Benallaoua S, Bellal M, Bonaly R
Institut de biologie, Centre universitaire de Bejaia, Algérie.
Can J Microbiol. 1995 Aug;41(8):722-9.
The desertomycin action upon Saccharomyces uvarum wall synthesis has been studied. Spheroblast regeneration was carried out in a liquid medium containing labeled glucose to monitor the synthesis of different wall components. In the presence of desertomycin, wall synthesis was affected; this was expressed as a net reduction of insoluble alkali constituents content, more precisely the insoluble acido-alkali fraction that, in yeasts, is constituted by chains of beta(1,3)-glucans linked among themselves by beta(1,6) bonds. Mannan formation was not inhibited such polymers that cannot be fixed to the glucan matrix of the wall were liberated in the regeneration medium. Because of desertomycin action, the decrease in insoluble alkali content revealed an interference with the enzymatic systems catalyzing glucan synthesis. In vitro, however, this antifungal had little effect upon glucan synthetase activity: doses 5 times superior to the subinhibiting level used in vivo caused only 30% inhibition. This result can be explained by an indirect action of desertomycin. Parietal disorders were the result of membrane structure disturbance, notably the phospholipids and localized enzymatic systems. This antifungal presents an analogical structure with macrolides with recognized membrane action.
已对去甲金霉素对葡萄汁酵母细胞壁合成的作用进行了研究。在含有标记葡萄糖的液体培养基中进行原生质球再生,以监测不同细胞壁成分的合成。在去甲金霉素存在的情况下,细胞壁合成受到影响;这表现为不溶性碱成分含量的净减少,更确切地说是不溶性酸碱部分,在酵母中,它由通过β(1,6)键相互连接的β(1,3)-葡聚糖链组成。甘露聚糖的形成未受抑制,那些无法固定在细胞壁葡聚糖基质上的聚合物在再生培养基中被释放出来。由于去甲金霉素的作用,不溶性碱含量的降低表明其对催化葡聚糖合成的酶系统产生了干扰。然而,在体外,这种抗真菌剂对葡聚糖合成酶活性影响很小:比体内使用的亚抑制水平高5倍的剂量仅导致30%的抑制。这一结果可以通过去甲金霉素的间接作用来解释。细胞壁紊乱是膜结构紊乱的结果,特别是磷脂和局部酶系统。这种抗真菌剂与具有公认膜作用的大环内酯类具有类似结构。