Characterizing <scp>Post‐PKS</scp> Modifications of <scp>16‐Demethyl</scp> ‐rifamycin Revealed Two Dehydrogenases Diverting the Aromatization Mode of Naphthalenic Ring in Ansamycin Biosynthesis-Reference-Cited by-同舟云学术

Characterizing Post‐PKS Modifications of 16‐Demethyl ‐rifamycin Revealed Two Dehydrogenases Diverting the Aromatization Mode of Naphthalenic Ring in Ansamycin Biosynthesis

Published:2022-04-22 Issue:13 Volume:40 Page:1553-1558
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Han Ting‐Yan¹,Zhang Kai¹,Tang Gong‐Li¹²,Zhou Qiang¹

Affiliation:

1. State Key Laboratory of Bio‐organic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences 345 Lingling Road Shanghai 200032 China

2. School of Chemistry and Materials Science, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences 1 Sublane Xiangshan Hangzhou Zhejiang 310024 China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.202200098

Reference21 articles.

1. Biosynthesis of 3,5-AHBA-derived natural products

2. From Ergot to Ansamycins45 Years in Biosynthesis

3. Rifamycins – Obstacles and opportunities

4. Identification of tailoring genes involved in the modification of the polyketide backbone of rifamycin B by Amycolatopsis mediterranei S699

5. Direct evidence that the rifamycin polyketide synthase assembles polyketide chains processively

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