摘要
用5%麦粉的α-淀粉酶水解液培养麦角菌ATCC20019,结果其发酵液能产生麦角隐亭(50.16±2.40)μg/mL,与30%蔗糖的发酵培养基的产碱量(20.74±3.53)μg/mL相比,两者有差异(p<0.05).在10%蔗糖的培养基中,发酵第4天后补加5%麦粉的α-淀粉酶水解液,麦角隐亭的产量为(47.12±6.34)μg/mL,也高于碳源为30%蔗糖的产碱量(19.89±2.40)μg/mL,两者差异显著,p<0.01.而两种方法的菌丝体生长量均相差无几,p>0.05.
Claviceps purpurea ATCC 20019 could produce ergocryptine 50. 16±2. 40μg/mL in the fermentative medium containing α-hydrolyzate of 5% wheat flour, but the alkaioid yield was 20.74±3. 53μg/mL in the fermentative medium containing 30% sucrose. There was difference between the two, p<0. 05. After 4 days fermentation in medium containing 10% sucrose,hydrolyzate of 5% wheat flour was supplemented. The yield of ergocryptine 47.12±6. 34μg/mLwas higher than that of 30% sucrose 19. 89±2. 40μg/mL, p<0. 01. There was no obvious difference between the mycelia biomasses of the two methods, p>0. 05.
出处
《上海师范大学学报(自然科学版)》
1996年第1期65-69,共5页
Journal of Shanghai Normal University(Natural Sciences)
关键词
麦角菌
发酵培养
碳源
α-淀粉酶水解液
Claviceps purpurea
fermentation
carbon source
α-amylase hydrolyzate