Literature DB >> 20062868

Engineered transaminopeptidase, aminolysin-S for catalysis of peptide bond formation to give linear and cyclic dipeptides by one-pot reaction.

Hirokazu Usuki1, Yoshiko Uesugi, Jiro Arima, Yukihiro Yamamoto, Masaki Iwabuchi, Tadashi Hatanaka.   

Abstract

Aminopeptidase from Streptomyces thermocyaneoviolaceus NBRC14271 was engineered into transaminopeptidase and used to catalyze an aminolysis reaction to give linear and cyclic dipeptides from cost-effective substrates such as the ester derivatives of amino acids.

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Year:  2009        PMID: 20062868     DOI: 10.1039/b914320c

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  Prolyl aminopeptidase from Streptomyces thermoluteus subsp. fuscus strain NBRC14270 and synthesis of proline-containing peptides by its S144C variant.

Authors:  Yukihiro Yamamoto; Hirokazu Usuki; Masaki Iwabuchi; Tadashi Hatanaka
Journal:  Appl Environ Microbiol       Date:  2010-07-30       Impact factor: 4.792

2.  One-pot synthesis of diverse DL-configuration dipeptides by a Streptomyces D-stereospecific amidohydrolase.

Authors:  Jiro Arima; Hirokazu Usuki; Tadashi Hatanaka; Nobuhiro Mori
Journal:  Appl Environ Microbiol       Date:  2011-09-23       Impact factor: 4.792

3.  The aminolysis reaction of streptomyces S9 aminopeptidase promotes the synthesis of diverse prolyl dipeptides.

Authors:  Jiro Arima; Masazumi Morimoto; Hirokazu Usuki; Nobuhiro Mori; Tadashi Hatanaka
Journal:  Appl Environ Microbiol       Date:  2010-04-23       Impact factor: 4.792

  3 in total

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