Biosynthesis of Enduracidin: Origin of Enduracididine and Other Amino Acids
スポンサーリンク
概要
- 論文の詳細を見る
The biosynthetic origin of the amino acid moieties of enduracidin was investigated by feeding experiments with labeled compounds. Results of the incorporation and the distribution of radioactivity into the antibiotic revealed that glycine, L-serine, L-threonine, L-alanine, L-aspartic acid, L-ornithine and L-citrulline were incorporated into the corresponding amino acid moieties. Unique amino acids, enduracididine and its isomer with an imidazolidine ring, were derived from larginine, but not histidine. K1 (4-hydroxyphenylglycine) and K2 (3, 5-dichloro-K1) moieties were derived from L-tyrosine. 36Cl-Sodium chloride was incorporated into the antibiotic in the early stage of fermentation.
- 社団法人 日本農芸化学会の論文
著者
-
NOGAMI Ikuo
Applied Microbiology Laboratories, Central Research Division, Takeda Chemical Industries, Ltd.
-
NOGAMI Ikuo
Applied Microbiology Laboratories, Central Research Division, Takeda Chemical Industries
-
HATANO Kazunori
Applied Microbiology Laboratories, Central Research Division, Takeda Chemical Industries, Ltd.
-
HIGASHIDE Eiji
Applied Microbiology Laboratories, Central Research Division, Takeda Chemical Industries, Ltd.
-
KISHI Toyokazu
Applied Microbiology Laboratories, Central Research Division, Takeda Chemical Industries, Ltd.
関連論文
- Accumulation of Diphosphorylated Butirosin A Derivatives by Phosphatase-negative Mutants of Bacillus vitellinus
- Biosynthesis of Enduracidin: Origin of Enduracididine and Other Amino Acids
- 2-N-Acetylation of Butirosin A by Mutants of Streptomyces fradiae
- Two Alkaline Phosphatases from a Butirosin A Producer Bacillus vitellinus
- Biosynthetic Origin of the Ansa-Structure of Ansamitocin P-3
- Selective Accumulation of ansamitocins P-2, P-3 and P-4, and Biosynthetic Origins of Their Acyl Moieties
- Biosynthesis of Macbecin
- Bioassay of Ansamitocin P-3, an Antitumor Antibiotic