Literature DB >> 26689788

A nitrous acid biosynthetic pathway for diazo group formation in bacteria.

Yoshinori Sugai1, Yohei Katsuyama1, Yasuo Ohnishi1.   

Abstract

Although some diazo compounds have bioactivities of medicinal interest, little is known about diazo group formation in nature. Here we describe an unprecedented nitrous acid biosynthetic pathway responsible for the formation of a diazo group in the biosynthesis of the ortho-diazoquinone secondary metabolite cremeomycin in Streptomyces cremeus. This finding provides important insights into the biosynthetic pathways not only for diazo compounds but also for other naturally occurring compounds containing nitrogen-nitrogen bonds.

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Year:  2015        PMID: 26689788     DOI: 10.1038/nchembio.1991

Source DB:  PubMed          Journal:  Nat Chem Biol        ISSN: 1552-4450            Impact factor:   15.040


  26 in total

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  24 in total

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3.  Recycling of Overactivated Acyls by a Type II Thioesterase during Calcimycin Biosynthesis in Streptomyces chartreusis NRRL 3882.

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Review 4.  Heteroatom-Heteroatom Bond Formation in Natural Product Biosynthesis.

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Review 5.  Diazo Compounds: Versatile Tools for Chemical Biology.

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6.  A heme-dependent enzyme forms the nitrogen-nitrogen bond in piperazate.

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7.  Identifying the Biosynthetic Gene Cluster for Triacsins with an N-Hydroxytriazene Moiety.

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8.  The l-Alanosine Gene Cluster Encodes a Pathway for Diazeniumdiolate Biosynthesis.

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9.  A Mutasynthetic Library of Platensimycin and Platencin Analogues.

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10.  PcxL and HpxL are flavin-dependent, oxime-forming N-oxidases in phosphonocystoximic acid biosynthesis in Streptomyces.

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