:770–782
Lenz RW, Kim YB, Fuller RC (1992) Production of unusual bacterial polyesters by Pseudomonas oleovorans through cometabolism. FEMS Microbiol Rev 103:207–214
Liebergesell M, Schmidt B, Steinbüchel A (1992) Isolation and identification of granule associated proteins relevant for poly(hydroxyalkanoic acid) biosynthesis in Chromatium vinosum D. FEMS Microbiol Lett 78:227–232
Liebergesell M, Sonomoto K, Madkour M, Mayer F, Steinbüchel A (1994) Purification and characterization of the poly(hydroxyalcanoic acid) synthase from Chromatium vinosum and localization of the enzyme at the surface of poly(hydroxyalkanoic acid) granules. Eur J Biochem 226:71–80
Liu SJ, Steinbüchel A (2000) Exploitation of butyrate kinase and thephosphotransbutyrase from Clostridium acetobutylicum for the in vitro biosynthesis of poly(hydroxyalkanoic acid). Appl Microbiol Biotechnol 53:545–552
Lundgren DG, Alper R, Schneitman C, Marchessault RH (1964) Characterization of poly-β-hydroxybutyrate extracted from different bacteria. J Bacteriol 89:245–251
Lütke-Eversloh T, Bergander K, Luftmann H, Steinbüchel A (2001) Bioynthesis of a new class of biopolymer: Bacterial synthesis of a sulfur containing polymer with thioester linkages. Microbiology 147:11–19
Lütke-Eversloh T, Fischer A, Remminghorst U, Kawada J, Marchessault RH, Bögershausen A, Kalwei M, Eckert H, Reichelt R, Liu SJ, Steinbüchel A (2002) Biosynthesis of novel thermoplastic polythioesters by engineered Escherichia coli. Nat Mater 1:236–240
Madison LL, Huisman GW (1999) Metabolic engineering of poly(3-hydroxyalkanoates): from DNA to plastic. Microbiol Mol Biol Rev 63:21–53
Maehara A, Doi Y, Nishiyama T, Takagi Y, Ueda S, Nakano H, Yamane T (2001) PhaR, a protein of unknown function conserved among short-chain-length polyhydroxyalkanoic acids producing bacteria, is a DNA-binding protein and represses Paracoccus denitrificans phaP expression in vitro. FEMS Microbiol Lett 200:9–15
Mayer F, Hoppert M (1997) Determination of the thickness of a boundary layer surrounding bacterial PHA inclusion bodies, and implications for models describing the molecular architecture of this layer. J Basic Microbiol 37:45–52
McCool GJ, Cannon MC (2001) PhaC and PhaR are required for polyhydroxyalkanoic acid synthase activity in Bacillus megaterium. J Bacteriol 183:4235–4243
Moldes C, Garcia P, Garcia JL, Prieto MA (2004) In vivo immobilization of fusion proteins on bioplastics by the novel tag BioF. Appl Environ Microbiol 70:3205–3212
Moskowitz GJ, Merrik JM (1969) Metabolism of poly-β-hydroxybutyrate. Enzymatic synthesis of D-(-)-β-hydroxybutyryl coenzyme A by an enoyl hydratase from Rhodospirillum rubrum. Biochemistry 8:2748–2755
Mukai K, Doi Y, Sema Y, Tomita K (1993) Substrate specificities in hydrolysis of polyhydroxyalkanoates by microbial esterases. Biotechnol Lett 15:601–604
Müller HM, Seebach D (1993) Poly(hydroxyfettsäureester), eine fünfte Klasse von physiologisch bedeutsamen organischen Biopolymeren? Angew Chem 105:483–509
Nobes GAR, Jurasek L, Marchessault RH, Martin DP, Putaux JL, Chanzy H (2000) Growth and kinetics of in vitro poly((R)-(-)-3-hydroxybutyrate) granules interpreted as particulate polymerization with coalescence. Macromol Rapid Commun 21:77–84
Oeding V, Schlegel HG (1973) β-Ketothiolase from Hydrogenomonas eutropha H16 and its significance in the regulation of poly-β-hydroxybutyrate metabolism. Biochem J 134:826–837
Peoples OP, Sinskey AJ (1989) Poly-β-hydroxybutyrate (PHB) biosynthesis in Alcaligenes eutrophus H16. Identification and characterization of the PHB polymerase gene (phbC). J Biol Chem 264:15298–15303
Pieper-Fürst U, Madkour MH, Mayer F, Steinbüchel A (1995) Identification of the region of a 14-kilodalton protein of Rhodococcus ruber that is responsible for the binding of this phasin to polyhydroxyalkanoic acid granules. J Bacteriol 177:2513–2523
Poirier Y, Gruys KJ (2002) Production of polyhydroxyalkanoates in transgenic plants. In: Doi Y, Steinbüchel A (eds) Biopolymers, vol 3A. Polyesters I—biological systems and biotechnological production. Wiley, Weinheim, pp 401–435
Pötter M, Steinbüchel A (2005) Poly(3-hydroxybutyrate) granule-associated proteins: impacts on poly(3-hydroxybutyrate) synthesis and degradation. Biomacromolecules 6:552–560
Pötter M, Madkour MH, Mayer F, Steinbüchel A (2002) Regulation of phasin expression and polyhydroxyalkanoate (PHA) granule formation in Ralstonia eutropha H16. Microbiology 148:2413–2426
Pötter M, Müller H, Reinecke F, Wieczorek R, Fricke F, Bowien B, Friedrich B, Steinbüchel A (2004) The complex structure of polyhydroxybutyrate (PHB) granules: four orthologous and paralogous phasins occur in Ralstonia eutropha. Microbiology 150:2301–2311
Pötter M, Müller H, Steinbüchel A (2005) Influence of homologous phasins (PhaP) on PHA accumulation and regulation of their expression by the transcriptional repressor PhaR in Ralstonia eutropha H16. Microbiology 151:825–833
Pries A, Priefert H, Krüger N, Steinbüchel A (1991) Identification and characterization of two Alcaligenes eutrophus gene loci relevant to the poly(β-hydroxybutyric acid)-leaky phenotype which exhibit homolohy to ptsH and ptsI of Escherichia coli. J Bacteriol 173:5843–5853
Prieto MA, Buhler B, Jung K, Witholt B, Kessler B (1999) PhaF, a polyhydroxyalkanoategranule-associated protein of Pseudomonas oleovorans GPo1 involved in the regulatory expression system for pha genes. J Bacteriol 181:858–868
Rehm BHA, Steinbüchel A (2002) PHA synthases: the key enzymes of PHA biosynthesis. In: Doi Y, Steinbüchel A (eds) Biopolymers, vol 3A. Polyesters I—biological systems and biotechnological production. Wiley, Weinheim, pp 173–216
Rehm BHA, Krüger N, Steinbüchel A (1998) A new metabolic link between fatty acid de novo synthesis and polyhydroxyalkanoic acid synthesis. The phaG gene from Pseudomonas putida KT2440 encodes a 3-hydroxyacyl-acyl carrier protein coenzyme A transferase. J Biol Chem 273:24044–24051
Reusch RN (2002) Non-storage poly-(R)-3-hydroxyalkanoates (complexed PHAs) in prokaryotes and eukaryotes. In: Doi Y, Steinbüchel A (eds) Biopolymers, vol 3A. Polyesters I—biological systems and biotechnological production. Wiley, Weinheim, pp 123–172
Saegusa H, Shiraki M, Kanai C, Saito T (2001) Cloning of an intracellular poly[D-(-)-3-hydroxybutyrate] depolymerase gene from Ralstonia eutropha H16 and characterization of the gene product. J Bacteriol 183:94–100
Saegusa H, Shiraki M, Saito T (2002) Cloning of an intracellular D(-)-3-hydroxybutyrateoligomer hydrolase gene from Ralstonia eutropha H16 and identification of the active site serine residue by site-directed mutagenesis. J Biosci Bioeng 94:106–112
Satoh Y, Minamoto N, Tajima K, Munekata M (2002) Polyhydroxyalkanoate synthase from Bacillus sp. INT005 is composed of PhaC and PhaR. J Biosci Bioeng 94:343–350
Scandola M, Forcarete ML, Frisoni G (1998) Simple kinetic model for thr heterogeneous enzymatic hydrolysis of natural poly(3-hydroxybutyrate). Macromolecules 31:3846–3851
Schlegel HG, Gottschalk G, Bartha V (1961) Formation of and utilization of poly-β-hydroxybutyric acid by knallgas bacteria (Hydrogenomonas). Nature 29:463–465
Schubert P, Steinbüchel A, Schlegel HG (1988) Cloning of the Alcaligenes eutrophus genes for synthesis of poly-β-hydroxybutyric acid (PHB) and synthesis of PHB in Escherichia coli. J Bacteriol 170:5837–5847
Schwartz E, Henne A, Cramm R, Eitinger T, Friedrich B, Gottschalk G (2003) Complete nucleotide sequence of pHG1: a Ralstonia eutropha H16 megaplasmid encoding key enzymes of H2-based lithoautotrophy and anaerobiosis. J Mol Biol 332:369–383
Senior PJ, Dawes EA (1973) The regulation of poly-β-hydroxybutyrate metabolism in Azotobacter beijerinckii. Biochem J 125:55–66
Slater SC, Voigt WH, Dennis DE (1988) Cloning and expression in Escherichia coli of the Alcaligenes eutrophus H16 poly-β-hydroxybutyrate biosynthetic pathway. J Bacteriol 170:4431–4436
Slater T, Houmiel KL, Tran M, Mitsky TA, Taylor NB, Padgette SR, Gruys KJ (1998) Multiple β-ketothiolases mediate poly(β-hydroxyalkanoate) copolymer synthesis in Ralstonia eutropha. J Bacteriol 180:1979–1987
Steinbüchel A (1991) Polyhydroxyalkanoic acids. NATO AEW: novel materials from biological sources. In: Byrom D (ed) Biomaterials. MacMillan, London, pp 123–213
Steinbüchel A (2001) Perspectives for biotechnological production and utilization of biopolymers: metabolic engineering of polyhydroxyalkanoate biosynthesis pathways as a successful example. Macromol Biosci 1:1–24
Steinbüchel A, Schlegel HG (1989) Excretion of pyruvate by mutants of Alcaligenes eutrophus, which are impaired in the accumulation of poly(β-hydroxybutyric acid) (PHB), under conditions permissive for synthesis of PHB. Appl Microbiol Biotechnol 31:168–175
Steinbüchel A, Füchtenbusch B (1998) Bacterial and other biological systems for polyester production. Trends Biotechnol 16:419–427
Steinbüchel A, Valentin HE (1995) Diversity of microbial polyhydroxyalkanoic acids. FEMS Microbiol Lett 128:219–228
Steinbüchel A, Hustede E, Liebergesell M, Pieper U, Timm A, Valentin H (1992) Molecular basis for biosynthesis and accumulation of polyhydroxyalkanoic acids in bacteria. FEMS Microbiol Rev 9:217–230
Steinbüchel A, Aerts K, Babel W, Föllner C, Liebergesell M, Madkour MH, Mayer F, Pieper-Fürst U, Pries A, Valentin HE, Wieczorek R (1995) Considerations on the structure and biochemistry of bacterial polyhydroxyalkanoic acid inclusions. Can J Microbiol 41:94–105
Stuart ES, Tehrani A, Valentin HE, Dennis D, Lenz RW, Fuller RC (1998) Protein organization on the PHA inclusion cytoplasmic boundary. J Biotechnol 64:137–144
Stubbe J, Tian J (2003) Polyhydroxyalkanoate (PHA) homeostasis: the role of the PHA synthase. Nat Prod Rep 20:445–457
Sudesh K, Maehara A, Gan Z, Iwata T, Doi Y (2004) Direct observation of polyhydroxyalkanoate granule-associated-proteins on native granules and on poly(3-hydroxybutyrate) single crystals by atomic force microscopy. Polym Degrad Stab 83:281–287
Srinivasan S, Barnard GC, Gerngross TU (2002) A novel high-cell-density protein expression system based on Ralstonia eutropha. Appl Environ Microbiol 68:5925–5932
Taguchi K, Taguchi S, Sudesh K, Maehara A, Tsuge T, Doi Y (2002) Metabolic pathways and engineering of PHA biosynthesis. In: Doi Y, Steinbüchel A (eds) Biopolymers, vol 3A. Polyesters I—biological systems and biotechnological production. Wiley, Weinheim, pp 217–248
Tian J, Sinskey AJ, Stubbe J (2005a) Kinetic studies of polyhydroxybutyrate granule formation in Wautersia eutropha H16 by transmission electron microscopy. J Bacteriol 187:3814–3824
Tian J, He A, Lawrence AG, Liu P, Watson N, Sinskey AJ, Stubbe J (2005b) Analysis of transient polyhydroxybutyrate production in Wautersia eutropha H16 by quantitative Western analysis and transmission electron microscopy. J Bacteriol 187:3825–3832
Timm A, Steinbüchel A (1990) Formation of polyesters consisting of medium-chain-length 3-hydroxyalkanoic acids from gluconate by Pseudomonas aeruginosa and other fluorescent pseudomonads. Appl Environ Microbiol 56:3360–3367
Tsuge T, Fukui T, Matsusaki H, Taguchi S, Kobayashi G, Ishizak A, Doi Y (2000) Molecular cloning of two (R)-specific enoyl-CoA hydratase genes from Pseudomonas aeruginosa and their use for polyhydroxyalkanoate synthesis. FEMS Microbiol Lett 184:193–208
Valentin H, Schönebaum A, Steinbüchel A (1992) Identification of 4-hydroxyvaleric acid as a constituent in biosynthetic polyhydroxyalkanoic acids from bacteria. Appl Microbiol Biotechnol 36:507–514
Valentin HE, Zwingmann G, Schönebaum A, Steinbüchel A (1995) Metabolic pathway for biosynthesis of poly(3-hydroxybutyrate-co-4-hydroxybutyrate) from 4-hydroxybutyrate by Alcaligenes eutropha. Eur J Biochem 227:43–60
Wältermann M, Steinbüchel A (2005) Neutral lipid bodies in prokaryotes: recent insights into structure, formation, and relationship to eukaryotic lipid depots. J Bacteriol 187:3607–3619
Wältermann M, Hinz A, Robenek H, Troyer D, Reichelt R, Malkus U, Galla HJ, Kalscheuer R, Stöveken T, von Landenberg P, Steinbüchel A (2005) Mechanism of lipid-body formation in prokaryotes: how bacteria fatten up. Mol Microbiol 55:750–763
Weusthuis RA, Kessler B, Dielissen MPM, Witholt B, Eggink G (2002) Fermentative production of medium-chain-length poly(3-hydroxyalkanoate). In: Doi Y, Steinbüchel A (eds) Biopolymers, vol 3A. Polyesters I—biological systems and biotechnological production. Wiley, Weinheim, pp 291–316
Wieczorek R, Pries A, Steinbüchel A, Mayer F (1995) Analysis of a 24-kilodalton protein associated with the polyhydroxyalkanoic acid granules in Alcaligenes eutrophus. J Bacteriol 177:2425–2435
Williams SF, Martin DP (2002) Applications of PHAs in medicine and pharmacy. In: Doi Y, Steinbüchel A (eds) Biopolymers, vol 4. Polyesters III—applications and commercial products. Wiley, Weinheim, pp 91–127
Williams SF, Martin DP, Horowitz DM, Peoples OP (1999) PHA applications: addressing the price performance issue I. Tissue engineering. Int J Biol Macromol 25:111–121
Williamson DH, Wilkinson JF (1958) The isolation and estimation of poly-β-hydroxybutyrate inclusions of Bacillus species. J Gen Microbiol 19:198–209
York GM, Junker BH, Stubbe J, Sinskey AJ (2001a) Accumulation of the PhaP phasin of Ralstonia eutropha is dependent on production of polyhydroxybutyrate in cells. J Bacteriol 183:4217–4226
York GM, Stubbe J, Sinskey AJ (2001b) New insight into the role of the PhaP phasin of Ralstonia eutropha in promoting synthesis of polyhydroxybutyrate. J Bacteriol 183:2394–2397
York GM, Stubbe J, Sinskey AJ (2002) The Ralstonia eutropha PhaR protein couples synthesis of the PhaP phasin to the presence of polyhydroxybutyrate in cells and promotes polyhydroxybutyrate production. J Bacteriol 184:59–66
York GM, Lupberger J, Tian JM, Lawrence AG, Stubbe J, Sinskey AJ (2003) Ralstonia eutropha H16 encodes two and possibly three intracellular poly[D-(-)-3-hydroxybutyrate] depolymerase genes. J Bacteriol 185:3788–3794
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Pötter, M., Steinbüchel, A. (2006). Biogenesis and Structure of Polyhydroxyalkanoate Granules. In: Shively, J.M. (eds) Inclusions in Prokaryotes. Microbiology Monographs, vol 1. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-33774-1_5
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