s - Mycological Society of America
s - Mycological Society of America
s - Mycological Society of America
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E.A. MOMOL. J.W. KIMBROUGH, and H.C. KISTLER.<br />
Department <strong>of</strong> Plant Pathology. Universtty <strong>of</strong> Florida,<br />
Gainesville, FL 3261 1.<br />
Electrophoretic karyotypes are dissimilar for two strains <strong>of</strong><br />
Fusarium owsDorum that differ in host range.<br />
Protoplasts were obtained from strains <strong>of</strong> two formae<br />
speciales <strong>of</strong> the wilt pathogen Fusarium owsporum. To<br />
determine if genetic recombination could occur, protoplasts<br />
<strong>of</strong> strain ATCC 9990 E. owsporum 1. sp. conalutinans (a<br />
cabbage pathogen), and <strong>of</strong> strain ATCC 16601 E. owsporum<br />
f. sp. raphani (a radish pathogen) were fused in the presence<br />
<strong>of</strong> PEG. Chromosomes <strong>of</strong> fusants and parental strains were<br />
separated using contour clamped homogenous electrical field<br />
(CHEF) gel electrophoresis. . Karyotypes differed greatly<br />
between strains and minimum number <strong>of</strong> 11 and 8<br />
chromosomal bands were detected for ATCC 16601 and<br />
ATCC 9990 respectively. Saccharomvces cerevisiae and<br />
Schizosaccharomvces pombe chromosomes were used as<br />
molecular size markers. Although strain ATCC 16601 and<br />
strain ATCC 9990 had such different chromosome patterns,<br />
chromosomal banding pattern <strong>of</strong> fusants were identical to<br />
parental strains.<br />
J.THOMAS MULLINS. Department <strong>of</strong> Botany,<br />
University <strong>of</strong> Florida. Gainesville, FL<br />
32611. Structure and function <strong>of</strong> soluble<br />
cytoplasmic beta-glucans in Achlve.<br />
Water-soluble beta-glucans are major<br />
cytoplasmic constituents <strong>of</strong> Achlve. Two<br />
forms <strong>of</strong> these glucans were found, a<br />
neutral type (18%) and an acidic<br />
phosphorylated type (82%). Both forms<br />
release only glucose on hydrolysis, and<br />
the polymer is formed by beta-glucosidic<br />
linkages. These glucans function as<br />
carbon, and probably phosphorus, reserves<br />
in the mycelium, that support sexual and<br />
asexual reproductive cycles during<br />
staravation conditions. At least one<br />
beta-glucanase can be demonstrated in the<br />
mycelium, which is capable <strong>of</strong> hydrolyzing<br />
these glucans.<br />
MELANI K. OAKLEY. DAVID E. LEMKE and ROBEm D.<br />
KOEHN. Department <strong>of</strong> Biology. Southwest Texas State Uni-<br />
versity. San Marcos. TX 78666 -- Endomycorrhizal inoculum<br />
potential <strong>of</strong> surface mined lands: A bioassay <strong>of</strong> different aged<br />
sites.<br />
Mycorrhfzal inoculum potential IMIP) <strong>of</strong> a site has been<br />
recognized as an important factor in the reclamation <strong>of</strong> surface<br />
mined lands. Successful revegetation efforts may well<br />
hinge on the amount <strong>of</strong> V-A mycorrhizal inoculum present.<br />
After d~sturbance. an unknown penod <strong>of</strong> time must elapse<br />
before the MIP reacnes its pre-disturbance level. At a lignite<br />
mine m central Texas. spoils varying in age from 0-35 years<br />
were sampled, as was soil from an adjacent. undisturbed area<br />
<strong>of</strong> the mine. These samples were anaiyzed for nurrient availa-<br />
bility and pH. and bioassayed to determine the MIP for each<br />
site. The bioassay was conducted uslng corn seedlings grown<br />
in undiluted soil. as well as in soil dilutions <strong>of</strong> 1:4 and 1:40.<br />
and undiluted sterilized soil. Roots were harvested after<br />
periods <strong>of</strong> 30. 60. and 90 days and examined for the presence<br />
<strong>of</strong> V-A mycorrhizal fungi. The MIP <strong>of</strong> the undisturbed soil<br />
was greater than 50 percent, while that <strong>of</strong> the other sites de-<br />
clined in proportion to their ages.<br />
L. A. O'GORHAN, E. W. ROBINS. J. HAN, R. GUPTA and<br />
H. E. BROCKMAN. Department <strong>of</strong> Biological Sciences,<br />
Illinois State University, Normal, IL 61761.<br />
Viability <strong>of</strong> ad-3 mutant conidia <strong>of</strong> Neurospora<br />
crassa in pH 7 media.<br />
We use plates <strong>of</strong> Westergaard's basal medium<br />
supplemented with calcium pantothenate, casamino<br />
acids, a mixture <strong>of</strong> vitamins, a trace (0.1 uglml) <strong>of</strong><br />
adenine sulfate, and 1% sucrose (reversion medium)<br />
for assaying the reversion <strong>of</strong> ad-3 mutants <strong>of</strong><br />
Neurospora crassa carrying pan-2 and cot-l (causes<br />
colonial growth) markers. Plates <strong>of</strong> the same medium<br />
supplemented with 25 ug <strong>of</strong> adenine sulfate/ml<br />
(survival medium) are used for measuring conidial<br />
viability in the reversion experiments. We noted<br />
low conidial viability (~5%) when the survival<br />
medium was adjusted to pH 7, but not to pH 5 or 6.<br />
This low viability at pH 7 was not observed with<br />
another plating medium (Fries' basal medium<br />
supplemented with calcium pantothenate, 100 ug <strong>of</strong><br />
adenine sulfate/ml, and 0.52 each <strong>of</strong> fructose and<br />
glucose). Data will be presented showing that the low<br />
viability in the survival medium at pH 7 is not due<br />
to the difference in adenine sulfate concentration<br />
or the presence <strong>of</strong> casamino acids or the mixture <strong>of</strong><br />
vitamins, but is due to the presence <strong>of</strong> sucrose<br />
rather than fructose and glucose. When the standard<br />
2 X lo7 conidialplate from each <strong>of</strong> 2 ad-3 mutants<br />
were used on plates <strong>of</strong> the reversion medium, the<br />
spontaneous reversion frequency was about the same<br />
at pH 6, 7, and 8. We conclude that the decrease<br />
in viability <strong>of</strong> conidia from ad-3 mutants <strong>of</strong><br />
-- N. crassa in pH 7 media is dependent on carbon<br />
source and conidial concentration.<br />
W. J. OTROSINA. T. E. CHASE. F. W. COBB, JR.. and K.<br />
KORHONEN. USDA Forest Service. 1960 Addison Street,<br />
Berkeley. CA. 94701; University <strong>of</strong> California.<br />
Department <strong>of</strong> Plant Pathology. Berkeley. CA, 94704;<br />
and Finnish Forest Research Insititute. Helsinki.<br />
Finland.<br />
Allozyme comparisons between intersterility groups <strong>of</strong><br />
North <strong>America</strong>n and European Heterobasidion annosum.<br />
Allozyme analyses were conducted for S, and P<br />
intersterility (IS) groups <strong>of</strong> H. annosum from Europe<br />
and western North <strong>America</strong>. Eleven enzyme systems and<br />
13 loci were resolved. Very few alleles were shared<br />
between IS groups from western North <strong>America</strong>.<br />
indicating a large degree <strong>of</strong> genetic divergence and<br />
lack <strong>of</strong> gene flow between them. Several loci such as<br />
alcohol dehydrogenase, aconitase, and malate<br />
dehydrogenase were virtually fixed for alternative<br />
alleles between the two biological species and could