Tripropeptins, Novel Antimicrobial Agents Produced by Lysobacter sp. II. Structure Elucidation.
Hideki Hashizume, Sehei Hirosawa, Ryûichi Sawa, YASUHIKO MURAOKA, Daishiro Ikeda, HIROSHI NAGANAWA, Masayuki Igarashi
Abstract
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Hideki Hashizume, Sehei Hirosawa, Ryûichi Sawa, YASUHIKO MURAOKA, Daishiro Ikeda, HIROSHI NAGANAWA, Masayuki Igarashi
Abstract
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Planar structures of tripropeptins (TPPs) were elucidated by spectroscopic studies including various NMR measurements. Stereochemistry of constituent amino acids of tripropeptin C (TPPC) (3) was identified by marfey's method except hydroxyproline which was determined by studies of NMR and CD spectra. The absolute structure of 3 was determined by analyses of the fragments obtained by Birch reduction and LiBH4 reduction of 3. The configuration of the fatty acid, isolated from acid hydrolysate of 3, was determined to be (3R)-hydroxy-13-methyltetradecanoic acid from MS, NMR spectra and negative sign of the optical rotation.
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Planar structures of tripropeptins (TPPs) were elucidated by spectroscopic studies including various NMR measurements. Stereochemistry of constituent amino acids of tripropeptin C (TPPC) (3) was identified by marfey's method except hydroxyproline which was determined by studies of NMR and CD spectra. The absolute structure of 3 was determined by analyses of the fragments obtained by Birch reduction and LiBH4 reduction of 3. The configuration of the fatty acid, isolated from acid hydrolysate of 3, was determined to be (3R)-hydroxy-13-methyltetradecanoic acid from MS, NMR spectra and negative sign of the optical rotation.
Key concepts: Hydrolysate, Absolute configuration, Chemistry, Stereochemistry, Antimicrobial, NMR spectra database, Optical rotation, Hydroxyproline