4.4 Article

Genetic and Biochemical Characterization of the Pseudoalteromonas tetraodonis Alkaline κ-Carrageenase

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BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
卷 76, 期 3, 页码 506-511

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TAYLOR & FRANCIS LTD
DOI: 10.1271/bbb.110809

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carrageenase; deep sea; Pseudoalteromonas; alkaline enzyme

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An alkaline K-carrageenase, Cgk-K142, was found in the culture broth of a deep-sea bacterium, Pseudoalteromonas tetraodonis JAM-K142. A gene for the enzyme was cloned and expressed. Purified recombinant Cgk-K142 (rCgk-K142) showed an optimal pH of about 8.8 in glycine-NaOH buffer at 30 degrees C and of about 8.0 in MOPS buffer at 50 degrees C. The optimal temperature for the enzyme was 55 degrees C at pH 8.0. rCgk-K142 was unstable, but lambda- and iota-carrageenans, non-degradative substrate homologs, extensively enhanced its stability. The nucleotide sequence of the gene for Cgk-K142 comprised 1,194 bp, and the deduced amino acid sequence (397 amino acids) showed a high level of similarity to the kappa-carrageenase of P. carrageenovora, with 94% identity. Another gene for a kappa-carrageenase-like protein was found downstream of the gene for Cgk-K142. The nucleotide sequence of that gene consisted of 966 bp (321 amino acids), and it showed the highest similarity, at 64% identity, to protein CgkB of P. carrageenovora, which has been reported as an incomplete 57-amino acid sequence.

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