Laccase localized in hulle cells and cleistothecial primordia of Aspergillus nidulans

Several species of the genus Aspergillus form sexual spores within minute (approximately 0.2 mm) spherical shells (cleisthothecia) which are woven from specialized hyphae. Aspergillus nidulans cleistothecia are uniquely characterized by their dark red coloration and an envelope of thick-walled globose cells (hulle cells). By use of a new chromogenic substrate, we have shown that the constitutent hyphae of young cleistothecia and the hulle cells which surround the cleistothecia of A. nidulans exhibit a strong phenoloxidase activity which has the substrate specificity of a laccase. This enzyme (laccase II) is distinct from the previously described phenoloxidase (laccase I) that participates in the synthesis of the conidial pigment of A. nidulans: the two enzymes differ electrophoretically, do not cross-react immunologically, appear at different times during colonial development, and are under different genetic control. Examination of seven additional species of Aspergillus showed that the hulle cells of three acleistothecial species were also laccase positive, whereas the pale or unpigmented cleistothecia of four species (which lack hulle cells) were laccase negative. The relevance of these findings to the role of hulle cells in cleistothecial development is discussed. The presence of histologically detectable laccase in cleistothecial primordia provides a valuable tool, previously unavailable, for quantitating the early stages of sexual development in A. nidulans.

[1]  M. Kurtz,et al.  Purification and characterization of the conidial laccase of Aspergillus nidulans , 1982, Journal of bacteriology.

[2]  M. Kurtz,et al.  Dominant spore color mutants of Aspergillus nidulans defective in germination and sexual development , 1981, Journal of bacteriology.

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

[4]  D. Wood,et al.  Production, Purification and Properties of Extracellular Laccase of Agaricus bisporus , 1980 .

[5]  G. Hooper,et al.  Ultrastructure and cytochemical localization of laccase in two strains of Leptosphaerulina briosiana (Pollaci) Graham and Luttrell , 1979, Journal of bacteriology.

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

[7]  B. Bainbridge,et al.  Phenoloxidases of Aspergillus nidulans , 1974 .

[8]  K. Eriksson,et al.  Purification and Properties of Neurospora crassa Laccase , 1974, Journal of bacteriology.

[9]  T. Leonard Phenoloxidase Activity in Mycelia Carrying Modifier Mutations That Affect Sporocarp Development in Schizophyllum commune , 1972, Journal of bacteriology.

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

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

[12]  A. Clutterbuck A mutational analysis of conidial development in Aspergillus nidulans. , 1969, Genetics.

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

[14]  D. Apirion Formal and physiological genetics of ascospore colour in Aspergillus nidulans , 1963 .

[15]  R. Mosbach Purification and some properties of laccase from Polyporus versicolor. , 1963, Biochimica et biophysica acta.

[16]  H. Ljunggren,et al.  Substrate specificity of a purified fungal laccase. , 1961, Biochimica et biophysica acta.

[17]  S. Neelakantan,et al.  Studies in the biochemistry of micro-organisms. 101. The colouring matters of species in the Aspergillus nidulans group. 2. Further observations on the structure of asperthecin. , 1957, The Biochemical journal.

[18]  G. Martin The Genus Aspergillus. , 1946, Science.