Literature DB >> 18454328

Enhanced production of cellulases byCellulomonas strains grown on different cellulosic residues.

M I Rajoka1, K A Malik.   

Abstract

Cellulomonas strains consumed commercial cellulose, cellulosic residues, xylan, cellobiose and carboxymethyl cellulose (CMC) as carbon sources in liquid culture, the growth being the most on cellobiose medium. All three components of the cellulase complex ofCellulomonas were produced when the organisms utilized all substrates as sole carbon and energy sources. The filter-paper cellulase (FPase) and endo-glucanase (CMCase) activities were higher in media containing alpha-cellulose and cellulosic residues than in media containing CMC, cellobiose, and xylan. Cell-free supernatants of all organisms exhibited greater CMC hydrolyzing activity than filter paper and beta-glucoside hydrolyzing activities. All strains synthesized beta-glucosidase maximally on cellobiose followed by commercial cellulose and cellulosic residues.C. biazotea produced the highest FPase and CMCase activity during growth on alpha-cellulose. It was followed byC. flavigena, C. cellasea, andC. fimi. Endo-glucanase and FPase from all organisms were secreted into the medium; 10-13 % became adsorbed on the surface of the insoluble substrates and could be successfully eluted using Tween 80. beta-Glucosidase was located in cell extracts from all organisms.C. biazotea produced FPase and beta-glucosidase activities several-fold greater than those produced by many other strains ofCellulomonas and some other cellulolytic bacteria and fungi.

Entities:  

Year:  1997        PMID: 18454328     DOI: 10.1007/BF02898647

Source DB:  PubMed          Journal:  Folia Microbiol (Praha)        ISSN: 0015-5632            Impact factor:   2.629


  9 in total

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Journal:  Annu Rev Microbiol       Date:  1990       Impact factor: 15.500

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Authors:  W Stoppok; P Rapp; F Wagner
Journal:  Appl Environ Microbiol       Date:  1982-07       Impact factor: 4.792

4.  Regulation of beta-1,4-Endoglucanase Synthesis in Thermomonospora fusca.

Authors:  E Lin; D B Wilson
Journal:  Appl Environ Microbiol       Date:  1987-06       Impact factor: 4.792

5.  Regulation of envelope protein composition during adaptation to osmotic stress in Escherichia coli.

Authors:  A Barron; G May; E Bremer; M Villarejo
Journal:  J Bacteriol       Date:  1986-08       Impact factor: 3.490

6.  In vitro production of pectolytic and cellulolytic enzymes byColletotrichum lindemuthianum isolated from soybean grown in Saudi Arabia.

Authors:  A H Bahkali
Journal:  World J Microbiol Biotechnol       Date:  1992-01       Impact factor: 3.312

7.  Cellulase production by mixed fungi in solid-substrate fermentation of bagasse.

Authors:  R Dueñas; R P Tengerdy; M Gutierrez-Correa
Journal:  World J Microbiol Biotechnol       Date:  1995-05       Impact factor: 3.312

Review 8.  Molecular biology of xylan degradation.

Authors:  J A Thomson
Journal:  FEMS Microbiol Rev       Date:  1993-01       Impact factor: 16.408

Review 9.  The Trichoderma cellulase regulatory puzzle: from the interior life of a secretory fungus.

Authors:  C P Kubicek; R Messner; F Gruber; R L Mach; E M Kubicek-Pranz
Journal:  Enzyme Microb Technol       Date:  1993-02       Impact factor: 3.493

  9 in total
  2 in total

1.  Cloning and expression of beta-glucosidase genes in Escherichia coli and Saccharomyces cerevisiae using shuttle vector pYES 2.0.

Authors:  M I Rajoka; A Bashir; S R Hussain; M T Ghauri; S Parvez; K A Malik
Journal:  Folia Microbiol (Praha)       Date:  1998       Impact factor: 2.099

2.  Optimization of Arundo donax Saccharification by (Hemi)cellulolytic Enzymes from Pleurotus ostreatus.

Authors:  Rossana Liguori; Elena Ionata; Loredana Marcolongo; Luciana Porto de Souza Vandenberghe; Francesco La Cara; Vincenza Faraco
Journal:  Biomed Res Int       Date:  2015-11-05       Impact factor: 3.411

  2 in total

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