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The Glucose Kinase of Bacillus subtilis

The Glucose Kinase of Bacillus subtilis The Glucose Kinase of Bacillus subtilis Pierre Skarlatos and Michael K. Dahl * Lehrstuhl für Mikrobiologie, Institut für Mikrobiologie, Biochemie und Genetik, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058 Erlangen, Germany ABSTRACT The open reading frame yqgR (now termed glcK ), which had been sequenced as part of the genome project, encodes a glucose kinase of Bacillus subtilis . A 1.1-kb DNA fragment containing glcK complemented an Escherichia coli strain deficient in glucose kinase activity. Insertional mutagenesis of glcK resulted in a complete inactivation of glucose kinase activity in crude protein extracts, indicating that B. subtilis contains one major glucose kinase. The glcK gene encodes a 321-residue protein with a molecular mass of 33.5 kDa. The glucose kinase was overexpressed as a fusion protein to a six-His affinity tag and purified to homogeneity. The enzyme had K m values for ATP and glucose of 0.77 and 0.24 mM, respectively, and a V max of 93 μmol min −1 mg −1 . A B. subtilis strain deficient for glucose kinase grew at the same rate on different carbon sources tested, including disaccharides such as maltose, trehalose, and sucrose. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Journal of Bacteriology American Society For Microbiology

The Glucose Kinase of Bacillus subtilis

Journal of Bacteriology , Volume 180 (12): 3222 – Jun 15, 1998

The Glucose Kinase of Bacillus subtilis

Journal of Bacteriology , Volume 180 (12): 3222 – Jun 15, 1998

Abstract

The Glucose Kinase of Bacillus subtilis Pierre Skarlatos and Michael K. Dahl * Lehrstuhl für Mikrobiologie, Institut für Mikrobiologie, Biochemie und Genetik, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058 Erlangen, Germany ABSTRACT The open reading frame yqgR (now termed glcK ), which had been sequenced as part of the genome project, encodes a glucose kinase of Bacillus subtilis . A 1.1-kb DNA fragment containing glcK complemented an Escherichia coli strain deficient in glucose kinase activity. Insertional mutagenesis of glcK resulted in a complete inactivation of glucose kinase activity in crude protein extracts, indicating that B. subtilis contains one major glucose kinase. The glcK gene encodes a 321-residue protein with a molecular mass of 33.5 kDa. The glucose kinase was overexpressed as a fusion protein to a six-His affinity tag and purified to homogeneity. The enzyme had K m values for ATP and glucose of 0.77 and 0.24 mM, respectively, and a V max of 93 μmol min −1 mg −1 . A B. subtilis strain deficient for glucose kinase grew at the same rate on different carbon sources tested, including disaccharides such as maltose, trehalose, and sucrose.

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Publisher
American Society For Microbiology
Copyright
Copyright © 1998 by the American society for Microbiology.
ISSN
0021-9193
eISSN
1098-5530
Publisher site
See Article on Publisher Site

Abstract

The Glucose Kinase of Bacillus subtilis Pierre Skarlatos and Michael K. Dahl * Lehrstuhl für Mikrobiologie, Institut für Mikrobiologie, Biochemie und Genetik, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058 Erlangen, Germany ABSTRACT The open reading frame yqgR (now termed glcK ), which had been sequenced as part of the genome project, encodes a glucose kinase of Bacillus subtilis . A 1.1-kb DNA fragment containing glcK complemented an Escherichia coli strain deficient in glucose kinase activity. Insertional mutagenesis of glcK resulted in a complete inactivation of glucose kinase activity in crude protein extracts, indicating that B. subtilis contains one major glucose kinase. The glcK gene encodes a 321-residue protein with a molecular mass of 33.5 kDa. The glucose kinase was overexpressed as a fusion protein to a six-His affinity tag and purified to homogeneity. The enzyme had K m values for ATP and glucose of 0.77 and 0.24 mM, respectively, and a V max of 93 μmol min −1 mg −1 . A B. subtilis strain deficient for glucose kinase grew at the same rate on different carbon sources tested, including disaccharides such as maltose, trehalose, and sucrose.

Journal

Journal of BacteriologyAmerican Society For Microbiology

Published: Jun 15, 1998

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