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s - Mycological Society of America

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were transferred to minimal plates from two radii.<br />

From the remaining six radii three mycelial blocks<br />

from the outer, middle and central portions <strong>of</strong> the<br />

colony were .transferred to minimal media and minimal<br />

media supplemented with one <strong>of</strong> the parental require-<br />

ments. Results indicate that heterokaryotic regions<br />

do not extend beyond the central portion <strong>of</strong> the colony<br />

In sane cases both auxotrophic canponents were uni-<br />

formly distributed in the outer region <strong>of</strong> the colony.<br />

In other heterokaryons only one parenk was found at<br />

the periphery <strong>of</strong> the colony. 'Ihis study suggests that<br />

the auxotrophic portion <strong>of</strong> the colony is nutritionally<br />

supplemented by a smaller prototrophic region at the<br />

center <strong>of</strong> the colony.<br />

T.E. CHASE. J. TAYLOR. F.W. COBB. JR.. P.T. SPIETH,<br />

and W.J. OTROSINA. University <strong>of</strong> California.<br />

Berkeley 94720 and USDA-Forest Service Pacific<br />

Southwest Forest and Range Experiment Station.<br />

Berkeley. CA 94701.<br />

Mitochondria1 DNA differences among biological<br />

species <strong>of</strong> Heterobasidion annosum.<br />

H. annosum, a basidiomycete root- and butt-rot<br />

fungus <strong>of</strong> conifers. contains several biological<br />

species (intersterility groups). Previous mating<br />

tests and isozyme studies (which assess primarily<br />

nuclear encoded genes) indicate that the S and P<br />

groups in the western United States have undergone<br />

a high degree <strong>of</strong> genetic divergence and that there<br />

is no gene flow between them. In order to assess<br />

the cytoplasmic genome, we analyzed mitochondria1<br />

DNA restriction fragment length polymorphisms<br />

(mtDNA RFLPs) with a rapid screening method<br />

employing the Hae 111 restriction endonuclease.<br />

RFLP patterns for S group strains from North<br />

<strong>America</strong> were clearly different from P group strains<br />

from North <strong>America</strong>. In addition. differences in<br />

Rm9 patterns exist between European and North<br />

<strong>America</strong>n S group strains. These results are<br />

consistent with our earlier studies based on<br />

nuclear genes. both <strong>of</strong> which demonstrated that the<br />

biological species <strong>of</strong> K. annosum represent well<br />

separated gene pools.<br />

T.E. CHASE and R.C. ULLRICH. Plant Pathology<br />

Dept.. University <strong>of</strong> California, Berkeley 94720<br />

and Botany Dept.. University <strong>of</strong> Vermont.<br />

Burlington 05405.<br />

"Illegitimate" mating in Heterobasidion annosum.<br />

In previous studies we showed that intersterility<br />

in H. annosum is regulated by five genes.<br />

designated Vl+/Vl-. V2+/V2-. V3+/V3-. S+/e,<br />

P+/k.<br />

Any two homokaryotic strains are<br />

interfertile (able to form dikaryons) if they are<br />

homoallelic for + alleles at one or more <strong>of</strong> these<br />

loci and also carry compatible mating-type<br />

alleles. Cases in which intersterile pairings<br />

give rise to putative dikaryons are reported<br />

here. Such "illegitimate" mating occurs<br />

inconsistently, but is more frequent when<br />

pairings are incubated for a prolonged (30 day)<br />

period rather than the normal 10 day period prior<br />

to the routine subculturing step which is part <strong>of</strong><br />

the mating protocol. Analysis <strong>of</strong> progeny derived<br />

from an illegitimate mating suggest a genetic<br />

model in which parasexuality may play a role in<br />

generating nuclei containing recombinant<br />

genotypes which are interfertile and compatible<br />

with one <strong>of</strong> the progenitor nuclei. Illegitimate<br />

mating thus represents a special case <strong>of</strong><br />

intersterile and interfertile mating behavior.<br />

because the dikaryons resulting from such events<br />

contain two genomes with + alleles in common at<br />

at least one <strong>of</strong> the five loci. Ability to engage<br />

in illegitimate mating is a strain-specific<br />

characteristic but does not appear to be<br />

inherited as a simple Mendelian trait.<br />

A. W. CHEN. Russell Res. Ctr. PPRU. P.O. Box 5677.<br />

Athens, CA 30613. Transition to reproduction in<br />

Fanodema Jucidum and other basidiomycetes.<br />

Six stages (grovth in vegetative medium, grovth in<br />

fruiting medium, transition to basidiocarp primor-<br />

dium formation, stipe formation, growth <strong>of</strong> pileus,<br />

and tube & spore formation) are identified in G.<br />

lucidum during transition to sexual reproduction.<br />

Cultures continue to grow vegetatively, or only<br />

abortive fruiting bodies (vithout tube & spore for-<br />

mation) will be obtained if proper cultural parame-<br />

ters are not maintained. These parameters include<br />

medium components (carbon source, C/N ratio, thia-<br />

mine, pH and texture), and abiotic factors for<br />

incubation (temperature, light/darkness. COJventi-<br />

lation, and moisture). Methodology on fruiting in-<br />

duction in s. lucidum is reviewed. Usually shifting<br />

from groving inoculum or spawn in vegetative medium<br />

to fruiting medium containing more complex carbohy-<br />

drates is involved. Of critical importance are: 1)<br />

transition to basidiocarp-primordium formation, and<br />

2) transition to tube h spore formation. Damaging or<br />

killing cells in fruiting cultures can induce pri-<br />

mordia or tube & spore formation. When vorking vith<br />

un-defined and heterogenous fruiting media, such as<br />

vood or sawdust, and bran or corn meal, or using<br />

induction techniques vith no specific effects, the<br />

results are not always consistent. The underlined<br />

processes during transition to basidiocarp formation<br />

(storage and utilization <strong>of</strong> energy sources, change<br />

<strong>of</strong> mycelial growth pattern, light induction, lipid<br />

synthesis, enzyme activities and ultra-structural<br />

studies on tube and spore formation) are selectively<br />

reviewed including other basidiomycetes.<br />

CHD-CHOU, 2. -Q. AN, J. 1. HENDRIX, Q.<br />

ZKAI, and H. R. BIEGEL. Department <strong>of</strong> Plant<br />

Pathology, University <strong>of</strong> Kentucky, Lexington<br />

40546.<br />

Effect <strong>of</strong> the Acremonium endophyte on<br />

endogonaceous mycorrhizal fungi reproducing<br />

on tall fescue.<br />

Soil samples taken from field plots planted<br />

to tall fescue (cv. Ky 31) with low or high<br />

levels <strong>of</strong> the hcremonium coenowhialum<br />

endophyte were assayed for endogonaceous<br />

propagules by an MPN bioassay procedure.<br />

Soil from low-endophyte plots contained more<br />

propagules and species than soil front high-<br />

endophyte plots. Pure cultures <strong>of</strong> one<br />

isolate <strong>of</strong> Glomus mosseae and two isolates

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