Dominant spore color mutants of Aspergillus nidulans defective in germination and sexual development

The ascomycete Aspergillus nidulans produces green conidia (asexual spores). Recessive mutants which produce yellow conidia have been previously isolated from haploid strains and have been shown to be deficient in laccase (diphenol oxidase), an enzyme that requires copper for activity. Using a diploid parent strain, we isolated dominant yellow conidial mutants which, in the haploid state, produced even less laccase activity than a recessive mutant. Three isolates of such mutants behaved similarly and define a single complementation group (yB) on chromosome VIII distinct from the yA locus on chromosome I defined by recessive mutants. Unlike yA mutants, whose only discernable phenotype is their conidial color, yB mutants are pleiotropic: conidial germination was delayed relative to the wild type, and sexual development was blocked at an early stage. The three phenotypes of yB mutants were expressed on yeast extract-glucose medium containing 1.6 microM of added copper. When copper was added to above 5 microM, all three phenotypes were remediated, and near wild-type levels of laccase were produced. We conclude that yB mutants have a reduced availability of copper. The dominance of yB mutants could result, for example, from an alteration in transport or storage of copper. Using an immunological assay, we detected no laccase antigenic cross-reacting material in yB mutants grown on medium of low copper content. We conclude that either the synthesis or the stability of laccase is copper dependent.

[1]  N. Horowitz,et al.  Cellular and extracellular siderophores of Aspergillus nidulans and Penicillium chrysogenum , 1981, Molecular and cellular biology.

[2]  W. Timberlake,et al.  Developmental regulation of laccase levels in Aspergillus nidulans , 1980, Journal of bacteriology.

[3]  K. Lerch Copper metallothionein, a copper-binding protein from Neurospora crassa , 1980, Nature.

[4]  Hurn Ba,et al.  Production of reagent antibodies. , 1980 .

[5]  B. Hurn,et al.  Production of reagent antibodies. , 1980, Methods in enzymology.

[6]  J. Oudin Immunochemical analysis by antigen-antibody precipitation in gels. , 1980, Methods in Enzymology.

[7]  R. Cousins Synthesis and degradation of liver metallothionein. , 1979, Experientia. Supplementum.

[8]  N. Horowitz,et al.  Isolation and identification of the conidial germination factor of Neurospora crassa , 1976, Journal of bacteriology.

[9]  C. Roberts,et al.  Analysis of acetate non-utilizing (acu) mutants in Aspergillus nidulans. , 1976, Journal of general microbiology.

[10]  A. Clutterbuck Gene symbols in Aspergillus nidulans. , 1973, Genetical research.

[11]  T. Leonard,et al.  Study of Phenoloxidase Activity During the Reproductive Cycle in Schizophyllum commune , 1973, Journal of bacteriology.

[12]  A. Clutterbuck,et al.  Absence of laccase from yellow-spored mutants of Aspergillus nidulans. , 1972, Journal of general microbiology.

[13]  T. Leonard Phenoloxidase Activity and Fruiting Body Formation in Schizophyllum commune , 1971, Journal of bacteriology.

[14]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[15]  K. Esser,et al.  The phenoloxidases of the ascomycete Podospora anserina. Communication 4. Genetic regulation of the formation of laccase. , 1970, Genetics.

[16]  K. Esser Phenol oxidases and morphogenesis in Podospora anserina. , 1968, Genetics.

[17]  G. Dorn A revised map of the eight linkage groups of Aspergillus nidulans. , 1967, Genetics.

[18]  D. Cove The induction and repression of nitrate reductase in the fungus Aspergillus nidulans. , 1966, Biochimica et biophysica acta.

[19]  K. D. Macdonald,et al.  The genetics of Aspergillus nidulans. , 1953, Advances in genetics.

[20]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.