| Abstract: | Studies were carried out to test the possibility of identifying European Armillaria species by using isozyme patterns. Twenty-two different enzymes were used to analyse the haploid and diploid mycelium extract of Armillaria borealis, Armillaria cepistipes, Armillaria gallica, Armillaria mellea, Armillaria ostoyae and Armillaria tahescens. Tests for fumarase (E.C. 4.2.1.1.), aconitase (E.C. 4.2.1.3.), leucine-amino peptidase (E.C. 3.4.11.1.), isocitrate dehydrogenase (E.C. 1.1.1.42.), shikimic dehydrogenase (E.C. 1.1.1.25), glucose-6-P-dehydrogenase (E.C. 1.1.1.49.), malic enzyme (E.C. 1.1.1.40.), 6-P-gluconic dehydrogenase (E.C. 1.1.4.4.), pectin esterase (E.C. 3.1.1.11.), and pectic lyase (E.C. 4.2.99.3.) did not reveal enzyme activity. Isozyme profiles of acid phosphatase (E.C. 3.1.3.2.), phospho-gluco-isomerase (E.C. 5.3.1.9.), peroxidase (E.C. 1.11.1.7.), polyphenoloxidase (E.C. 1.14.18.), malic dehydrogenase (E.C. 1.1.1.37.), glutamic dehydrogenase (E.C. 1.4.1.3.) and superoxide dismutase (E.C. 1.15.1.1.) were ineffective for species identification. In contrast, esterase (E.C. 3.1.1.1.), glutamic-oxalacetic transaminase (2.6.1.1.), phospho-gluco-mutase (E.C. 2.7.5.1.), alcohol dehydrogenase (E.C. 1.1.1.1.), and polygalacturonase (E.C. 3.2.1.15.) isoenzyme patterns showed enough polymorphism to allow the identification of the different Armillaria species. However, it is necessary to compare several enzyme profiles for a conclusive identification. Intraspecific crosses of A tabescens were confirmed by the presence of a heteromeric isozyme pattern of alcohol dehydrogenase and phospho-gluco-mutase. |
