Effect of poly(3-hydroxybutyrate) (PHB) content on the starvation-survival of bacteria in natural waters

The effect of poly(3-hydroxybutyrate) (PHB) content on the survival of wild-type strains and PHB negative mutants of Bacillus megaterium and Alcaligenes eutrophus in natural waters was studied. The survival strategy of B. megaterium was dominated by the development of resistant forms, but the number...

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Autor principal: Lopez, N.I
Otros Autores: Floccari, M.E, Steinbuchel, A., Garcia, A.F, Mendez, B.S
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 1995
Acceso en línea:Registro en Scopus
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030 |a FMECE 
100 1 |a Lopez, N.I. 
245 1 0 |a Effect of poly(3-hydroxybutyrate) (PHB) content on the starvation-survival of bacteria in natural waters 
260 |c 1995 
270 1 0 |m Méndez, B.S.; Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, 1428 Buenos Aires, Argentina 
506 |2 openaire  |e Política editorial 
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504 |a Steinbüchel, Polyhydroxyalkanoic acids (1991) Biomaterials, pp. 123-213. , D. Byrom, Macmillan Publishers Ltd., Basingstoke, UK 
504 |a Steinbüchel, Hustede, Liebergesell, Pieper, Tim, Valentin, Molecular basis for biosynthesis and accumulation of polyhydroxyalkanoic acids in bacteria (1992) FEMS Microbiol. Rev., 103, pp. 217-230 
504 |a Matin, Veldhuis, Stegeman, Veenhuis, Selective advantage of a Spirillum sp. in a carbon-limited environment. Accumulation of poly-β-hydroxybutyric acid and its role in starvation (1979) J. Gen. Microbiol., 112, pp. 349-355 
504 |a Findlay, White, Polymeric beta-hydroxyalkanoates from environmental samples and Bacillus megaterium (1983) Appl. Environ. Microbiol., 45, pp. 71-78 
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504 |a Kjelleberg, Albertson, Flardh, Holmquist, Jouper-Jaan, Marouga, Ostling, Weichart, How do non-differentiating bacteria adapt to starvation? (1993) Antonie van Leeuwenhoek, 63, pp. 333-341 
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504 |a Henrysson, McCarty, Influence of the endogenous storage lipid poly-β-hydroxybutyrate on the reducing power availability during cometabolism if trichloroethylene and naphtalene by resting methanotrophic mixed cultures (1993) Appl. Environ. Microbiol., 59, pp. 1602-1606 
504 |a Dawes, Senior, The role and regulation of energy reserve polymers in micro-organisms (1973) Adv. Microb. Physiol., 10, pp. 135-266 
504 |a Okon, Itzigsohn, Poly-β-hydroxybutyrate metabolism in Azospirillum brasilense and the ecological role of PHB in the rhizosphere (1992) FEMS Microbiol. Rev., 103, pp. 131-141 
504 |a Braunegg, Sonnleitner, Lafferty, A rapid gas chromatographic method for the determination of poly-3-hydroxybutyric acid in microbial biomass (1978) Eur. J. Microbiol. Biotechnol., 6, pp. 29-37 
504 |a Brandl, Gross, Lenz, Fuller, Pseudomonas oleovorans as a source of poly-(β-hydoxyal-kanoate) for potential applications biodegradable polyesters (1988) Appl. Environ. Microbiol., 54, pp. 1977-1982 
504 |a Tao, Vary, Isolation and characterization of a sporulation lacZ fusion mutants of Bacillus megaterium (1991) J. Gen. Microbiol., 137, pp. 797-806 
504 |a Floccari, Tiscornia, Palmada, Méndez, Enriquecimiento en mutantes de Bacillus megaterium deficientes en la síntesis de poli(3-hidroxibutirato) (1991) Rev. Arg. Microbiol., 23, pp. 14-25 
504 |a Srivastava, Urban, Friedrich, Mutagenesis of Alcaligenes eutrophus by insertion of the drug-resistence transposon Tn5 (1982) Arch. Mikrobiol., 131, pp. 203-207 
504 |a Schlegel, Lafferty, Krauss, The isolation of mutants not accumulating poly-β-hydroxybutyric acid (1970) Archiv f�r Mikrobiologie, 74, pp. 283-294 
504 |a Schubert, Steinbüchel, Schlegel, Cloning of the Alcaligenes eutrophus genes for synthesis of poly-β-hydroxybutyric acid (PHB) and synthesis of PHB in Escherichia coli (1988) J. Bacteriol., 170, pp. 5837-5847 
504 |a Vary, Garbe, Franzen, Frampton, MP13, a generalized transducing bacteriophage for Bacillus megaterium (1982) J. Bacteriol., 149, pp. 1112-1119 
504 |a Ostle, Holt, Nile Blue A as a fluorescent stain for poly-β-hydroxybutyrate (1982) Appl. Environ. Microbiol., 44, pp. 238-241 
504 |a Bohall, Jr., Vary, Transposition of Tn917 in Bacillus megaterium (1986) J. Bacteriol., 167, pp. 716-718 
504 |a Clewell, Gawron-Burke, Conjugative transposons and the dissemination of antibiotic resistance in streptococci (1988) Annual Review of Microbiology, 40, pp. 635-665 
504 |a Reznikoff, The Tn5 transposon (1993) Ann. Rev. Microbiol., 47, pp. 945-963 
504 |a Priest, Isolation and identification of aerobic endospore-forming bacteria (1989) Bacillus. Biotechnology Handbooks, pp. 293-320. , C.R. Harwood, Plenum Press, New York 
504 |a Strauch, Hoch, Transition-state regulators: sentinels of Bacillus subtilis post-exponential gene expression (1993) Mol. Microbiol., 7, pp. 337-342 
504 |a Slepecky, Law, Synthesis and degradation of poly-β-hydroxybutyric acid in connection with sporulation of Bacillus megaterium (1961) J Bacteriol, 82, pp. 37-42 
504 |a Recorbet, Givaudan, Steinberg, Bally, Normand, Faurie, Tn5 to assess soil fate of genetically marked bacteria: screening for aminoglycoside-resistence advantage and labelling specificity (1992) FEMS Microbiol. Ecol., 86, pp. 187-194 
504 |a Garcia-Lara, Martinez, Vilamú, Vives-Rego, Effect of previous growth conditions on the starvation-survival of Escherichia coli in seawater (1993) J. Gen. Microbiol., 139, pp. 1425-1431 
504 |a Hippe, Abbau und Wiederverwertung von Poly-β-hydroxybuttersäure durch Hydrogenomonas H16 (1967) Arch. Mikrobiol., 56, pp. 248-277 
520 3 |a The effect of poly(3-hydroxybutyrate) (PHB) content on the survival of wild-type strains and PHB negative mutants of Bacillus megaterium and Alcaligenes eutrophus in natural waters was studied. The survival strategy of B. megaterium was dominated by the development of resistant forms, but the number of the wild-type vegetative cells was higher than that of PHB mutant strain. In some environmental conditions the mutant spores needed a heat shock for germination, a fact that suggests, for the first time, that PHB plays a role in this phenomenon. Survival of A. eutrophus wild-type strain in all experiments was higher compared to the PHB mutant, and differences were significant. In raw river water, survival of both species was lower than in sterile river water. © 1995.  |l eng 
536 |a Detalles de la financiación: This work was supported by grants from the Consejo National de Investigaciones Cientificas y Tecnicas (CONICET, Argentina). N.I.L. has a postdoctoral fellowship from CONICET. 
593 |a Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, 1428 Buenos Aires, Argentina 
593 |a Cátedra de Microbiología, Facultad de Agronomía, Universidad de Buenos Aires, Buenos Aires, Argentina 
593 |a Institut für Mikrobiologie, Georg-August-Universität Göttingen, Göttingen, Germany 
690 1 0 |a ENVIRONMENTAL SURVIVAL 
690 1 0 |a POLY(3-HYDROXYBUTYRATE) MUTANT 
690 1 0 |a SPORE GERMINATION 
690 1 0 |a POLY(3 HYDROXYBUTYRIC ACID) 
690 1 0 |a ARTICLE 
690 1 0 |a BACILLUS MEGATERIUM 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a NONHUMAN 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a SPORE GERMINATION 
690 1 0 |a SURVIVAL 
690 1 0 |a WAUTERSIA EUTROPHA 
690 1 0 |a ALCALIGENES 
690 1 0 |a BACILLUS MEGATERIUM 
690 1 0 |a WAUTERSIA EUTROPHA 
700 1 |a Floccari, M.E. 
700 1 |a Steinbuchel, A. 
700 1 |a Garcia, A.F. 
700 1 |a Mendez, B.S. 
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