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Bestatin Analogue fromStreptomyces neyagawaensisSL-387

Authors :
Hyo Kon Chun
Yung Hee Kho
Myung Chul Chung
Choong Hwan Lee
Ho Jae Lee
Su-Il Kim
Source :
Bioscience, Biotechnology, and Biochemistry. 60:898-900
Publication Year :
1996
Publisher :
Informa UK Limited, 1996.

Abstract

A bestatin analogue, (2S,3R)-3-amino-2-hydroxy-4-phenylbutanoyl-L-valine (AHPA-Val), from the culture filtrate of Streptomyces neyagawaensis SL-387 was obtained in a chemically defined medium containing DL-3-amino-3-phenylpropionic acid. AHPA-Val was 6 times (IC50 = 1.2 micrograms/ml) as strong as bestatin (IC50 = 7.0 micrograms/ml) against porcine kidney microsomal aminopeptidase N, and 4 times (5.6 micrograms/ml) as strong as bestatin (IC50 = 20.7 micrograms/ml) against aminopeptidase N of human metastatic fibrosarcoma HT1080. To the best of our knowledge, this is the first report on the microbial production of AHPA-Val.

Details

ISSN :
13476947 and 09168451
Volume :
60
Database :
OpenAIRE
Journal :
Bioscience, Biotechnology, and Biochemistry
Accession number :
edsair.doi.dedup.....b4e229ad2c4cc6c7245cc99f161f44d9
Full Text :
https://doi.org/10.1271/bbb.60.898