Shusuke Sato

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Assistant Professor

Japan

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About

Shusuke Sato is an Assistant Professor at the Institute of Science Tokyo, Japan. His research areas focus on biosynthetic pathways in fungi and bacteria, elucidating mechanisms involved in the biosynthesis of polyketides, glycosylation, and radical S-adenosyl-L-methionine enzymes. Recent articles authored by Professor Sato explore topics such as the identification of biochemical pathways and the reconstitution of biosynthetic pathways, contributing to a deeper understanding of natural product biosynthesis.

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Grant: Close

炭素-炭素結合形成に関わるラジカルS-アデノシル-L-メチオニン酵素の機能解析

Open Date: 2019-04-01

Close Date: 2021-03-01

Articles (9)

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2025

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2025

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2024

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2023

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2022

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2022

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2021

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2020

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2020

Collaborators (4)

Tadashi EGUCHI

Tokyo Institute of Technology

JAPAN

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Yoshimitsu Hamano

University of Fukui

JAPAN

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Atsushi Minami

Hokkaido University

JAPAN

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Fumitaka Kudo

Associate Professor

Tokyo Institute of Technology

JAPAN

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Shusuke Sato

Research Interests

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About

Recent Grants

Articles (9)

Isolation and Identification of Xanthone, Benzofuran, and Spirolactone Derivatives from <i>Dinemasporium parastrigosum</i> KT4144 and Their Plausible Biosynthetic Pathways

Chain-length preference of trans-acting enoylreductases involved in the biosynthesis of fungal polyhydroxy polyketides

Complete In Vitro Reconstitution of the Apramycin Biosynthetic Pathway Demonstrates the Unusual Incorporation of a β-d-Sugar Nucleotide in the Final Glycosylation Step

Biosynthetic Origin of the Octose Core and Its Mechanism of Assembly during Apramycin Biosynthesis

Mechanism of S-Adenosyl-l-methionine C-Methylation by Cobalamin-dependent Radical S-Adenosyl-l-methionine Methylase in 1-Amino-2-methylcyclopropanecarboxylic Acid Biosynthesis

Identification of the Early Steps in Herbicidin Biosynthesis Reveals an Atypical Mechanism of C-Glycosylation

Biochemical and Mutational Analysis of Radical S-Adenosyl-L-Methionine Adenosylhopane Synthase HpnH from Zymomonas mobilis Reveals that the Conserved Residue Cysteine-106 Reduces a Radical Intermediate and Determines the Stereochemistry

<i>C</i>-Methylation of <i>S</i>-adenosyl-L-Methionine Occurs Prior to Cyclopropanation in the Biosynthesis of 1-Amino-2-Methylcyclopropanecarboxylic Acid (Norcoronamic Acid) in a Bacterium

Characterization of Radical SAM Adenosylhopane Synthase, HpnH, which Catalyzes the 5′‐Deoxyadenosyl Radical Addition to Diploptene in the Biosynthesis of C35 Bacteriohopanepolyols

Collaborators (4)

Tadashi EGUCHI

Yoshimitsu Hamano

Atsushi Minami

Fumitaka Kudo

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