Literature DB >> 16349759

Microbial conversion of acetanilide to 2'-hydroxyacetanilide and 4'-hydroxyacetanilide.

R J Theriault1, T H Longfield.   

Abstract

Approximately 700 cultures of various types were examined for their ability to hydroxylate acetanilide. The major product formed by unidentified Streptomyces species RJTS-539 was identified as 4'-hydroxyacetanilide (N-acetyl-p-aminophenol). This culture gave a peak yield of 405 mg per liter from 1,000 mg of acetanilide per liter. Considerably lower yields of 4'-hydroxyacetanilide were isolated from S. cinnamoneus NRRLB-1285. The major conversion product of acetanilide formed by Amanita muscaria F-6 was identified as 2'-hydroxyacetanilide, with a peak yield of 433 mg per liter from 1,000 mg per liter of substrate. A small amount of 4'-hydroxyacetanilide was also formed. Six other Streptomyces cultures formed small amounts of one or two products identical or similar to 2'-hydroxyacetanilide or 4'-hydroxyacetanilide as determined by thin-layer chromatography and ultraviolet spectra.

Entities:  

Year:  1967        PMID: 16349759      PMCID: PMC547222          DOI: 10.1128/am.15.6.1431-1436.1967

Source DB:  PubMed          Journal:  Appl Microbiol        ISSN: 0003-6919


  1 in total

1.  Ascorbic acid in aromatic hydroxylation. II. Products formed by reaction of substrates with ascorbic acid, ferrous ion, and oxygen.

Authors:  B B BRODIE; J AXELROD; P A SHORE; S UDENFRIEND
Journal:  J Biol Chem       Date:  1954-06       Impact factor: 5.157

  1 in total
  1 in total

1.  Biotransformation of nitro aromatic amines in artificial alkaline habitat by pseudomonas DL17.

Authors:  Vasudeo Sarwade; Sharad Funde
Journal:  Environ Anal Health Toxicol       Date:  2022-02-03
  1 in total

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