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首页> 外文期刊>Applied and Environmental Microbiology >Heterologous Expression of Lactose- and Galactose-Utilizing Pathways from Lactic Acid Bacteria in Corynebacterium glutamicum for Production of Lysine in Whey
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Heterologous Expression of Lactose- and Galactose-Utilizing Pathways from Lactic Acid Bacteria in Corynebacterium glutamicum for Production of Lysine in Whey

机译:谷氨酸棒杆菌生产乳清中赖氨酸的乳酸菌中乳糖和半乳糖利用途径的异源表达

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The genetic determinants for lactose utilization from Lactobacillus delbrueckii subsp. bulgaricus ATCC 11842 and galactose utilization from Lactococcus lactis subsp. cremoris MG 1363 were heterologously expressed in the lysine-overproducing strain Corynebacterium glutamicum ATCC 21253. The C. glutamicum strains expressing the lactose permease and β-galactosidase genes of L. delbrueckii subsp. bulgaricus exhibited β-galactosidase activity in excess of 1,000 Miller units/ml of cells and were able to grow in medium in which lactose was the sole carbon source. Similarly, C. glutamicum strains containing the lactococcal aldose-1-epimerase, galactokinase, UDP-glucose-1-P-uridylyltransferase, and UDP-galactose-4-epimerase genes in association with the lactose permease and β-galactosidase genes exhibited β-galactosidase levels in excess of 730 Miller units/ml of cells and were able to grow in medium in which galactose was the sole carbon source. When grown in whey-based medium, the engineered C. glutamicum strain produced lysine at concentrations of up to 2 mg/ml, which represented a 10-fold increase over the results obtained with the lactose- and galactose-negative control, C. glutamicum 21253. Despite their increased catabolic flexibility, however, the modified corynebacteria exhibited slower growth rates and plasmid instability.
机译:德姆乳杆菌亚种中乳糖利用的遗传决定因素。 bulgaricus ATCC 11842和 Lactococcus lactis 亚种中半乳糖的利用。 cremoris MG 1363在赖氨酸过量生产菌株谷氨酸棒杆菌 ATCC 21253中异源表达。表达 L的乳糖通透酶和β-半乳糖苷酶基因的谷氨酸菌株。 delbrueckii 子空间 bulgaricus 的β-半乳糖苷酶活性超过1000 Miller单位/ ml细胞,并且能够在以乳糖为唯一碳源的培养基中生长。同样, C。含有乳酸球菌醛糖1-表皮酶,半乳糖激酶,UDP-葡萄糖-1-P-尿苷转移酶和UDP-半乳糖4-表皮酶基因以及乳糖通透酶和β-半乳糖苷酶基因的谷氨酸菌株表现出β-半乳糖苷酶水平超过730 Miller单位/ ml细胞,并且能够在半乳糖为唯一碳源的培养基中生长。在基于乳清的培养基中生长时,工程化的 C。谷氨酸菌株产生的赖氨酸浓度最高为2 mg / ml,比乳糖和半乳糖阴性对照 C的结果高10倍。谷氨酸21253。尽管它们具有更高的分解代谢灵活性,但修饰的棒状杆菌却显示出较慢的生长速率和质粒不稳定性。

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