| 研究报告 |
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| Cloning, sequence analysis and expression of dhaT gene from Citrobacter freundii and purification and property of corresponding recombinant enzyme |
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Abstract 1,3-propanediol (1,3-PD) is an important material for chemical industry, therefore, there is much interest in the production of 1,3-PD. The gene dhaT encoding 1, 3-propanediol dehydrogenase (PDOR) of Citrobacter freundii was amplified by PCR. Sequence analysis of the similarity at the nucleotide and amino acid level between the gene encoding C. freundii PDOR and that of C.freundii (U09771) were 78% and 90%, respectively. The recombinant plasmid pSE-dhaT was constructed by inserting dhaT gene into expression vector pSE380 and then transformed E. coli JM109. The recombinant strain was induced by IPTG to express dhaT. Further more the recombinant enzyme was purifed from recombinant E.coli by Ni-nitrilotriacetate affinity chromatography followed by Sephacral S-300 gel filtration. A single obvious protein about 42kDa could be obtained by the sodium dodecyl sulfate-polyacrylamide gel electrophoresis of recombinant enzyme. The purified enzyme was used to determined enzyme property on the substrate of propionaldehyde and 1, 3-PD. The optimal temperature and optimal pH of the purified enzyme were 37℃, 8.0 for reduction and 25℃, 10.5 for oxidation, respectively; and the kinetic property of PDOR about Km and Vmax were 10.05mmol/L, 37.27umol/min/mg for propionaldehyde and 1.28mmol/L, 25.55umol/min/mg for 1,3-PD, respectively; The deduced dhaT gene product (388 amino acids) showed a specific reduction activity of 49.50U/mg and oxidation activity of 79.92U/mg. There also have a putative iron-binding motif (G-XX-H-X-X-A-H-X-X-G-X-X-X-X-X-P-H-G) as a fingerprint pattern in our recombinant enzyme, the motif is fully conserved among these 1,3-propanediol dehydrogenase. This study is beneficial to the researches of high producing 1, 3-propanediol by gene engineering strain.
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Received: 24 February 2006
Published: 25 July 2006
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