Makhmud S A, Mashkhur V A, El'-Khaddad M E, El'Gammal S E
Mikrobiologiia. 1978 Mar-Apr;47(2):220-5.
The optimal conditions for biosynthesis of exocellular glucoamylase were found in the course of submerged cultivation of Aspergillus foetidus ATCC 14916: pH 4.5 at the beginning of cultivation, cultivation for four days, a temperature of 30 degrees C, and an aeration in the fermenter of 1.5 volumes of the air per 1 volume of the medium with a stirring of 280 rpm. The material can be inoculated either as spores (1 X 10(7) spores per 100 ml of the medium) or a material germinated from spores (5% by volume). The composition of the medium was improved by using waste products of the agricultural industry (wheat and rice bran, yellow maize, etc.). The maximum biosynthesis of glucoamylase under the optimum conditions of cultivation was observed on crushed yellow maize (10--15%): up to 6.8--8.0 units of GIA (g of glucose per hour) per 1 ml of the cultural filtrate which was 3.4--4.0 times higher than on the original medium and 5--10 times higher than for Endomycopsis bispora, Endomycopsis sp. 20--9, Aspergillus niger and other cultures producing glucoamylase.
在泡盛曲霉ATCC 14916的深层培养过程中,发现了胞外糖化酶生物合成的最佳条件:培养开始时pH值为4.5,培养4天,温度为30℃,发酵罐中的通气量为每1体积培养基1.5体积空气,搅拌速度为280转/分钟。接种材料可以是孢子(每100毫升培养基1×10⁷个孢子)或由孢子萌发的材料(体积比5%)。通过使用农业工业废料(麦麸、米糠、黄玉米等)改进了培养基的成分。在最佳培养条件下,在粉碎的黄玉米(10 - 15%)上观察到糖化酶的最大生物合成:每1毫升培养滤液高达6.8 - 8.0单位的GIA(每小时克葡萄糖),这比原始培养基高3.4 - 4.0倍,比双孢内孢霉、内孢霉属20 - 9、黑曲霉和其他产生糖化酶的培养物高5 - 10倍。