McAllister C F, Lepo J E
J Bacteriol. 1983 Mar;153(3):1155-62. doi: 10.1128/jb.153.3.1155-1162.1983.
We have demonstrated that the transport of succinate into the cells of Rhizobium japonicum strains USDA 110 and USDA 217 is severely inhibited by cyanide, azide, and 2,4-dinitrophenol, but not by arsenate. These results suggest an active mechanism of transport that is dependent on an energized membrane, but does not directly utilize ATP. The apparent Km for succinate was 3.8 microM for strain USDA 110 and 1.8 microM for strain USDA 217; maximal transport velocities were 1.5 and 3.3 nmol of succinate per min per mg of protein, respectively. The expression of the succinate uptake activity was inducible rather than constitutive, with succinate and structurally related compounds being the most effective inducers. The mechanism showed some specificity for succinate and similar organic acids; fumarate and L-malate were classical competitive inhibitors of the system. In general, the best competing compounds were also the best carbon substrates for induction of succinate uptake activity. EDTA inhibited the transport of succinate, implying a role for divalent cations in the system. When various divalent cations were used to reconstitute EDTA-inhibited activity, Ca2+ was most effective, followed by Mg2+, which restored activity at about half the efficiency of Ca2+. Growth media that were supplemented with increased Ca2+ concentration supported more rapid growth with succinate as the carbon substrate, and cells from such media showed higher specific activities of succinate transport.
我们已经证明,琥珀酸转运到日本根瘤菌菌株USDA 110和USDA 217细胞中的过程受到氰化物、叠氮化物和2,4 -二硝基苯酚的严重抑制,但不受砷酸盐抑制。这些结果表明存在一种主动转运机制,该机制依赖于有能量的膜,但不直接利用ATP。菌株USDA 110对琥珀酸的表观Km为3.8 microM,菌株USDA 217为1.8 microM;最大转运速度分别为每分钟每毫克蛋白质1.5和3.3纳摩尔琥珀酸。琥珀酸摄取活性的表达是可诱导的而非组成型的,琥珀酸和结构相关化合物是最有效的诱导剂。该机制对琥珀酸和类似有机酸表现出一定的特异性;富马酸和L -苹果酸是该系统的经典竞争性抑制剂。一般来说,最佳竞争化合物也是诱导琥珀酸摄取活性的最佳碳源。EDTA抑制琥珀酸的转运,这意味着二价阳离子在该系统中起作用。当用各种二价阳离子来恢复EDTA抑制的活性时,Ca2+最有效,其次是Mg2+,其恢复活性的效率约为Ca2+的一半。补充了较高Ca2+浓度的生长培养基以琥珀酸作为碳源时支持更快的生长,并且来自这种培养基的细胞显示出更高的琥珀酸转运比活性。