Fan Xu, Gong Ting, Wu Yunbo, Zhao Fengjie, Qiao Mingqiang, Wang Shufang, Yang Chao
1Key Laboratory of Molecular Microbiology and Technology for Ministry of Education, Department of Microbiology, Nankai University, Tianjin, 300071 China.
2State Key Laboratory of Medicinal Chemical Biology and College of Life Sciences, Nankai University, Tianjin, 300071 China.
3 Biotech. 2019 Sep;9(9):344. doi: 10.1007/s13205-019-1873-7. Epub 2019 Aug 24.
This study aimed to investigate the effects of cytoskeleton protein MreB on bacterial cell morphology and the synthesis of alginate oligosaccharides (AO) and polyhydroxyalkanoate (PHA) by NK-01. To overexpress the gene, an expression vector encoding MreB-GFP fusion protein was constructed. The scanning electron microscope (SEM) showed that cells expressing MreB were longer than the wild ones, which agrees with MreB's relationship with the synthesis of peptidoglycan. Cells expressing the MreB-GFP fusion protein emitted green fluorescence under a fluorescence microscope, suggesting that MreB was functionally expressed in strain NK-01. Under a confocal laser scanning microscope, MreB was observed as located around the cell membrane. Furthermore, the recombinant strain could synthesize 0.961 g/L AO, which was 5.86-fold higher than wild-type strain. Through the medium optimization test, we finally selected the addition of 20 g/L glucose as the optimal glycogen addition for AO fermentation based on a high AO yield and high substrate transformation efficiency. The results indicated that overexpression of MreB affected the cell morphology, the activity of AO polymerase, and the efficiency of AO secretion. However, the synthesis of PHA for recombinant strain was slightly reduced. The results suggested that the overexpression of this cytoskeleton protein affected the yield of specific intracellular and extracellular products.
本研究旨在探究细胞骨架蛋白MreB对细菌细胞形态以及NK-01合成藻酸寡糖(AO)和聚羟基脂肪酸酯(PHA)的影响。为使该基因过表达,构建了编码MreB-GFP融合蛋白的表达载体。扫描电子显微镜(SEM)显示,表达MreB的细胞比野生型细胞更长,这与MreB与肽聚糖合成的关系相符。在荧光显微镜下,表达MreB-GFP融合蛋白的细胞发出绿色荧光,表明MreB在菌株NK-01中实现了功能性表达。在共聚焦激光扫描显微镜下,观察到MreB位于细胞膜周围。此外,重组菌株能够合成0.961 g/L的AO,比野生型菌株高出5.86倍。通过培养基优化试验,基于高AO产量和高底物转化效率,我们最终选择添加20 g/L葡萄糖作为AO发酵的最佳糖原添加量。结果表明,MreB的过表达影响了细胞形态、AO聚合酶活性和AO分泌效率。然而,重组菌株的PHA合成略有减少。结果表明,这种细胞骨架蛋白的过表达影响了特定细胞内和细胞外产物的产量。