Santos T, Villanueva J R, Nombela C
J Bacteriol. 1977 Jan;129(1):52-8. doi: 10.1128/jb.129.1.52-58.1977.
The filamentous fungus Penicillium italicum, grown in a defined liquid medium, produced beta-1,3-glucanase, which remained essentially bound to the cells, and beta-1,6-glucanase, an essentially extracellular enzyme. When glucose was depleted from the medium, when a limited concentration of glucose (0.2%) was maintained, or when the carbon source was galactose (3%) or lactose (3%), a significant increase in the specific activity of beta-1,3-glucanase, in cell extracts, took place. This was paralleled by a very slow rate of growth, and under glucose limitation, the appearance of beta-1,3-glucanase in the medium was also observed. On the other hand, when an excess of glucose, fructose, or sucrose was present, the specific activity remained constant and active growth was promoted. Laminarin, cellobiose, gentiobiose, and isolated Penicillium italicum walls were not capable of significantly inducing beta-1,3-glucanase synthesis to a level beyond that attained by glucose limitation. A similar behavior was observed for beta-1,6-glucanase. beta-1,3-Glucanase and beta-1,6-glucanase are therefore constitutive enzymes subjected to catabolite repression. The results are discussed in the context of the possible functions that have been suggested for glucanases and related enzymes.
在特定液体培养基中生长的丝状真菌意大利青霉可产生β-1,3-葡聚糖酶(该酶基本与细胞结合)和β-1,6-葡聚糖酶(一种基本为胞外酶)。当培养基中的葡萄糖耗尽时,当维持有限浓度的葡萄糖(0.2%)时,或者当碳源为半乳糖(3%)或乳糖(3%)时,细胞提取物中β-1,3-葡聚糖酶的比活性显著增加。这伴随着非常缓慢的生长速率,并且在葡萄糖受限的情况下,还观察到培养基中出现β-1,3-葡聚糖酶。另一方面,当存在过量的葡萄糖、果糖或蔗糖时,比活性保持恒定并促进了活跃生长。海带多糖、纤维二糖、龙胆二糖和分离的意大利青霉细胞壁不能显著诱导β-1,3-葡聚糖酶的合成,使其水平超过葡萄糖受限所达到的水平。β-1,6-葡聚糖酶也观察到类似的行为。因此,β-1,3-葡聚糖酶和β-1,6-葡聚糖酶是受分解代谢物阻遏的组成型酶。在已提出的葡聚糖酶和相关酶的可能功能的背景下讨论了这些结果。