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Functional Analysis of the Lactococcus lactis galU and galE Genes and Their Impact on Sugar Nucleotide and Exopolysaccharide Biosynthesis

机译:乳酸乳球菌galU和galE基因的功能分析及其对糖核苷酸和胞外多糖生物合成的影响

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摘要

We studied the UDP-glucose pyrophosphorylase (galU) and UDP-galactose epimerase (galE) genes of Lactococcus lactis MG1363 to investigate their involvement in biosynthesis of UDP-glucose and UDP-galactose, which are precursors of glucose- and galactose-containing exopolysaccharides (EPS) in L. lactis. The lactococcal galU gene was identified by a PCR approach using degenerate primers and was found by Northern blot analysis to be transcribed in a monocistronic RNA. The L. lactis galU gene could complement an Escherichia coli galU mutant, and overexpression of this gene in L. lactis under control of the inducible nisA promoter resulted in a 20-fold increase in GalU activity. Remarkably, this resulted in approximately eightfold increases in the levels of both UDP-glucose and UDP-galactose. This indicated that the endogenous GalE activity is not limiting and that the GalU activity level in wild-type cells controls the biosynthesis of intracellular UDP-glucose and UDP-galactose. The increased GalU activity did not significantly increase NIZO B40 EPS production. Disruption of the galE gene resulted in poor growth, undetectable intracellular levels of UDP-galactose, and elimination of EPS production in strain NIZO B40 when cells were grown in media with glucose as the sole carbon source. Addition of galactose restored wild-type growth in the galE disruption mutant, while the level of EPS production was approximately one-half the wild-type level.
机译:我们研究了乳酸乳球菌MG1363的UDP-葡萄糖焦磷酸化酶(galU)和UDP-半乳糖差向异构酶(galE)基因,以研究它们参与UDP-葡萄糖和UDP-半乳糖的生物合成,UDP-葡萄糖和UDP-半乳糖是含葡萄糖和半乳糖的外多糖(乳酸乳球菌。通过使用简并引物的PCR方法鉴定了乳球菌galU基因,并通过Northern印迹分析发现其在单顺反子RNA中转录。乳酸乳球菌galU基因可以补充大肠杆菌galU突变体,该基因在可诱导的nisA启动子控制下在乳酸乳球菌中的过表达导致GalU活性增加20倍。显着地,这导致UDP-葡萄糖和UDP-半乳糖的水平都增加了大约八倍。这表明内源性GalE活性不受限制,并且野生型细胞中的GalU活性水平控制着细胞内UDP-葡萄糖和UDP-半乳糖的生物合成。 GalU活性的增加并未显着增加NIZO B40 EPS的产量。当细胞在以葡萄糖为唯一碳源的培养基中生长时,galE基因的破坏导致生长不良,细胞内UDP半乳糖水平无法检测到,并且消除了NIZO B40菌株中的EPS产生。半乳糖的添加恢复了galE破坏突变体中的野生型生长,而EPS产生的水平约为野生型水平的一半。

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