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Identification and characterization of a novel citrate synthase from Streptomyces diastaticus No. 7 strain M1033
Author(s) -
Ge Yadong,
Cao Zhengyu,
Song Ping,
Zhu Guoping
Publication year - 2015
Publication title -
biotechnology and applied biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.468
H-Index - 70
eISSN - 1470-8744
pISSN - 0885-4513
DOI - 10.1002/bab.1372
Subject(s) - citrate synthase , enzyme , citric acid cycle , chemistry , tricarboxylic acid , molecular mass , biochemistry , bacteria , mass spectrometry , peptide sequence , streptomyces , streptomycetaceae , actinomycetales , size exclusion chromatography , enzyme kinetics , atp synthase , chromatography , strain (injury) , biology , active site , anatomy , gene , genetics
Abstract Citrate synthase (CS) is a key enzyme of the tricarboxylic acid cycle and is widely distributed among prokaryotes and eukaryotes. Here, we report for the first time, the cloning, expression, and characterization of a novel CS from Streptomyces diastaticus No. 7 strain M1033 ( Sd CS). Gel filtration chromatography and matrix‐assisted laser‐desorption ionization–time‐of‐flight mass spectrometry (MALDI‐TOF‐MS) analyses indicate that Sd CS forms homodimers with a molecular mass of approximately 100.0 kDa. The predicted amino acid sequence of Sd CS is highly similar to those of bacterial homodimeric type I CSs. The pH and temperature optima for Sd CS activity were 8.0 and 35 °C, respectively. The half‐life ( t 1/2 ) of Sd CS was 10 Min at 50 °C and was increased to 210 Min in the presence of oxaloacetate. The kinetic parameters of Sd CS ( k cat = 262.8 and 230.7 s −1 ; K m = 58.4 and 11.2 µM for acetyl‐CoA and oxaloacetate, respectively) were comparable to those of dimeric CSs isolated from Gram‐positive bacteria and eukaryotes. Moreover, Sd CS activity was inhibited by ATP and ADP and stimulated by AMP. These findings provide a foundation for further investigations on the three‐dimensional structure and mechanism of catalysis of Sd CS.