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中国生物工程杂志

China Biotechnology
China Biotechnology  2008, Vol. 28 Issue (5): 46-51    DOI:
    
Construction of dhaBCE and yqhD co-expression vector and its biotransformation of glycerol
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Abstract  

DhaBCE from Klebsiella.pneumoniae was inserted into the yqhD upriver in the plasmid pET28(a+)-yqhD. The recombinant plasmid pET28(a+)dhaBCE-yqhD harboring the genes encoding dhaBCE and yqhD with a Shine-Dalgarno (SD) sequence was transformed into E. coli novablue to be co-expression. The results showed that after 16 hours calculated following the addition of inducer IPTG at induce temperature 28℃, the enzyme activity of glycerol dehydratase and yqhD. oxidoreductase in recombined strain could arrive 35 U/ mg and 82 U/ mg, individually, higher than the wild type. The yield of 1, 3-PD arrived at 39g/L when 55g/L of substrate glycerol was added in the fermentation culture. Excessive glycerol badly influence produce formation and inhibition of product on 1, 3-propenediol biotransformation existed.



Key wordsglycerol dehydratase      yqhD oxidoresuctase      co-expression      1      3-propenediol     
Received: 25 December 2007      Published: 25 May 2008
Cite this article:

. Construction of dhaBCE and yqhD co-expression vector and its biotransformation of glycerol. China Biotechnology, 2008, 28(5): 46-51.

URL:

https://manu60.magtech.com.cn/biotech/     OR     https://manu60.magtech.com.cn/biotech/Y2008/V28/I5/46

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