Albert H, Davies D J, Woodson L P, Soper C J
School of Pharmacy and Pharmacology, University of Bath, UK.
J Appl Microbiol. 1998 Nov;85(5):865-74. doi: 10.1046/j.1365-2672.1998.00607.x.
The alpha-glucosidase enzyme was isolated from vegetative cells and spores of Bacillus stearothermophilus, ATCC 7953. Spore-associated enzyme had a molecular weight of approximately 92,700, a temperature optimum of 60 degrees C, and a pH optimum of 7.0-7.5. The enzyme in crude aqueous spore extract was stable for 30 min up to a temperature of 65 degrees C, above which the enzyme was rapidly denatured. The optimal pH for stability of the enzyme was approximately 7.2. The alpha-glucosidase in crude vegetative cell extract had similar characteristics to the spore-associated enzyme but its molecular weight was 86,700. The vegetative cell and spore-associated enzymes were cross-reactive. The enzymes are postulated to derive from a single gene product, which undergoes modification to produce the spore-associated form. The location of alpha-glucosidase in the spore coats (outside the spore protoplast) is consistent with the location of most enzymes involved in activation, germination and outgrowth.
α-葡萄糖苷酶是从嗜热脂肪芽孢杆菌(ATCC 7953)的营养细胞和孢子中分离出来的。与孢子相关的酶分子量约为92,700,最适温度为60℃,最适pH为7.0 - 7.5。粗制孢子水提取物中的酶在高达65℃的温度下可稳定30分钟,超过该温度酶会迅速变性。酶稳定性的最适pH约为7.2。粗制营养细胞提取物中的α-葡萄糖苷酶与孢子相关的酶具有相似的特性,但其分子量为86,700。营养细胞和孢子相关的酶具有交叉反应性。推测这些酶源自单一基因产物,该产物经过修饰后产生与孢子相关的形式。α-葡萄糖苷酶在孢子壁(孢子原生质体外)中的位置与大多数参与激活、萌发和生长的酶的位置一致。