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[Cloning, expression and sequence analysis of DS I gene in Corynebacterium pekinense AS1.299 and PD-67]
Chunhua Zhang1, Zhi Zhao, Yingzi Zhang
1Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
Objective:
3-deoxy-D-arabinoheptulosonate-7-phosphate synthase (EC 2.5.1.54;DS) is the key enzyme in tryptophan synthesis pathway. Cloning DS I gene from Corynebacterium pekinense and expression of DS I gene might facilitate testing the existence and function of DS I in Corynebacterium pekinense.
Methods:
According to the homology between Corynebacterium glutamicum ATCC13032 and Corynebacterium pekinense, we designed a pair of PCR primers to clone the DS I gene from wild-type C. pekinense AS1.299 and its mutant PD-67, then the mutant DS I gene was expressed in C. pekinense PD-67 by subcloning the the PCR fragment into plasmid pAK6.
Results:
Analysis of PCR fragments revealed that they contained the whole DS I gene. There was no base change all over the structure genes and regulatory sequences between C. pekinense AS1.299 and PD-67. An internal promoter was found in the upstream of the DS I gene from C. pekinense and it functioned in E. coli 3257. The DS I gene from C. pekinense PD-67 was expressed homogenously, and the specific enzyme activity of DS I in C. pekinense PD-67 (pAD1) was much higher than that of the control strain C. pekinense PD-67(pAK6).
Conclusion:
This is the first report that DS I gene existed in Corynebaterium Pekinense, The amplification of the specific activity of DS I is expected to increase L-tryptophan accumulation of C. pekinense PD-67.
