Department of Chemical and Biological Sciences, Oregon Graduate Center, Beaverton, Oregon 97006-1999.
Appl Environ Microbiol. 1987 Jul;53(7):1464-9. doi: 10.1128/aem.53.7.1464-1469.1987.
Prototrophic strains recovered from crosses between auxotrophic strains of the lignin-degrading basidiomycete Phanerochaete chrysosporium were induced to fruit. The progeny of most of these self-crosses were prototrophic, indicating that the nuclei of the original prototroph were wild-type recombinants rather than complementary heterokaryons and that the binucleate basidiospores of this organism are homokaryotic. Various wild-type strains were shown to have multinucleate cells lacking clamp connections and to possess a variable number of sterigmata per basidium. Colonies arising from single conidia of various wild-type strains were all capable of producing fruit bodies and basidiospores. In addition, single basidiospores from three wild-type strains all produced fruit bodies and basidiospores. Nonfruiting as well as fruiting isolates were obtained from single basidiospores of five other wild-type strains. Basidiospores from these fruiting isolates always yielded colonies that fruited, again indicating that the spores are homokaryotic. Nonfruiting isolates from the same strain did not produce basidiospores when allowed to form a heterokaryon, implying that these isolates do not represent mating types. All this evidence indicates that P. chrysosporium has a primary homothallic mating system. In addition to fruiting and nonfruiting phenotypes, basidiospores from strain OGC101, a derivative of ME-446, gave rise to colonies which did not grow on cellulose (Cel). The fruiting, nonfruiting, and Cel phenotypes differed from each other and from the parental wild-type strain in a variety of characteristics, including growth, conidiation, and evolution of CO(2) from C-side chain-labeled lignin, indicating that strain OCG101 is a heterokaryon.
从木质素降解担子菌糙皮侧耳(Phanerochaete chrysosporium)营养缺陷型菌株杂交中恢复的原养型菌株被诱导结实。这些自交的大多数后代都是原养型的,这表明原始原养型的核是野生型重组体,而不是互补异核体,并且该生物体的双核担子孢子是同核的。各种野生型菌株显示出多核细胞缺乏扣状连接,并具有每个担子每一个不定数目的小梗。来自各种野生型菌株的单个分生孢子产生的菌落都能够产生子实体和担子孢子。此外,来自三个野生型菌株的单个担子孢子都产生了子实体和担子孢子。从五个其他野生型菌株的单个担子孢子中获得了非结实和结实的分离株。从这些结实的分离株中获得的担子孢子总是产生结实的菌落,这再次表明孢子是同核的。从同一菌株中获得的非结实分离株在形成异核体时不产生担子孢子,这意味着这些分离株不代表交配型。所有这些证据表明糙皮侧耳具有主要的同宗配合交配系统。除了结实和非结实表型外,来自 ME-446 衍生物菌株 OGC101 的担子孢子产生的菌落不能在纤维素(Cel)上生长。结实、非结实和 Cel 表型彼此不同,并且与亲本野生型菌株在各种特征上不同,包括生长、分生孢子形成和 C-侧链标记木质素的 CO(2)的进化,表明菌株 OCG101 是一个异核体。