McCarthy P J, Troke P F, Gull K
J Gen Microbiol. 1985 Apr;131(4):775-80. doi: 10.1099/00221287-131-4-775.
Nikkomycin was found to be a potent growth inhibitor of Candida albicans through competitive inhibition of chitin synthase [Ki = 0.16 microM (0.1 microgram ml-1)]. The activity of the peptide-nucleoside drug was antagonized by both peptone and defined peptides. Transported dipeptides were effective antagonists while transported oligopeptides were not. A mutant of C. albicans resistant to the effects of nikkomycin through a transport defect was unable to transport dipeptides, while oligopeptide uptake was apparently unaffected. At least two peptide permeases are operational in this organism.
通过对几丁质合成酶的竞争性抑制作用(Ki = 0.16微摩尔/升(0.1微克/毫升)),发现多氧霉素是白色念珠菌的一种有效生长抑制剂。蛋白胨和特定肽均能拮抗这种肽 - 核苷药物的活性。转运的二肽是有效的拮抗剂,而转运的寡肽则不是。白色念珠菌中通过转运缺陷而对多氧霉素作用产生抗性的一个突变体无法转运二肽,而寡肽摄取显然未受影响。该生物体中至少有两种肽通透酶在起作用。