Cloning, expression, and characterization of an adenylate cyclase from Arthrobacter sp CGMCC 3584

被引:12
作者
He, Ying [1 ]
Li, Nan [1 ]
Chen, Yong [1 ]
Chen, Xiaochun [1 ]
Bai, Jianxin [1 ]
Wu, Jinglan [1 ]
Xie, Jingjing [1 ]
Ying, Hanjie [1 ]
机构
[1] Nanjing Univ Technol, State Key Lab Mat Oriented Chem Engn, Coll Life Sci & Pharmaceut Engn, Nanjing 210009, Peoples R China
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
Adenylate cyclase; Arthrobacter; Cyclic adenosine monophosphate; Expression; Characterization; BORDETELLA-PERTUSSIS; PURIFICATION; CALMODULIN; AMPLIFICATION; CATALYSIS; PROTEIN; ATP;
D O I
10.1007/s00253-012-3890-x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The cya gene encoding adenylate cyclase was cloned from Arthrobacter sp. CGMCC 3584 by thermal asymmetric interlaced PCR for the first time. It exhibited an open reading frame containing 1,125 bp and encoding 374 amino acids. Amino acid sequence analysis showed that this enzyme was a class III adenylate cyclase. Expression of the cya gene was carried out in Escherichia coli Rosetta, and purification was performed via Ni2+-NTA agarose gel column. SDS-PAGE indicated that the molecular mass of the recombinant adenylate cyclase was 45 kDa. The V (max) and K (m) were determined to be 5.06 mu mol/min/mg and 7.56 mM, respectively. The optimum pH and temperature were 8.0 and 35 A degrees C. Several divalent metal ions were found to activate the enzyme to different extents, and the maximal specific activity reached 3.04 mu mol/min/mg when 50 mM Mg2+ was added. This was the first report of the cloning of an adenylate cyclase gene from Arthrobacter sp.
引用
收藏
页码:963 / 970
页数:8
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