Structural gene and complete amino acid sequence of Vibrio alginolyticus collagenase

Author:

Takeuchi H1,Shibano Y2,Morihara K3,Fukushima J1,Inami S1,Keil B4,Gilles A M4,Kawamoto S1,Okuda K1

Affiliation:

1. Department of Bacteriology, Yokohama City University School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama 236, Osaka

2. Laboratory of Applied Microbiology, Suntory Limited Research Center, Shimamoto-Cho, Mishima-Gun, Osaka

3. Institute for Applied Life Science and Department of Enzymology, University of East Asia, 2-1 Ichinomiya-Gakuencho, Shimonoseki-Shi, Yamaguchi 751, Japan

4. Institut Pasteur, 28 rue du Docteur Roux, 75724 Paris Cédex 15, France

Abstract

The DNA encoding the collagenase of Vibrio alginolyticus was cloned, and its complete nucleotide sequence was determined. When the cloned gene was ligated to pUC18, the Escherichia coli expression vector, bacteria carrying the gene exhibited both collagenase antigen and collagenase activity. The open reading frame from the ATG initiation codon was 2442 bp in length for the collagenase structural gene. The amino acid sequence, deduced from the nucleotide sequence, revealed that the mature collagenase consists of 739 amino acids with an Mr of 81875. The amino acid sequences of 20 polypeptide fragments were completely identical with the deduced amino acid sequences of the collagenase gene. The amino acid composition predicted from the DNA sequence was similar to the chemically determined composition of purified collagenase reported previously. The analyses of both the DNA and amino acid sequences of the collagenase gene were rigorously performed, but we could not detect any significant sequence similarity to other collagenases.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

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