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Unbalanced growth as a normal feature of development of Bdellovibrio bacteriovorus

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Abstract

In this study we have investigated the rates and spatial patterns of chromosome replication and cell elongation during the growth phase of wild-type and facultatively prey-independent mutant strains of Bdellovibrio bacteriovorus. For the facultatively prey-independent mutants, the total DNA content of synchronously growing cultures was found to increase exponentially, as the multiple chromosomes within each filamentous cell replicated simultaneously. Cell mass, measured as total cellular protein, also increased exponentially during this period, apparently by means of multiple elongation sites along the filament wall. The relative rates of DNA and protein synthesis were unbalanced during growth, however, with the cellular concentration of DNA increasing slightly faster than that of protein. The original cellular DNA: protein ratio was restored in the progeny cells by continued protein synthesis during the septation period that follows the termination of DNA replication. Because of technical problems, these experiments could not be conducted on the wild-type cells, but similar results are assumed. This unusual pattern of unbalanced growth may represent an adaptation by bdellovibrios to maximize their progeny yield from the determinate amount of substrate available within a given prey cell.

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References

  • Baldwin WW, Wegener WS (1986) Kinetics of Gram-negative bacterial cell elongation as measured by using the large rod “Lineola longa”. J Bacteriol 166:435–438

    Google Scholar 

  • Burman LG, Raichler J, Park JT (1983) Evidence for diffuse growth of the cylindrical portion of the Escherichia coli murein sacculus. J Bacteriol 155:983–988

    Google Scholar 

  • Burnham JC, Hashimoto T, Conti SF (1970) Ultrastructure and cell division of a facultatively parasitic strain of Bdellovibrio bacteriovorus. J Bacteriol 101:997–1004

    Google Scholar 

  • Burton K (1956) A study of the conditions and the mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid. Biochem J 62:315–323

    Google Scholar 

  • Caro LG (1964) High-resolution autoradiography. In: Prescott DM (ed) Methods in cell physiology, vol 1. Academic Press, New York, pp 327–363

    Google Scholar 

  • Cooper S (1988) What is the bacterial growth law during the division cycle? J Bacteriol 170:5001–5005

    Google Scholar 

  • Donachie WD (1968) Relationship between cell size and time of initiation of DNA replication. Nature 219:1077–1079

    Google Scholar 

  • Eksztejn M, Varon M (1977) Elongation and cell division in Bdellovibrio bacteriovorus. Arch Microbiol 114:175–181

    Google Scholar 

  • Grossman M, Ron EZ (1980) Initiation of deoxyribonucleic acid replication in Escherichia coli B: Uneoupling from mass/deoxyribonucleic acid ratio. J Bacteriol 143:100–104

    Google Scholar 

  • Hespell RB, Thomashow MF, Rittenberg SC (1974) Changes in cell composition and viability of Bdellovibrio bacteriovorus during starvation. Arch Microbiol 97:313–327

    Google Scholar 

  • Horowitz AT, Kessel M, Shilo M (1974) Growth cycle of predacious bdellovibrios in a host-free extract system and some properties of the host extract. J Bacteriol 117:270–282

    Google Scholar 

  • Kessel M, Shilo M (1976) Ralationship of Bdellovibrio elongation and fission to host cell size. J Bacteriol 128:477–480

    Google Scholar 

  • Koch AL (1988) Biophysics of bacterial walls viewed as stressbearing fabric. Microbiol Rev 52:337–353

    Google Scholar 

  • Koppes LJH, Meyer M, Oonk HB, DeJong MA, Nanninga N (1980) Correlation between size and age at different events in the cell division cycle of Escherichia coli. J Bacteriol 143:1241–1252

    Google Scholar 

  • Kubitscheck HE (1981) Bilinear cell growth of Escherichia coli. J Bacteriol 148:730–733

    Google Scholar 

  • Mazia D, Schatten G, Sale W (1975) Adhesion of cells to surfaces coated with polylysine. J Cell Biol 66:198–200

    Google Scholar 

  • Peterson GL (1979) Review of the Folin protein quantitation method of Lowry, Rosebrough, Farr and Randall. Anal Biochem 100:201–220

    Google Scholar 

  • Rittenberg SC (1982) Bdellovibrios-intraperiplasmic growth. In: Burns RG, Slater JH (eds) Experimental microbial ecology. Backwell, Oxford, pp 379–382

    Google Scholar 

  • Rittenberg SC (1983) Bdellovibrio: Attack, penetration, and growth on its prey. ASM News 49:435–439

    Google Scholar 

  • Ruby EG, Rittenberg SC (1983) Differentiation after premature release of intraperiplasmically growing Bdellovibrio bacteriovorus. J Bacteriol 154:32–40

    Google Scholar 

  • Ruby EG, McCabe JB, Barke JI (1985) Uptake of intact nucleoside monophosphates by Bdellovibrio bacteriovorus 109J. J Bacteriol 163:1087–1094

    Google Scholar 

  • Schwartz U, Asmus A, Frank H (1969) Autolytic enzymes and cell division of Escherichia coli. J Mol Biol 43:419–429

    Google Scholar 

  • Seidler RJ, Starr MP (1969) Isolation and characterization of hostindependent bdellovibrios. J Bacteriol 100:769–785

    Google Scholar 

  • Thomashow MF, Rittenberg SC (1978) Intraperiplasmic growth of Bdellovibrio bacteriovorus 109J: Solubilization of Escherichia coli peptidoglycan. J Bacteriol 135:998–1007

    Google Scholar 

  • Whitaker JR, Granum PE (1980) An absolute method for protein determination based on difference in absorbance at 235 and 280 nm. Anal Biochem 109:156–159

    Google Scholar 

  • Woldringh CL, Huls P, Pas E, Brackenhoff GJ, Nanninga N (1987) Topography of peptidoglycan synthesis during elongation and polar cap formation in a cell division mutant of Escherichia coli MC4100. J Gen Microbiol 133:575–586

    Google Scholar 

  • Zaritsky A, Zabrovitz S (1981) DNA synthesis in Escherichia coli during a nutritional shift-up. Mol Gen Genet 181:564–566

    Google Scholar 

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Gray, K.M., Ruby, E.G. Unbalanced growth as a normal feature of development of Bdellovibrio bacteriovorus . Arch. Microbiol. 152, 420–424 (1989). https://doi.org/10.1007/BF00446922

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  • DOI: https://doi.org/10.1007/BF00446922

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