减压
食品科学
突变体
生物化学
糖
藤条
拉伤
化学
酶
生物
生物技术
基因
心理压抑
基因表达
解剖
作者
Shuhang Zhang,Hong Jiang,Si‐Jia Xue,Na Ge,Yi Sun,Zhe Chi,Guang-Lei Liu,Zhen‐Ming Chi
标识
DOI:10.1021/acs.jafc.9b05826
摘要
Fructooligosaccharides (FOSs) are excellent food ingredients or feed additives by stimulating probiotics. In this paper, a CREA gene encoding a glucose repressor in the β-fructofuranosidase producer Aureobasidium melanogenum 33 with high-level FOS biosynthesis was disrupted, and glucose repression in disruptant D28 was relieved. The disruptant D28 produced up to 2100 U/mL of β-fructofuranosidase activity, whereas the enzyme activities produced by parent strain 33 and complemented strain C11 were below 600 U/mL. The whole cells of the disruptant D28 was used to convert cane molasses into FOSs, and 0.58 g of FOSs/g of molasses sugar was synthesized from 350 g/L cane molasses sugar within 4 h. Results demonstrated that the industrial waste cane molasses can be efficiently converted into FOSs by the glucose derepression mutant D28 with high β-fructofuranosidase activity. This low-cost and environmentally friendly bioprocess has great potential applications in bioengineering and biotechnology for FOS production.
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