Effect of pre-fermentation on the production of cutinase by a recombinant Saccharomyces cerevisiae

The importance of controlling the expression of heterologous cutinase in a recombinant Saccharomyces cerevisiae SU50 strain was investigated. Maximum specific growth rate and the biomass yield increased 1.91 and 1.16 fold, respectively, when cutinase production was induced by galactose in a pre-ferm...

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Veröffentlicht in:Journal of bioscience and bioengineering 2002-04, Vol.93 (4), p.354-359
Hauptverfasser: Calado, Cecília R.C., Monteiro, Sandra M.S., Cabral, Joaquim M.S., Fonseca, Luis P.
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container_issue 4
container_start_page 354
container_title Journal of bioscience and bioengineering
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creator Calado, Cecília R.C.
Monteiro, Sandra M.S.
Cabral, Joaquim M.S.
Fonseca, Luis P.
description The importance of controlling the expression of heterologous cutinase in a recombinant Saccharomyces cerevisiae SU50 strain was investigated. Maximum specific growth rate and the biomass yield increased 1.91 and 1.16 fold, respectively, when cutinase production was induced by galactose in a pre-fermentation step. However, only 19% of specific cell activity was obtained in comparison to other fermentations following a pre-fermentation step without induction of cutinase expression. Thus, the pre-fermentation step was performed using a selective medium not containing galactose, and the fermentation was performed with a cheaper and complex non-selective medium containing galactose. Under these conditions, and with the aim of maximising the specific cutinase activity, a pre-fermentation with low volume and high density of viable cells must be used. However, due to the low pre-fermentation volume, low yeast cell concentrations and low specific cell activities were obtained after 96 h of fermentation. Otherwise, when the aim was to maximise cutinase yield and productivity, a pre-fermentation volume of 10% (v/v) in relation to fermentation and in the exponential growth phase with a cell concentration between 1.1 and 1.8 g dcw/ l should be used. A higher pre-fermentation volume, such as 20% (v/v), would still be economical in the case of a pre-fermentation with low cell density or low cell viability.
doi_str_mv 10.1016/S1389-1723(02)80067-6
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Otherwise, when the aim was to maximise cutinase yield and productivity, a pre-fermentation volume of 10% (v/v) in relation to fermentation and in the exponential growth phase with a cell concentration between 1.1 and 1.8 g dcw/ l should be used. A higher pre-fermentation volume, such as 20% (v/v), would still be economical in the case of a pre-fermentation with low cell density or low cell viability.</description><identifier>ISSN: 1389-1723</identifier><identifier>EISSN: 1347-4421</identifier><identifier>DOI: 10.1016/S1389-1723(02)80067-6</identifier><identifier>PMID: 16233214</identifier><identifier>CODEN: JFBIEX</identifier><language>eng</language><publisher>Amsterdarm: Elsevier B.V</publisher><subject>Biological and medical sciences ; Biotechnology ; cutinase ; Enzyme engineering ; FERMENTATION ; Fundamental and applied biological sciences. Psychology ; FUSARIUM SOLANI ; Fusarium solani pisi ; GALACTOSE ; HYDROLASES ; inoculum ; Methods. Procedures. 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source ScienceDirect Journals (5 years ago - present)
subjects Biological and medical sciences
Biotechnology
cutinase
Enzyme engineering
FERMENTATION
Fundamental and applied biological sciences. Psychology
FUSARIUM SOLANI
Fusarium solani pisi
GALACTOSE
HYDROLASES
inoculum
Methods. Procedures. Technologies
pre-fermentation
Production of selected enzymes
RECOMBINANT DNA
SACCHAROMYCES CEREVISIAE
title Effect of pre-fermentation on the production of cutinase by a recombinant Saccharomyces cerevisiae
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