Literature DB >> 8476299

Secondary metabolites resulting from degradation of PR toxin by Penicillium roqueforti.

S C Chang1, K L Lu, S F Yeh.   

Abstract

PR toxin is a secondary metabolite of the fungus Penicillium roqueforti. It is lethal to rats, mice, and cats. Usually, the amount of PR toxin in the culture medium decreases from its maximum on day 15 to zero within 3 to 4 days. We found that two were secondary metabolites produced in the culture medium of this fungus while the production of PR toxin was decreasing. We isolated and purified the two compounds in pure and colorless crystalline form. On the basis of elemental analysis and mass, 1H and 13C nuclear magnetic resonance, infrared, and UV spectroscopies, the two compounds were identified as PR-imine (C17H21O5N) and PR-amide (C17H21O6N). The structures of both compounds and of PR toxin (C17H20O6) were closely related, and the peak production of PR toxin appeared earlier than those of PR-imine and PR-amide. Moreover, PR toxin was transformed to PR-imine when PR toxin was incubated with the culture medium on a given culture day. Thus, we propose that PR toxin is degraded into PR-imine and PR-amide in the culture medium of P. roqueforti.

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Year:  1993        PMID: 8476299      PMCID: PMC202226          DOI: 10.1128/aem.59.4.981-986.1993

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  14 in total

1.  Genetic effects of PR toxin in eukaryotic microorganisms.

Authors:  R Wei; T Ong; W Whong; D Frezza; G Bronzetti; E Zeiger
Journal:  Environ Mutagen       Date:  1979

2.  Mechanism of the inhibition of transcription by PR toxin, a mycotoxin from Penicillium roqueforti.

Authors:  Y Moulé; M Jemmali; N Rousseau
Journal:  Chem Biol Interact       Date:  1976-08       Impact factor: 5.192

3.  Production of Eremofortins A, B, and C Relative to Formation of PR Toxin by Penicillium roqueforti.

Authors:  S Moreau; A Lablache-Combier; J Biguet
Journal:  Appl Environ Microbiol       Date:  1980-04       Impact factor: 4.792

4.  In vitro metabolism of penicillium roqueforti toxin (PRT) and a structurally related compound, eremofortin A, by rat liver.

Authors:  M Cacan; S Moreau; R Tailliez
Journal:  Toxicology       Date:  1977-10       Impact factor: 4.221

5.  Eremofortin C.A new metabolite obtained from penicillium roqueforti cultures and from biotransformation of PR toxin.

Authors:  S Moreau; M Cacan
Journal:  J Org Chem       Date:  1977-07-22       Impact factor: 4.354

6.  Biochemical effects of PR toxin on rat liver mitochondrial respiration and oxidative phosphorylation.

Authors:  Y H Wei; W H Ding; R D Wei
Journal:  Arch Biochem Biophys       Date:  1984-05-01       Impact factor: 4.013

7.  Inhibition of protein synthesis by PR toxin, a mycotoxin from Penicillium roqueforti.

Authors:  Y Moulé; M Jammali; N Darracq
Journal:  FEBS Lett       Date:  1978-04-15       Impact factor: 4.124

8.  Resolution of Penicillium roqueforti toxin and eremofortins A, B, and C by high-performance liquid chromatography.

Authors:  S Moreau; A Masset; J Biguet
Journal:  Appl Environ Microbiol       Date:  1979-06       Impact factor: 4.792

9.  Isolation and partial characterization of a mycotoxin from Penicillium roqueforti.

Authors:  R D Wei; P E Still; E B Smalley; H K Schnoes; F M Strong
Journal:  Appl Microbiol       Date:  1973-01

10.  Acute toxicity of PR toxin, a mycotoxin from Penicillium roqueforti.

Authors:  F C Chen; C F Chen; R D Wei
Journal:  Toxicon       Date:  1982       Impact factor: 3.033

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  2 in total

1.  Isolation, purification, and characterization of the PR oxidase from penicillium roqueforti

Authors: 
Journal:  Appl Environ Microbiol       Date:  1998-12       Impact factor: 4.792

Review 2.  Germacrene A-A Central Intermediate in Sesquiterpene Biosynthesis.

Authors:  Houchao Xu; Jeroen S Dickschat
Journal:  Chemistry       Date:  2020-09-30       Impact factor: 5.236

  2 in total

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