Avermectin B2 O-methyltransferase activity in "Streptomyces avermitilis" mutants that produce increased amounts of the avermectins

The level of activity of avermectin B O-methyltransferase, the enzyme which catalyzes the conversion of avermectin B components to avermectin A components, was analyzed in a series of "Streptomyces avermitilis" mutants selected for increased production of the avermectins. In all of the mutants, increased avermectin production was accompanied by increased avermectin B O-methyltransferase activity. Both the average specific activity and the maximum observed specific activity of avermectin B O-methyltransferase increased in direct proportion to avermectin production. The level of avermectin B O-methyltransferase alone did not determine the extent of conversion of avermectin B components to avermectin A components, since a constant ratio of B components to A components was maintained throughout the fermentation even though avermectin B O-methyltransferase specific activity varied three- to fivefold. These results indicate that avermectin B O-methyltransferase is not rate limiting. The correlation between avermectin B O-methyltransferase specific activity and avermectin production is compatible with the hypothesis that genes coding for successive steps in the same secondary metabolite biosynthetic pathway are coordinately regulated.

[1]  O. Hensens,et al.  Demethylavermectins. Biosynthesis, isolation and characterization. , 1985, The Journal of antibiotics.

[2]  D. Hopwood,et al.  Molecular cloning of the whole biosynthetic pathway of a Streptomyces antibiotic and its expression in a heterologous host , 1984, Nature.

[3]  R. H. Baltz,et al.  S-Adenosyl-L-methionine: macrocin O-methyltransferase activities in a series of Streptomyces fradiae mutants that produce different levels of the macrolide antibiotic tylosin , 1982, Antimicrobial Agents and Chemotherapy.

[4]  R. H. Baltz,et al.  Properties of S-adenosyl-L-methionine:macrocin O-methyltransferase in extracts of Streptomyces fradiae strains which produce normal or elevated levels of tylosin and in mutants blocked in specific O-methylations , 1981, Antimicrobial Agents and Chemotherapy.

[5]  J. Springer,et al.  The absolute stereochemistry and conformation of avermectin B2a aglycone and avermectin B1a , 1981 .

[6]  A. W. Douglas,et al.  AVERMECTINS. STRUCTURE DETERMINATION , 1981 .

[7]  K. Wilson,et al.  Avermectins, New Family of Potent Anthelmintic Agents: Isolation and Chromatographic Properties , 1979, Antimicrobial Agents and Chemotherapy.

[8]  S. Ōmura,et al.  Avermectins, New Family of Potent Anthelmintic Agents: Producing Organism and Fermentation , 1979, Antimicrobial Agents and Chemotherapy.

[9]  J. Corcoran S-adenosylmethionine:erythromycin C O-methyltransferase. , 1975, Methods in enzymology.

[10]  S. Zamenhof [103] Preparation and assay of deoxyribonucleic acid from animal tissue , 1957 .