4.7 Article

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

期刊

APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
卷 96, 期 4, 页码 963-970

出版社

SPRINGER
DOI: 10.1007/s00253-012-3890-x

关键词

Adenylate cyclase; Arthrobacter; Cyclic adenosine monophosphate; Expression; Characterization

资金

  1. National Science Fund for Distinguished Young Scholars [21025625]
  2. National Basic Research Program of China (973) [2011CBA00806]
  3. Research Fund for the Doctoral Program of Higher Education of China [20113221120007]
  4. Program for New Century Excellent Talents in University of Ministry of Education of China
  5. National Natural Science Foundation of China [21106070]
  6. program for Changjiang Scholars and Innovative Research Team in University
  7. Priority Academic Program from Development of Jiangsu Higher Education Institutions

向作者/读者索取更多资源

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.

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