Asano N, Yamaguchi T, Kameda Y, Matsui K
J Antibiot (Tokyo). 1987 Apr;40(4):526-32. doi: 10.7164/antibiotics.40.526.
The pseudo-oligosaccharides, validamycins, showed potent inhibitory activity against trehalase of Rhizoctonia solani while no significant inhibition was exhibited against cellulase, pectinase, chitinase, alpha-amylase, alpha- and beta-glucosidases. In particular, validoxylamine A strongly inhibited trehalase in a competitive manner with a Ki value of 1.9 X 10(-9) M. The uptake of the antibiotic into the cell and the amount of the intracellular trehalose were investigated by incubating the washed mycelia of R. solani with validamycins. It was found that validamycin A is transported into the cell and hydrolyzed therein by a beta-glucosidase yielding validoxylamine A with greater inhibitory activity. Also validamycin A containing beta-D-glucosyl residue is more favorably taken up into the cell than validamycin D containing alpha-D-glucosyl residue or their common aglycone, validoxylamine A. In addition, validamycin A suppressed the in vivo degradation of the intracellular trehalose at very low concentration of 0.1 microgram/ml.
假寡糖井冈霉素对茄丝核菌的海藻糖酶表现出强大的抑制活性,而对纤维素酶、果胶酶、几丁质酶、α淀粉酶、α和β糖苷酶未表现出明显抑制作用。特别是,井冈霉胺A以竞争性方式强烈抑制海藻糖酶,其抑制常数Ki值为1.9×10(-9)M。通过用井冈霉素孵育茄丝核菌洗涤后的菌丝体,研究了抗生素进入细胞的情况以及细胞内海藻糖的含量。发现井冈霉素A被转运到细胞中,并在其中被β糖苷酶水解,产生具有更强抑制活性的井冈霉胺A。此外,含有β-D-葡萄糖基残基的井冈霉素A比含有α-D-葡萄糖基残基的井冈霉素D或它们的共同糖苷配基井冈霉胺A更易被细胞摄取。另外,井冈霉素A在0.1微克/毫升的极低浓度下就能抑制细胞内海藻糖的体内降解。