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Extracellular Hydrolytic Enzymes Produced by Moderately Halophilic Bacteria

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Halophilic Microorganisms

Abstract

High salinity is the main characteristic of hypersaline habitats, in which the salt concentration is generally higher than that of seawater. Among the beststudied hypersaline environments are the saline lakes (Dead Sea, Great Salt Lake), salterns used for the production of salt and some saline soils. Except for a few eukaryotic organisms such as the brine shrimp (Artemia salina) or the photosynthetic flagellate Dunaliella, most organisms adapted to live in these hypersaline environments are prokaryotic microorganisms belonging to the groups of archaea and bacteria (Rodríguez-Valera 1993). The salt requirements divide these populations of prokaryotic halophilic microorganisms into two predominant physiological groups: extreme halophiles, which grow optimally in media containing 15–30% NaCl, and moderate halophiles, which are able to grow optimally in media containing between 3 and 15% NaCl. Highly saline environments are dominated by extremely halophilic archaea, mostly halobacteria. However, in the intermediate salinities, the most abundant microorganisms are the moderate halophiles, a heterogeneous group which includes very different Gram-negative and Gram-positive bacterial species, as well as some archaea (Ventosa et al.1998).

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References

  • Amann RI, Ludwig W, Schleifer KH (1995) Phylogenetic identification and in situ detec- tion of individual microbial cells without cultivation. Microbiol Rev 59: 143–169

    PubMed  CAS  Google Scholar 

  • Coronado MJ, Vargas C, Hofemeister J, Ventosa A, Nieto JJ (2000a) Production and biochemical characterization of an a-amylase from the moderate halophile Halomonas meridiana. FEMS Microbiol Lett 183: 67–71

    PubMed  CAS  Google Scholar 

  • Coronado MJ, Vargas C, Mellado E, Tegos G, Drainas C, Nieto JJ, Ventosa A (2000b) The a-amylase gene amyH of the moderate halophile Halomonas meridiana: cloning and molecular characterization. Microbiology 146: 861–868

    PubMed  CAS  Google Scholar 

  • Da Costa MS, Santos H, Galinski EA (1997) An overview of the role and diversity of compatible solutes in bacteria and archaea. In: Scheper TH (ed) Advances in biochemical engineering/biotechnology, vol 61. Springer, Berlin Heidelberg New York, pp 117–153

    Google Scholar 

  • Frillingos S, Linden A, Niehaus F, Vargas C, Nieto JJ, Ventosa A, Antranikian G, Drainas C (2000) Cloning and expression of a-amylase from the hyperthermophilic archaeon Pyrococcus woesei in the moderately halophilic bacterium Halomonas elongata. J Appl Microbiol 88: 495–503

    Article  PubMed  CAS  Google Scholar 

  • Henrissat B (1991) A classification of glycosyl hydrolases based on amino acid sequence similarities. Biochem J 280: 309–316

    PubMed  CAS  Google Scholar 

  • Henrissat B, Bairoch A (1993) New families in the classification of glycosyl hydrolases based on amino acid sequence similarities. Biochem J 293: 781–788

    PubMed  CAS  Google Scholar 

  • Kamekura M (1986) Production and function of enzymes of eubacterial halophiles. FEMS Microbiol Rev 39: 145–150

    Article  CAS  Google Scholar 

  • Kamekura M, Onishi H (1978) Properties of the halophilic nuclease of a moderate halophile, Micrococcus varians subsp. halophilus. J Bacteriol 133: 59–65

    PubMed  CAS  Google Scholar 

  • Kamekura M, Onishi H (1983) Inactivation of nuclease H of the moderate halophile Micrococcus varians subsp. halophilus during cultivation in the presence of salting-in type salts. Can J Microbiol 29: 46–51

    Article  CAS  Google Scholar 

  • Kamekura M, Hamakawa T, Onishi H (1982) Application of halophilic nuclease H of Micrococcus varians subsp. halophilus to commercial production of flavoring agent 5¢-GMP. Appl Environ Microbiol 44: 994–995

    PubMed  CAS  Google Scholar 

  • Khire JM (1994) Production of moderately halophilic amylase by newly isolated Micro-coccus sp. 4 from a salt pan. Lett Appl Microbiol 19: 210–212

    Article  CAS  Google Scholar 

  • Kobayashi T, Kamekura M, Kanlayakrit W, Onishi H (1986) Production, purification and characterization of an amylase of the moderate halophile, Micrococcus varians subsp. halophilus. Microbios 46: 165–170

    CAS  Google Scholar 

  • Margesin R, Schinner F (2001) Potential of halotolerant and halophilic microorganisms for biotechnology. Extremophiles 5: 73–83

    Article  PubMed  CAS  Google Scholar 

  • Mota RR, Marquez MC, Arahal DR, Mellado E, Ventosa A (1997) Polyphasic taxonomy of Nesterenkonia halobia. Int J Syst Bacteriol 47: 1231–1235

    Article  PubMed  CAS  Google Scholar 

  • Nakajima R, Imanaka T, Aiba S (1986) Comparison of amino acid sequences of eleven different a-amylases.Appl Microbiol Biotechnol 23: 355–360

    CAS  Google Scholar 

  • Nieto JJ, Vargas C, Ventosa A (2000) Osmoprotection mechanisms in the moderately halophilic bacterium Halomonas elongata. Rec Res Dev Microbiol 4: 43–54

    Google Scholar 

  • Onishi H (1972a) Halophilic amylase from a moderately halophilic Micrococcus. J Bacte-

    Google Scholar 

  • riol 109:570–574

    Google Scholar 

  • Onishi H (1972b) Salt response of amylase produced in media of different NaCl or KCl concentrations by a moderately halophilic Micrococcus. Can J Microbiol 18: 1617–1620

    Article  PubMed  CAS  Google Scholar 

  • Onishi H, Hidaka O (1978) Purification and properties of amylase produced by a moderately halophilic Acinetobacter sp. Can J Microbiol 24: 1017–1023

    Article  PubMed  CAS  Google Scholar 

  • Onishi H, Kamekura M (1972) Micrococcus halobius sp. nov. Int J Syst Bacteriol 22: 233–236

    Google Scholar 

  • Onishi H, Mori T, Takeuchi S, Tani K, Kobayashi T, Kamekura M (1983) Halophilic nuclease of a moderately halophilic Bacillus sp.: production, purification, and characterization. Appl Environ Microbiol 45: 24–30

    PubMed  CAS  Google Scholar 

  • Oren A (1994) Enzyme diversity in halophilic archaea. Microbiologia 10:217–228 Rodríguez-Valera F (1993) Introduction to saline environments. In: Vreeland RH, Hochstein LI (eds) The biology of halophilic bacteria. CRC Press, Boca Raton, pp 1–23

    Google Scholar 

  • Sánchez-Porro C, Martín S, Mellado E, Ventosa A (2003a) Diversity of moderately halophilic bacteria producing extracellular hydrolytic enzymes. J Appl Microbiol 94: 295–300

    Article  PubMed  Google Scholar 

  • Sánchez-Porro C, Mellado E, Bertoldo C, Antranikian G, Ventosa A (2003b) Screening and characterization of the protease CP1 produced by the moderately halophilic bacterium Pseudoalteromonas sp. strain CP76. Extremophiles 7: 221–228

    PubMed  Google Scholar 

  • Stackebrandt E, Koch C, Gvozdiak O, Schumann P (1995) Taxonomic dissection of the genus Micrococcus: Kocuria gen. nov., Nesterenkonia gen. nov., Kytococcus gen. nov., Dermacoccus gen. nov., and Micrococcus Cohn 1872 gen. emend. Int J Syst Bacteriol 45: 682–692

    Article  PubMed  CAS  Google Scholar 

  • Van Qua D, Simidu U, Taga N (198 1) Purification and some properties of halophilic protease produced by a moderately halophilic marine Pseudomonas sp. Can J Microbiol 27: 505–510

    Google Scholar 

  • Ventosa A, Nieto JJ (1995) Biotechnological applications and potentialities of halophilic microorganisms. Word J Microbiol Biotechnol 11: 85–94

    Article  CAS  Google Scholar 

  • Ventosa A, García MT, Kamekura M, Onishi H, Ruiz-Berraquero F (1989) Bacillus halophilus sp. nov., a moderately halophilic Bacillus species. Syst Appl Microbiol 12: 162–166

    Google Scholar 

  • Ventosa A, Nieto JJ, Oren A (1998) Biology of moderately halophilic aerobic bacteria. Microbiol Mol Biol Rev 62: 504–544

    PubMed  CAS  Google Scholar 

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Mellado, E., Sánchez-Porro, C., Martín, S., Ventosa, A. (2004). Extracellular Hydrolytic Enzymes Produced by Moderately Halophilic Bacteria. In: Ventosa, A. (eds) Halophilic Microorganisms. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-07656-9_21

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  • DOI: https://doi.org/10.1007/978-3-662-07656-9_21

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-05664-2

  • Online ISBN: 978-3-662-07656-9

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