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1.
Curr Genet ; 32(3): 237-43, 1997 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-9339350

RESUMO

Sequence analysis of the rDNA region containing the internal transcribed spacer (ITS) regions and the 5.8s rDNA coding sequence was used to evaluate the genetic diversity of 45 isolates within and between anastomosis groups (AGs) in Rhizoctonia solani. The 5.8s rDNA sequence was completely conserved across all the AGs examined, whereas the ITS rDNA sequence was found to be highly variable among isolates. The sequence homology in the ITS regions was above 96% for isolates of the same subgroup, 66-100% for isolates of different subgroups within an AG, and 55-96% for isolates of different AGs. In neighbor-joining trees based on distances derived from ITS-5.8s rDNA sequences, subgroups IA, IB and IC within AG-1 and subgroups HG-I and HG-II within AG-4 were placed on statistically significant branches as assessed by bootstrap analysis. These results suggest that sequence analysis of ITS rDNA regions of R. solani may be a valuable tool for identifying AG subgroups of biological significance.


Assuntos
DNA Ribossômico , Rhizoctonia/genética , Sequência de Bases , Heterogeneidade Genética , Variação Genética
2.
Biol Pharm Bull ; 16(7): 698-701, 1993 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-8401405

RESUMO

Nineteen isoflavones were synthesized and their attracting activity to Aphanomyces euteiches zoospore were investigated. Isoflavones (1, 2, 4, 16 and 19) with an unsubstituted B ring were synthesized by the oxidation of corresponding 2'-hydroxychalcones with thallium (III) nitrate trihydrate in methanolic perchloric acid. A hydroxyl group at the C-5 position in isoflavones was necessary for strong attraction to A. euteiches zoospore. The introduction of an additional hydroxyl group at the C-7 or C-4' position strengthened the attracting activity. Moreover, the methylation of the C-7 hydroxyl group strengthened the attracting activity, but the methylation of the C-4' hydroxyl group slightly weakened it. The naturally occurring isoflavones (9 and 10), which were reported to possess estrogen activity, showed moderate attracting activity.


Assuntos
Chalcona/química , Isoflavonas/síntese química , Oomicetos/efeitos dos fármacos , Isoflavonas/química , Isoflavonas/farmacologia , Metilação , Oomicetos/fisiologia , Oxirredução , Esporos Fúngicos/efeitos dos fármacos , Esporos Fúngicos/fisiologia
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