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中国生物工程杂志

China Biotechnology
China Biotechnology  2012, Vol. 32 Issue (02): 29-32    DOI:
    
Cloning and Expression of S-mandelate Dehydrogenase Gene
ZENG Zhen, YANG Jun-fang, YANG Cheng-li, WANG Peng, LI Da-li
Department of Bioengineering, Nanjing University of Science and Technology, Nanjing 210094, China
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Abstract  

S-mandelate dehydrogenase(SMDH) can catalyze S-mandelic acid to benzoylformic acid. The SMDH nucleotide gene(mdlA)was cloned from DNA of Pseudomonas putida NUST by PCR, and the amplicon was inserted into prokaryotic expression vector pET-30a (+). This recombinant was transformed into E. coli BL21(DE3) and then highly expressed by induction of IPTG. The result of SDS-PAGE showed that the molecular weight of cloned SMDH was about 43kDa. The recombinant strain could catalyze S-mandelate to benzoylformic acid.



Key wordsBiocatalyst      S-Mandelate dehydrogenase      Cloning      Expression     
Received: 31 October 2011      Published: 25 February 2012
ZTFLH:  Q819  
Cite this article:

ZENG Zhen, YANG Jun-fang, YANG Cheng-li, WANG Peng, LI Da-li. Cloning and Expression of S-mandelate Dehydrogenase Gene. China Biotechnology, 2012, 32(02): 29-32.

URL:

https://manu60.magtech.com.cn/biotech/     OR     https://manu60.magtech.com.cn/biotech/Y2012/V32/I02/29


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