Plant Environmental Biology Group, Research School of Biological Sciences, Australian National University, P.O. Box 475, Canberra City, A.C.T. 2601. Australia.
Plant Physiol. 1988 Dec;88(4):1048-54. doi: 10.1104/pp.88.4.1048.
The transport of l-[(14)C]glutamine in oat (Avena sativa L.) and spinach (Spinacia oleracea L.) chloroplasts was studied by a conventional single-layer and a newly developed stable double-layer silicone oil filtering system. [(14)C]Glutamine was actively transported into oat chloroplasts against a concentration gradient. Metabolite uptake was greatly affected by the endogenous dicarboxylate pools, which could be easily changed by preloading the chloroplast with specific exogenous substrate. Glutamine uptake was decreased by 44 to 75% in oat chloroplasts preloaded with malate, 2-oxoglutarate (2-OG), and aspartate, but increased by 52% in chloroplasts preloaded with l-glutamate. On the other hand, the uptake of the other four dicarboxylates was decreased by 47 to 79% in chloroplasts preloaded with glutamine. In glutamine-preloaded chloroplasts the uptake of glutamine was inhibited only by l-glutamate. The observed inhibition by l-glutamate was competitive with an apparent K(i) value of 32.1 millimolar in oat and 6.7 millimolar in spinach chloroplasts. This study indicates that there are two components involved in glutamine transport in chloroplasts. The major component was mediated via a specific glutamine translocator. It was specific for glutamine and did not transport other dicarboxylates except l-glutamate. A K(0.5) value of 1.25 millimolar and V(max) of 45.5 micromoles per milligram of chlorophyll per hour were determined for the glutamine translocator in oat chloroplasts. The respective values were 1.0 millimolar and 16.7 micromoles per milligram of chlorophyll per hour in spinach chloroplasts. A three translocator model, involving the glutamine, dicarboxylate, and 2-OG translocators, is proposed for the reassimilation of photorespiratory NH(3) in chloroplasts of C(3) species. In this three-translocator model the additional transport of glutamine into the chloroplast is coupled to the export of glutamate via the glutamine translocator. This is an extension of the two-translocator model, involving the dicarboxylate and 2-OG translocators, proposed for spinach chloroplasts, (KC Woo, UI Flügge, HW Heldt 1987 Plant Physiol 84: 624-632).
我们使用传统的单层和新开发的稳定双层硅油过滤系统研究了燕麦(Avena sativa L.)和菠菜(Spinacia oleracea L.)叶绿体中 l-[(14)C]谷氨酰胺的转运。[(14)C]谷氨酰胺能够逆浓度梯度主动转运进入燕麦叶绿体。代谢物摄取受内源性二羧酸库的影响很大,通过用特定的外源性底物预载叶绿体,可以很容易地改变二羧酸库。在预先用苹果酸、2-氧戊二酸(2-OG)和天冬氨酸装载的燕麦叶绿体中,谷氨酰胺摄取减少了 44%至 75%,但在预先用 l-谷氨酸装载的叶绿体中增加了 52%。另一方面,在预先用谷氨酰胺装载的叶绿体中,其他四种二羧酸的摄取减少了 47%至 79%。在预先用谷氨酰胺装载的叶绿体中,只有 l-谷氨酸能抑制谷氨酰胺的摄取。在燕麦和菠菜叶绿体中,l-谷氨酸的抑制作用是竞争性的,表观 K(i)值分别为 32.1 毫摩尔和 6.7 毫摩尔。这项研究表明,叶绿体中谷氨酰胺的转运涉及两个组成部分。主要成分是通过一种特定的谷氨酰胺转运蛋白介导的。它对谷氨酰胺具有特异性,除 l-谷氨酸外,不转运其他二羧酸。在燕麦叶绿体中,谷氨酰胺转运蛋白的 K(0.5)值为 1.25 毫摩尔,V(max)值为每毫克叶绿素每小时 45.5 微摩尔。在菠菜叶绿体中,相应的值分别为 1.0 毫摩尔和每毫克叶绿素每小时 16.7 微摩尔。提出了一个涉及谷氨酰胺、二羧酸和 2-OG 转运蛋白的三转运蛋白模型,用于 C(3)物种叶绿体中光呼吸 NH(3)的再同化。在这个三转运蛋白模型中,谷氨酰胺通过谷氨酰胺转运蛋白进入叶绿体的额外转运与谷氨酸通过谷氨酰胺转运蛋白的输出偶联。这是一个涉及二羧酸和 2-OG 转运蛋白的二转运蛋白模型的扩展,该模型用于菠菜叶绿体(KC Woo、UI Flügge、HW Heldt 1987 年《植物生理学》84:624-632)。