Skip to main content
Log in

Polyhydroxyalkanoate (PHA) granule formation in Ralstonia eutropha cells: a computer simulation

  • Mini-Review
  • Published:
Applied Microbiology and Biotechnology Aims and scope Submit manuscript

Abstract

Computer simulation of polyhydroxyalkanoate (PHA) granule formation in vivo could help to design strategies to optimize the fermentation process and achieve higher yields of PHA. It could also suggest biotechnological approaches to control the granule size and molecular weight of the polymer. A computer program simulating the formation of PHA granules inside a Ralstonia eutropha cell was developed, based on published experimental data. The results are applicable to R. eutropha cells or other microorganisms and transgenic plants, where polyhydroxybutyrate production is made possible by heterologous expression systems. The simulation starts at the outset of the PHA accumulation phase when the cells are small and contain no PHA granules. In the presence of abundant glucose, the cell responds to phosphorus limitation by producing 3-hydroxybutyryl-CoA which undergoes polymerization on the few PHA synthase molecules present in the cytoplasm. The amphiphilic PHA synthase–PHA complex attracts additional PHA synthase molecules and granules begin to grow from these initiation sites. Phosphorus limitation and the appearance of PHA in the cytoplasm also stimulate production of phasin molecules that attach themselves to the growing granules. As the granules grow bigger, they begin to touch each other and move to optimize their packing. The phasin coat prevents the granules from coalescing. The size of the cell increases and its prolate ellipsoid shape becomes closer to spherical. The accumulation process stops either when the supply of glucose is exhausted or when the granules become tightly packed within the cell, so that access to their surface is limited. All important variables, such as cell dimensions, granule size, counts of granule-associated molecules, PHA yield, degree of polymerization of the PHA molecules, etc., are recorded in real time during the simulation. Examples of virtual experiments with the cell and their results are shown.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  • Anderson AJ, Dawes EA (1990) Occurrence, metabolism, metabolic role, and industrial uses of bacterial polyhydroxyalkanoates. Microbiol Rev 54:450–472

    Google Scholar 

  • Ballard DGH, Holmes PA, Senior PJ (1987) Formation of polymers of β-hydroxybutyric acid in bacterial cells and a comparison of the morphology of growth with the formation of polyethylene in the solid state. Recent Adv Mech Synth Aspects Polym 1987:293–314

    Google Scholar 

  • 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

    Google Scholar 

  • Carballido-López R, Errington J (2003) A dynamic bacterial cytoskeleton. Trends Cell Biol 13:577–583

    Google Scholar 

  • Clemente T, Shah D, Tran M, Stark D, Padgette S, Dennis D, Bruckener K, Steinbüchel A, Mitsky T (2000) Sequence of PHA synthase gene from two strains of Rhodospirillum rubrum and in vivo substrate specificity of four PHA synthases across two heterologous expression systems. Appl Microbiol Biotechnol 53:420–429

    Google Scholar 

  • Doi Y, Kawaguchi Y, Koyama N, Nakamura S, Hiramitsu M, Yoshida Y, Kimura H (1992) Synthesis and degradation of polyhydroxyalkanoates in Alkaligenes eutrophus. FEMS Microbiol Rev 103:103–108

    Google Scholar 

  • Ellar D, Lundgren DG, Okamura K, Marchessault RH (1968) Morphology of poly-β-hydroxybutyrate granules. J Mol Biol 35:489–502

    Google Scholar 

  • Gorenflo V, Schmack G, Vogel R, Steinbüchel A (2001) Development of a process for the biotechnological large-scale production of 4-hydroxyvalerate-containing polyesters and characterization of their physical and mechanical properties. Biomacromolecules 2:45–57

    Google Scholar 

  • Grothe E, Moo-Young M, Chisti Y (1999) Fermentation optimization for the production of poly(β-hydroxybutyric acid) microbial thermoplastic. Enzyme Microb Technol 25:132–141

    Google Scholar 

  • Hänggi UJ (1990) Pilot scale production of PHB with Alcaligenes latus. In: E.A. Dawes (ed) Novel biodegradable microbial polymers. Kluwer, Dordrecht, pp 65–70

  • Hoppert M, Mayer F (1999) Principles of macromolecular organization and cell function in bacteria and archaea. Cell Biochem Biophysiol 31:247–284

    Google Scholar 

  • Hustede E, Steinbüchel A, Schlegel HG (1992) Cloning of poly(3-hydroxybutyric acid) synthase genes of Rhodobacter sphaeroides and Rhodospirillum rubrum and heterologous expression in Alcaligenes eutrophus. FEMS Microbiol Lett 72:285–290

    Google Scholar 

  • Ingraham JL, Maaloe O, Neidhardt FC (1983) Growth of the bacterial cell. Sinauer Associates, Sunderland, Mass.

  • Jendrossek D, Handrick R (2002) Microbial degradation of polyhydroxyalkanoates. Annu Rev Microbiol 56:403–432

    Google Scholar 

  • Jossek R, Reichelt R, Steinbüchel A (1998) In vitro biosynthesis of poly(3-hydroxybutyric acid) by using purified poly(hydroxyalkanoic acid) synthase of Chromatium vinosum. Appl Microbiol Biotechnol 49:258–266

    Google Scholar 

  • Jung K, Hazenberg W, Prieto M, Witholt B (2001) Two-stage continuous process development for the production of medium-chain-length poly(3-hydroxyalkanoates). Biotechnol Bioeng 72:19–24

    Google Scholar 

  • Jurasek L, Marchessault RH (2002) The role of phasins in the morphogenesis of poly(3-hydroxybutyrate) granules. Biomacromolecules 3:256–261

    Google Scholar 

  • Jurasek L, Nobes GAR, Marchessault RH (2001) Computer simulation of in vitro formation of PHB granules: particulate polymerization. Macromol Biosci 1:258–265

    Google Scholar 

  • Kawaguchi Y, Doi Y (1992) Kinetics and mechanism of synthesis and degradation of poly-(3-hydroxybutyrate) in Alkaligenes eutrophus. Macromolecules 25:2324–2329

    Google Scholar 

  • Koizumi F, Abe H, Doi Y (1995) Molecular weight of poly(3-hydroxybutyrate) during biological polymerization in Alkaligenes eutrophus. J Macromol Sci Pure Appl Chem A32:759–774

    Google Scholar 

  • Korotkova N, Chistoserdova L, Lidstrom ME (2002) Poly-β-hydroxybutyrate biosynthesis in the facultative methylotroph Methylobacterium extorquens AM1: identification and mutation of gap11, gap20, and phaR. J Bacteriol 184:6174–6181

    Google Scholar 

  • Kurja J, Koning GM de, Zirkzee HF, Maxwell IA (1994) A new kinetic model for the accumulation of poly-3-hydroxybutyrate in Alcaligenes eutrophus. Granule formation and granule growth. Stud Polym Sci 12:379–386

    Google Scholar 

  • Ma CK, Chua H, Yu PHF, Hong K (2000) Optimal production of polyhydroxyalkanoates in activated sludge biomass. Appl Biochem Biotechnol 84/86:981–989

    Google Scholar 

  • Maehara A, Ueda S, Nakano H, Yamane T (1999) Analyses of a polyhydroxyalkanoic acid granule-associated 16-kilodalton protein and its putative regulator in the pha locus of Paracoccus denitrificans. J Bacteriol 181:2914–2921

    Google Scholar 

  • Maehara A, Taguchi S, Nishiyama T, Yamane T, Doi Y (2002) A repressor protein, PhaR, regulates polyhydroxyalkanoate (PHA) synthesis via its direct interaction with PHA. J Bacteriol 184:3992–4002

    Google Scholar 

  • Mantzaris NV, Kelley AS, Daoutidis P, Srienc F (2002) A population balance model describing the dynamics of molecular weight distributions and the structure of PHA copolymer chains. Chem Eng Sci 57:4643–4663

    Google Scholar 

  • Mayer F, Madkour MH, Pieper-Fürst U, Wieczorek R, Liebergesell M, Steinbüchel A (1996) Electron microscopic observations on the macromolecular organization of the boundary layer of bacterial PHA inclusion bodies. J Gen Appl Microbiol 42:445–455

    Google Scholar 

  • Mayer F, Vogt B, Poc C (1998) Immunoelectron microscopic studies indicate the existence of a cell shape preserving cytoskeleton in prokaryotes. Naturwissenschaften 85:278–282

    Google Scholar 

  • Pedros-Alio C, Mas J, Guerero R (1985) The influence of polyhydroxyalkanoate accumulation on cell volume and buoyant density in Alcaligenes eutrophus. Arch Microbiol 143:178–184

    Google Scholar 

  • 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

    Google Scholar 

  • Saegusa H, Shiraki M, Saoito T (2002) Cloning of an intracellular d(−)-3-hydroxybutyrate-oligomer hydrolase gene from Ralstonia eutropha H16 and identification of the active site serine residue by site-directed mutagenesis. J Biosci Bioeng 94:106–112

    Google Scholar 

  • Sim SJ, Snell KD, Hogan SA, Stubbe JA, Rha C, Sinskey AJ (1997) PHA synthase activity controls the molecular weight and polydispersity of polyhydroxybutyrate in vivo. Nat Biotechnol 15:63–67

    Google Scholar 

  • Steinbüchel A, Aerts K, Babel W, Föllner C, Liebergesell M, Madkour MH, Mayer F, Pieper-Fürst U, Pries A, Valentin HE, Wieczorek R (1995) Consideration on the structure and biochemistry of bacterial polyhydroxyalkanoic acid inclusions. Can J Microbiol 41[Suppl 1]:94–105

  • Stuart ES, Tehrani A, Valentin HE, Dennis D, Lenz RW, Fuller RC (1998) Protein organization on the inclusion cytoplasmic boundary. J Biotechnol 64:137–144

    Google Scholar 

  • Taguchi S, Matsusaki H, Matsumoto K, Takase K, Taguchi K, Doi Y (2002) Biosynthesis of biodegradable polyesters from renewable carbon sources by recombinant bacteria. Polym Int 51:899–906

    Google Scholar 

  • 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

    Google Scholar 

  • York GM, Junker BH, Stubbe J-A, Sinskey AJ (2001) Accumulation of the PhaP phasin of Ralstonia eutropha is dependent on production of polyhydroxybutyrate in cells. J Bacteriol 183:4217–4226

    Google Scholar 

  • Zhang S, Yasuo T, Lenz RW, Goodwin S (2000) Kinetic and mechanistic characterization of the polyhydoxybutyrate synthase from Ralstonia eutropha. Biomacromolecules 1:244–251

    Google Scholar 

Download references

Acknowledgements

A survey of experts in the field of polyhydroxyalkanoates provided us with invaluable help in compiling the computer simulation. We wish to thank in particular Prof. F.S. Archibald, Prof. Y. Doi, Prof. R.C. Fuller, Prof. R.W. Lenz, Prof. F. Mayer, Prof. T. Saito, and Prof. A. Steinbüchel for their advice.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to R. H. Marchessault.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Jurasek, L., Marchessault, R.H. Polyhydroxyalkanoate (PHA) granule formation in Ralstonia eutropha cells: a computer simulation. Appl Microbiol Biotechnol 64, 611–617 (2004). https://doi.org/10.1007/s00253-003-1551-9

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00253-003-1551-9

Keywords

Navigation