EVIDENCE FOR SELECTIVE SULFHYDRYL REACTIVITY IN CYTOCHALASIN-A - MEDIATED BACTERIAL INHIBITIONS

被引:9
作者
CUNNINGHAM, D
FLASHNER, M
TANENBAUM, SW
机构
[1] Department of Chemistry, SUNY College of Environmental Science and Forestry, Syracuse
关键词
D O I
10.1016/0006-291X(79)90397-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cytochalasin A (CA) at 5 × 10-5 M strongly inhibits glucose transport in Arthrobacter sialophilis. This effect and other bacteriostatic and metabolic inhibitions of gram-positive bacteria are not caused by the closely related congeners cytochalasin B or D. Inhibitions by CA are nullified by prior drug incubation with sulfhydryl compounds. It was also found that the characterized adduct of CA with β-mercaptoethanol is devoid of biological activity. N-ethylmaleimide, p-chloromercuribenzoate and ethacrynic acid (a known, liposoluble, sulfhydryl reactant) were each shown at 5 × 10-5 M to be relatively ineffective in inhibiting D-glucose transport in A. sialophilus. These observations suggest that CA reacts at the molecular biological level in a site-specific manner. © 1979.
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页码:173 / 179
页数:7
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