Santos T, Sánchez M, Villanueva J R, Nombela C
J Bacteriol. 1979 Jan;137(1):6-12. doi: 10.1128/jb.137.1.6-12.1979.
The localization of the derepressible beta-1,3-glucanases of Penicillium italicum and the cell wall autolysis under conditions of beta-1,3-glucanase derepression (24 h in a low-glucose medium) were studied. About 15% of the total activity was secreted into the culture medium during the 24-h period and consisted of similar amounts of each of the three beta-1,3-glucanases (I, II, III) produced by this species. Treatment of derepressed mycelia with periplasmic enzyme-inactivating agents resulted in a loss of 45% of the mycelium-bound beta-1,3-glucanase. Analysis of periplasmic enzymes solubilized by 2 M NaCl or by autolysis of isolated cell walls revealed that only beta-1,3-glucanases II and III were bound to the cell wall. These two enzymes were capable of releasing in vitro reducing sugars from cell walls, whereas beta-1,3-glucanase I was not. In addition, the autolytic activity of cell walls isolated from derepressed mycelium was greater than that of cell walls isolated from repressed mycelium. The incubation of the fungus in the low-glucose medium also resulted in the in vivo mobilization of 34% of the cell wall beta-1,3-glucan, and this mobilization was fully prevented by cycloheximide, which also blocked derepression of beta-1,3-glucanases. Derepression of beta-1,3-glucanase seems to be coupled to the mobilization of cell wall glucan.
研究了意大利青霉可去阻遏β-1,3-葡聚糖酶的定位以及在β-1,3-葡聚糖酶去阻遏条件下(在低葡萄糖培养基中培养24小时)的细胞壁自溶情况。在24小时内,约15%的总活性分泌到培养基中,且由该菌种产生的三种β-1,3-葡聚糖酶(I、II、III)各占相似的量。用周质酶失活剂处理去阻遏的菌丝体会导致45%与菌丝体结合的β-1,3-葡聚糖酶丧失。对用2M NaCl溶解或通过分离细胞壁自溶得到的周质酶进行分析表明,只有β-1,3-葡聚糖酶II和III与细胞壁结合。这两种酶能够在体外从细胞壁释放还原糖,而β-1,3-葡聚糖酶I则不能。此外,从去阻遏菌丝体分离得到的细胞壁的自溶活性大于从阻遏菌丝体分离得到的细胞壁。在低葡萄糖培养基中培养该真菌还导致34%的细胞壁β-1,3-葡聚糖在体内被动员,而环己酰亚胺完全阻止了这种动员,环己酰亚胺也阻断了β-1,3-葡聚糖酶的去阻遏。β-1,3-葡聚糖酶的去阻遏似乎与细胞壁葡聚糖的动员相关。