Genetic engineering of Trichoderma to produce strains with novel cellulase profiles.

Abstract:

:Genetic engineering has been used to modify the proportion of different cellulases produced by a hypercellulolytic Trichoderma reesei mutant strain. A general expression vector, pAMH110, containing the promoter and terminator sequences of the strongly expressed main cellobiohydrolase 1 (cbh1) gene was used to overexpress a cDNA coding for EGI, the major endoglucanase (1,4,beta-D-glucan glucanohydrolase, EC 3.2.1.4). An in vitro modified cbh1 cDNA, incapable of coding for active enzyme, was used to inactivate the major cellobiohydrolase (1,4-beta-D-glucan cellobiohydrolase, EC 3.2.1.91) gene. In this way, new strains producing elevated amounts of the specific endoglucanase 1 (EGI) and/or lacking the major cellobiohydrolase (CBHI) were produced, and these have been further characterized.

journal_name

Enzyme Microb Technol

authors

Harkki A,Mäntylä A,Penttilä M,Muttilainen S,Bühler R,Suominen P,Knowles J,Nevalainen H

doi

10.1016/0141-0229(91)90133-u

keywords:

subject

Has Abstract

pub_date

1991-03-01 00:00:00

pages

227-33

issue

3

eissn

0141-0229

issn

1879-0909

pii

0141-0229(91)90133-U

journal_volume

13

pub_type

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