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PMID: 1368665 Published · ppublish English Journal Article

Xylose (glucose) isomerase gene from the thermophile Clostridium thermohydrosulfuricum; cloning, sequencing, and expression in Escherichia coli.

Agricultural and biological chemistry ·Vol. 55 ·No. 1 ·1991-01-00 ·Pages 221-7

Dekker K, Yamagata H, Sakaguchi K, Udaka S

Abstract

The xylose isomerase gene from the thermophile Clostridium thermohydrosulfuricum has been cloned, using a fragment of the Bacillus subtilis gene as a probe. The complete nucleotide sequence of the gene was analyzed. C. thermohydrosulfuricum is the most thermophilic organism from which a xylose isomerase gene has been cloned and characterized. Comparison with amino acid sequences from other xylose isomerases showed that amino acids involved in substrate binding and isomerization are well conserved. Purification of the enzyme produced in E. coli was done by heating a cell-free extract at 85 degrees C for 10 min, giving a 20-fold purified enzyme. The native enzyme is a homomeric tetramer with a molecular weight of 200,000.

MeSH Terms
Aldose-Ketose Isomerases Amino Acid Sequence Base Sequence Binding Sites Carbohydrate Epimerases/biosynthesis,genetics Cloning, Molecular Clostridium/enzymology,genetics Escherichia coli/genetics Gene Expression Molecular Sequence Data Molecular Structure Plasmids/genetics Protein Engineering Recombinant Proteins/biosynthesis Sequence Homology, Nucleic Acid
Chemicals
Recombinant Proteins Carbohydrate Epimerases Aldose-Ketose Isomerases xylose isomerase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Dekker K
Faculty of Agriculture, Nagoya University, Japan.
Yamagata H
Sakaguchi K
Udaka S
Article Info
Journal
Agricultural and biological chemistry
Abbr.
Agric Biol Chem
ISSN
0002-1369
Published
1991-01-00
Pages
221-7
Language
English
Region
Japan
NLM ID
0370452
External Links
PubMed source
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