» Articles » PMID: 3925881

Biosynthetic Relationship Among Aflatoxins B1, B2, M1, and M2

Overview
Date 1985 Jun 1
PMID 3925881
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

Aflatoxins are a family of toxic, acetate-derived decaketides that arise biosynthetically through polyhydroxyanthraquinone intermediates. Most studies have assumed that aflatoxin B1 is the biosynthetic precursor of the other aflatoxins. We used a strain of Aspergillus flavus which accumulates aflatoxin B2 to investigate the later stages of aflatoxin biosynthesis. This strain produced aflatoxins B2 and M2 but no detectable aflatoxin B1 when grown over 12 days in a low-salt, defined growth medium containing asparagine. Addition of dichlorvos to this growth medium inhibited aflatoxin production with concomitant accumulation of versiconal hemiacetal acetate. When mycelial pellets were grown for 24, 48, and 72 h in growth medium and then transferred to a replacement medium, only aflatoxin B2 and M2 were recovered after 96 h of incubation. Addition of sterigmatocystin to the replacement medium led to the recovery of higher levels of aflatoxins B2 and M2 than were detected in control cultures, as well as to the formation of aflatoxins B1 and M1 and O-methylsterigmatocystin. These results support the hypothesis that aflatoxins B1 and B2 can arise independently via a branched pathway.

Citing Articles

Formation of B- and M-group aflatoxins and precursors by Aspergillus flavus on maize and its implication for food safety.

Schamann A, Schmidt-Heydt M, Geisen R, Kulling S, Soukup S Mycotoxin Res. 2022; 38(2):79-92.

PMID: 35288866 PMC: 9038868. DOI: 10.1007/s12550-022-00452-4.


Electrochemical impedimetric biosensors for food safety.

Chai C, Oh S Food Sci Biotechnol. 2020; 29(7):879-887.

PMID: 32582450 PMC: 7297935. DOI: 10.1007/s10068-020-00776-w.


Synthesis of sterigmatocystin derivatives and their biotransformation to aflatoxins by a blocked mutant of Aspergillus parasiticus.

Gengan R, Chuturgoon A, Mulholland D, Dutton M Mycopathologia. 1999; 144(2):115-22.

PMID: 10481291 DOI: 10.1023/a:1007064304292.


Stereochemistry during aflatoxin biosynthesis: cyclase reaction in the conversion of versiconal to versicolorin B and racemization of versiconal hemiacetal acetate.

Yabe K, Hamasaki T Appl Environ Microbiol. 1993; 59(8):2493-500.

PMID: 8368837 PMC: 182311. DOI: 10.1128/aem.59.8.2493-2500.1993.


Preparation of 4,15-diacetoxyscirpenol from cultures of Fusarium sambucinum NRRL 13495.

Richardson K, Hamilton P Appl Environ Microbiol. 1987; 53(2):460-2.

PMID: 3566274 PMC: 203683. DOI: 10.1128/aem.53.2.460-462.1987.


References
1.
van Walbeek W, Scott P, THATCHER F . Mycotoxins from food-borne fungi. Can J Microbiol. 1968; 14(2):131-7. DOI: 10.1139/m68-022. View

2.
Reddy T, Viswanathan L, Venkitasubramanian T . High aflatoxin production on a chemically defined medium. Appl Microbiol. 1971; 22(3):393-6. PMC: 376320. DOI: 10.1128/am.22.3.393-396.1971. View

3.
Schroeder H, Carlton W . Accumulation of only aflatoxin B 2 by a strain of Aspergillus flavus. Appl Microbiol. 1973; 25(1):146-8. PMC: 380751. DOI: 10.1128/am.25.1.146-148.1973. View

4.
Maggon K, Venkitasubramanian T . Metabolism of aflatoxins B1 and G1 by Aspergillus parasiticus. Experientia. 1973; 29(10):1210-1. DOI: 10.1007/BF01935075. View

5.
Yao R, Hsieh D . Step of dichlorvos inhibition in the pathway of aflatoxin biosynthesis. Appl Microbiol. 1974; 28(1):52-7. PMC: 186587. DOI: 10.1128/am.28.1.52-57.1974. View