Morita Maho

J-GLOBAL         Last updated: Nov 5, 2019 at 20:16
 
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Morita Maho

Published Papers

 
Paola Estrada, Maho Morita, Yue Hao, Eric W. Schmidt, Satish K. Nair
Journal of the American Chemical Society   140 8124-8127   Jul 2018
© Copyright 2018 American Chemical Society. Mutation at a single amino acid alters the isoprene donor specificity of prenyltransferases involved in the modification of ribosomally synthesized and post-translationally modified peptides (RiPPs). Th...
Maho Morita, Yue Hao, Jouni K. Jokela, Debosmita Sardar, Zhenjian Lin, Kaarina Sivonen, Satish K. Nair, Eric W. Schmidt
Journal of the American Chemical Society   140 6044-6048   May 2018
© 2018 American Chemical Society. Prenylation is a widespread modification that improves the biological activities of secondary metabolites. This reaction also represents a key modification step in biosyntheses of cyanobactins, a family of ribosom...
Maho Morita, Eric W. Schmidt
Natural Product Reports   35 357-378   Apr 2018
© 2018 The Royal Society of Chemistry. Covering: up to 2018 Symbiotic microbes interact with animals, often by producing natural products (specialized metabolites; secondary metabolites) that exert a biological role. A major goal is to determine w...
Sato E, Morita M, Ogawa H, Iwatsuki M, Hokari R, Ishiyama A, Ōmura S, Iwasaki A, Suenaga K
Bioorganic & medicinal chemistry letters   28(3) 298-301   Feb 2018   [Refereed]
Cui J, Morita M, Ohno O, Kimura T, Teruya T, Watanabe T, Suenaga K, Shibasaki M
Chemistry (Weinheim an der Bergstrasse, Germany)   23(35) 8500-8509   Jun 2017   [Refereed]
Debosmita Sardar, Yue Hao, Zhenjian Lin, Maho Morita, Satish K. Nair, Eric W. Schmidt
Journal of the American Chemical Society   139 2884-2887   Mar 2017
© 2017 American Chemical Society. Recent innovations in peptide natural product biosynthesis reveal a surprising wealth of previously uncharacterized biochemical reactions that have potential applications in synthetic biology. Among these, the cya...
Yue Hao, Elizabeth Pierce, Daniel Roe, Maho Morita, John A. McIntosh, Vinayak Agarwal, Thomas E. Cheatham, Eric W. Schmidt, Satish K. Nair
Proceedings of the National Academy of Sciences of the United States of America   113 14037-14042   Dec 2016
The cyanobactin prenyltransferases catalyze a series of known or unprecedented reactions on millions of different substrates, with no easily observable recognition motif and exquisite regioselectivity. Here we define the basis of broad substrate t...
海洋天然物ビセリングビアサイド類の作用機序研究–カルシウムポンプを標的とするシアノバクテリア由来のマクロリド
Maho Morita, Haruo Ogawa, Kiyotake Suenaga, Chikashi Toyoshima
Chemistry and biology   54 710-712   2016   [Refereed]
Iwasaki A, Ohno O, Katsuyama S, Morita M, Sasazawa Y, Dan S, Simizu S, Yamori T, Suenaga K
Bioorganic & medicinal chemistry letters   25(22) 5295-5298   Nov 2015   [Refereed]
Morita M, Ogawa H, Ohno O, Yamori T, Suenaga K, Toyoshima C
FEBS letters   589(13) 1406-1411   Jun 2015   [Refereed]
Biselyngbyolide B, a novel ER stress-inducer isolated from the marine cyanobacterium Lyngbya sp.
Ohno, O.; Watanabe, A.; Morita, M.; Suenaga, K.
Chemistry letters   43 287-289   2014   [Refereed]
Ohno O, Morita M, Kitamura K, Teruya T, Yoneda K, Kita M, Kigoshi H, Suenaga K
Bioorganic & medicinal chemistry letters   23(5) 1467-1471   Mar 2013   [Refereed]
A novel allelopathic active substance, 13-epi-orthosiphol N, in Orthosiphon stamineus
Kato-Noguchi, H.; Hamada, N.; Morita, M.; Suenaga, K.
Journal of plant physiology   170 1-5   2013   [Refereed]
Organ-specific-active allelopathic substance in red pine needles
Kato-Noguchi H. Fushimi Y. Kimura, F. Morita M. Suenaga K.
Plant growth regulation   68 171-175   Nov 2012   [Refereed]
Kita M, Yoneda K, Hirayama Y, Yamagishi K, Saito Y, Sugiyama Y, Miwa Y, Ohno O, Morita M, Suenaga K, Kigoshi H
ChemBioChem   13 1754-1758   Aug 2012   [Refereed]
Isolation and structures of biselyngbyasides B, C, and D from the marine cyanobacterium Lyngbya sp., and the biological activities of biselyngbyasides.
Morita M. Ohno O. Teruya T. Yamori T. Inuzuka T. Suenaga K.
Tetrahedron   68 5984-5990   May 2012   [Refereed]
Biselyngbyolide A, a novel cytotoxic macrolide from the marine cyanobacterium Lyngbya sp.
Morita M. Ohno O. Suenaga K.
Chemistry letters   35 357-358   Feb 2012   [Refereed]