Abstract
Chitinase production in Streptomyces lividans is induced by chitin and repressed in the presence of glucose. A mutant of S. lividans TK24, strain G015, which was defective in glucose repression of chitinase production, was obtained by screening colonies for zones of clearing on colloidal chitin agar plates containing 1.0% (wt/vol) glucose. The transcriptional analysis of chiA in G015 with xylE, which encodes catechol 2,3-dioxygenase, as a reporter gene showed that the transcription from the chiA promoter of S. lividans TK24 occurred regardless of the presence of glucose. G015 was resistant to 2-deoxyglucose (2-DOG) and did not utilize glucose as a sole carbon source. When a DNA fragment containing glkA, a gene for glucose kinase, of Streptomyces coelicolor A3(2) was introduced into strain G015 on a low-copy-number plasmid, the sensitivity to 2-DOG, the ability to utilize glucose, and the glucose repression of chitinase production were restored. These results indicate that glkA is involved in glucose repression of chitinase production in S. lividans TK24.
MeSH Terms
Bacterial Proteins/genetics,physiology
Catechol 2,3-Dioxygenase
Chitin/pharmacology
Chitinases/biosynthesis,genetics
Deoxyglucose/pharmacology
Dioxygenases
Enzyme Repression
Gene Expression Regulation, Bacterial
Glucokinase/genetics,physiology
Glucose/metabolism,pharmacology
Oxygenases/genetics
Promoter Regions, Genetic/genetics
Recombinant Fusion Proteins
Streptomyces/enzymology,genetics
Chemicals
Bacterial Proteins
Recombinant Fusion Proteins
Chitin
Deoxyglucose
Oxygenases
Dioxygenases
Catechol 2,3-Dioxygenase
GlkA protein, Bacteria
Glucokinase
Chitinases
chitinase ChiA
Glucose
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Saito A
National Institute of Agro-Environmental Sciences, 3-1-1 Kan-nondai, Tsukuba, Ibaraki 305-8604, Japan.
Fujii T
Yoneyama T
Miyashita K
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