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KMID : 0545120040140030563
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Journal of Microbiology and Biotechnology
2004 Volume.14 No. 3 p.563 ~ p.569
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Cloning and Expression of a Novel Chitosanase Gene (choK) from β-Proteobacterium KNU3 by Double Inverse PCR
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Yi JH
Lee KE/Choi SG
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Abstract
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The DNA sequence of the chitosanase gene (choK) from b-Proteobacterium KNU3 showed an 1158-bp open reading frame that encodes a protein of 386 amino acids with a novel 74 signal peptide. The degenerated primers based on the partial deduced amino acid sequences from MALDI-TOF MS analyses yielded the 820 bp of the PCR product. Based on this information double inverse PCR cloning experiments which use the two specific sets of PCR primers rather than single set primers identified the unknown 1.2 kb of the choK gene. Subsequently a 1.8 kb of full choK gene was cloned from another PCR cloning experiment and it was then subcloned into pGEM T-easy and pUC18 vectors. The recombinant E. coli clone harboring recombinant pUC18 vector produced a clear halo around the colony in the glycol chitosan plates. The recombinant ChoK protein was secreted into medium in a mature form while the intracellular ChoK was produced without signal peptide cleavage. The activity staining of PAGE showed that the recombinant ChoK protein was identical to the chitosanase of wildtype. The comparison of deduced amino acid sequences of choK revealed that there is 92% identity with that of Sphingobacterium multivorum chitosanase. Judging from the conserved module in other bacterial chitosanases chitosanase of KNU3 strain (ChoK) belongs to the family 80 of glycoside hydrolases.
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