Identification and Characterization of Acetyl-CoA Carboxylase Gene Cluster in Streptomyces toxytricini

被引:13
|
作者
Demirev, Atanas V. [3 ]
Lee, Ji Seon [1 ]
Sedai, Bhishma R. [1 ]
Ivanov, Ivan G. [2 ]
Nam, Doo Hyun [1 ]
机构
[1] Yeungnam Univ, Fac Pharm, Gyongsan 712749, South Korea
[2] Bulgarian Acad Sci, Inst Mol Biol, Dept Gene Regulat, BU-1113 Sofia, Bulgaria
[3] Yeungnam Univ, Fac Biotechnol, Gyongsan 712749, South Korea
关键词
acetyl-CoA carboxylase; biotin carboxylase; carboxyltransferase; biotin apo-protein ligase; Streptomyces toxytricini; LIPASE INHIBITOR LIPSTATIN; COENZYME-A CARBOXYLASE; BIOTIN PROTEIN LIGASE; ESCHERICHIA-COLI; MYCOBACTERIUM-TUBERCULOSIS; BIOSYNTHETIC ORIGIN; PANCREATIC LIPASE; COELICOLOR A3(2); CLONING; SPECIFICITY;
D O I
10.1007/s12275-009-0135-5
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The gene locus for acetyl-CoA carboxylase (ACC) involved in the primary metabolism was identified from the genomic library or Streptomyces toxytricini which produces a lipase inhibitor lipstatin. The 7.4 kb cloned gene was comprised of 5 ORFs including accD1, accA1, hmgL, fadST1, and stsF. In order to confirm the biochemical characteristics of AccA1, the gene was overexpressed in Escherichia coli cells, and the recombinant protein was purified through Ni2+ affinity chromatography. Because most of the expressed AccA1 was biotinylated by host E. coli BirA in the presence of D-biotin, the non-biotinylated apo-AccA1 was purified after gene induction without D-biotin, followed by exclusion of holo-AccA1 using streptavidin beads. The separated apo-AccA1 was post-translationally biotinylated by S. toxytricini biotin apo-protein ligase (BPL) in a time- and enzyme-dependent manner. This result supports that this gene cluster of S. toxytricini encodes the functional ACC enzyme subunits to be biotinylated.
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页码:473 / 478
页数:6
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