N-Phenylacetylation and Nonribosomal Peptide Synthetases with Substrate Promiscuity for Biosynthesis of Heptapeptide Variants, JBIR-78 and JBIR-95-Reference-Cited by-同舟云学术

N-Phenylacetylation and Nonribosomal Peptide Synthetases with Substrate Promiscuity for Biosynthesis of Heptapeptide Variants, JBIR-78 and JBIR-95

Published:2017-05-19 Issue:7 Volume:12 Page:1813-1819
ISSN:1554-8929
Container-title:ACS Chemical Biology
language:en
Short-container-title:ACS Chem. Biol.

Author:

Takeda Kunpei¹,Kemmoku Kohei¹,Satoh Yasuharu¹^ORCID,Ogasawara Yasushi¹,Shin-ya Kazuo²,Dairi Tohru¹^ORCID

Affiliation:

1. Graduate School of Engineering, Hokkaido University, N13-W8, Kita-ku, Sapporo, Hokkaido 060-8628, Japan

2. Biomedicinal Information Research Center (BIRC), National Institute of Advanced Industrial Science and Technology (AIST), 2-4-7 Aomi, Koto-ku, Tokyo 135-0064, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Molecular Medicine,General Medicine,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acschembio.7b00314

Reference21 articles.

1. Assembly-Line Enzymology for Polyketide and Nonribosomal Peptide Antibiotics: Logic, Machinery, and Mechanisms

2. New Insights into the Biosynthetic Logic of Ribosomally Synthesized and Post-translationally Modified Peptide Natural Products

3. Ribosome-independent biosynthesis of biologically active peptides: Application of synthetic biology to generate structural diversity

4. A new family of ATP-dependent oligomerization-macrocyclization biocatalysts

5. A stand-alone adenylation domain forms amide bonds in streptothricin biosynthesis

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