4.4 Article

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

Journal

JOURNAL OF MICROBIOLOGY
Volume 47, Issue 4, Pages 473-478

Publisher

MICROBIOLOGICAL SOCIETY KOREA
DOI: 10.1007/s12275-009-0135-5

Keywords

acetyl-CoA carboxylase; biotin carboxylase; carboxyltransferase; biotin apo-protein ligase; Streptomyces toxytricini

Categories

Funding

  1. Korea Research Fund [KRF-2006-311-E00582]
  2. National Research Foundation of Korea [2006-311-E00582] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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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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