Smith L T, Pocard J A, Bernard T, Le Rudulier D
Plant Growth Laboratory, University of California, Davis 95616.
J Bacteriol. 1988 Jul;170(7):3142-9. doi: 10.1128/jb.170.7.3142-3149.1988.
Intracellular accumulation of glycine betaine has been shown to confer an enhanced level of osmotic stress tolerance in Rhizobium meliloti. In this study, we used a physiological approach to investigate the mechanism by which glycine betaine is accumulated in osmotically stressed R. meliloti. Results from growth experiments, 14C labeling of intermediates, and enzyme activity assays are presented. The results provide evidence for the pathway of biosynthesis and degradation of glycine betaine and the osmotic effects on this pathway. High osmolarity in the medium decreased the activities of the enzymes involved in the degradation of glycine betaine but not those of enzymes that lead to its biosynthesis from choline. Thus, the concentration of the osmoprotectant glycine betaine is increased in stressed cells. This report demonstrates the ability of the osmolarity of the growth medium to regulate the use of glycine betaine as a carbon and nitrogen source or as an osmoprotectant. The mechanisms of osmoregulation in R. meliloti and Escherichia coli are compared.
已证明甘氨酸甜菜碱在细胞内积累可使苜蓿根瘤菌的渗透胁迫耐受性增强。在本研究中,我们采用生理学方法来研究甘氨酸甜菜碱在渗透胁迫下的苜蓿根瘤菌中积累的机制。文中给出了生长实验、中间体的¹⁴C标记以及酶活性测定的结果。这些结果为甘氨酸甜菜碱的生物合成和降解途径以及渗透对该途径的影响提供了证据。培养基中的高渗透压降低了参与甘氨酸甜菜碱降解的酶的活性,但未降低由胆碱合成甘氨酸甜菜碱的酶的活性。因此,在受胁迫的细胞中,渗透保护剂甘氨酸甜菜碱的浓度增加。本报告证明了生长培养基的渗透压能够调节甘氨酸甜菜碱作为碳源、氮源或渗透保护剂的利用。同时比较了苜蓿根瘤菌和大肠杆菌中的渗透调节机制。