Comparison of the omtA genes encoding O-methyltransferases involved in aflatoxin biosynthesis from Aspergillus

J Yu1, P K Chang, G A Payne

  • 1USDA/ARS, Southern Regional Research Center, New Orleans, LA 70179, USA.

Gene
|September 22, 1995
PubMed

Insights

O-methyltransferase (OMT) is crucial for aflatoxin production in Aspergillus fungi. This study sequenced the omtA gene in Aspergillus parasiticus and Aspergillus flavus, finding high sequence identity and conserved intron structures.

Area of Science:

  • Mycology
  • Molecular Biology
  • Biochemistry

Background:

  • Aflatoxins (AF) are toxic secondary metabolites produced by Aspergillus fungi.
  • O-methyltransferase (OMT) is a key enzyme in the AF biosynthesis pathway.
  • Understanding the omtA gene is vital for controlling AF contamination.

Purpose of the Study:

  • To sequence and analyze the omtA gene in Aspergillus parasiticus (Ap) and Aspergillus flavus (Af).
  • To compare the genomic and cDNA sequences of the omtA gene between these two fungal species.
  • To identify conserved regions and structural features of the omtA gene.

Main Methods:

  • Genomic DNA cloning and sequencing of the omtA gene from Ap strain SRRC 143 and Af strain CRA01-2B.
  • Comparison of genomic DNA sequences with cDNA sequences.
  • Sequence alignment and identity analysis.

Main Results:

  • The omtA gene was successfully sequenced in both Ap and Af.
  • Four introns, 52-60 bp in length, were identified in the omtA gene of both species.
  • The S-adenosylmethionine-binding motif was located between the third and fourth introns.
  • The coding sequences of omtA from Ap and Af showed over 97% identity.

Conclusions:

  • The omtA gene structure, including intron number and location, is conserved between Aspergillus parasiticus and Aspergillus flavus.
  • High sequence identity in the coding region suggests functional conservation of OMT in aflatoxin biosynthesis.
  • These findings provide a basis for further research into OMT function and AF control strategies.