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中国生物工程杂志

China Biotechnology
China Biotechnology  2008, Vol. 28 Issue (12): 77-81    DOI:
    
Primary Study of Producing UMP by Overexpressing URA5 and URA3 Genes in Saccharomyces cerevisiae
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Abstract  

To increase the biotransfomation efficiency from the orotic acid to the Uridine 5’-monophosphate(UMP), URA5 gene encoding Orotate phosphoribosytransferase was amplified from Saccharomyces cerevisiae BY4742 by PCR, then it was inserted into the expression vector pYX212(contained orotidine monophosphate decarboxylase gene URA3)and the pYX212-URA5 was transformed into Saccharomyces cerevisiae BJX12 by electroporation. The recombinant strain was elementarily used to convert orotic acid to UMP. The results showed that pYX212-URA5/BJX12 could accumulate 7mM UMP from 32mM orotic acid in 26h, significantly higher than both control groups pYX212/BJX12 ( 2.7mM ) and BJX12 ( 2.4 mM )



Key wordsBiocatalysis      Uridine 5’-monophosphate(UMP)      Orotate phosphoribosytransferase(OPRTase)      orotidine monophosphate decarboxylase(ODCase)      Saccharomyces cerevisiae     
Received: 25 July 2008      Published: 20 April 2009
Cite this article:

. Primary Study of Producing UMP by Overexpressing URA5 and URA3 Genes in Saccharomyces cerevisiae. China Biotechnology, 2008, 28(12): 77-81.

URL:

https://manu60.magtech.com.cn/biotech/     OR     https://manu60.magtech.com.cn/biotech/Y2008/V28/I12/77

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