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完整马铃薯造粉体中磷酸化淀粉的体外生物合成。

In vitro biosynthesis of phosphorylated starch in intact potato amyloplasts.

作者信息

Wischmann B

机构信息

Plant Biochemistry Laboratory, Department of Plant Biology, The Royal Veterinary and Agricultural University, 40 Thorvaldsensvej, DK-1871 Frederiksberg C, Copenhagen, Denmark.

出版信息

Plant Physiol. 1999 Feb;119(2):455-62. doi: 10.1104/pp.119.2.455.

Abstract

Intact amyloplasts from potato (Solanum tuberosum L.) were used to study starch biosynthesis and phosphorylation. Assessed by the degree of intactness and by the level of cytosolic and vacuolar contamination, the best preparations were selected by searching for amyloplasts containing small starch grains. The isolated, small amyloplasts were 80% intact and were free from cytosolic and vacuolar contamination. Biosynthetic studies of the amyloplasts showed that [1-14C]glucose-6-phosphate (Glc-6-P) was an efficient precursor for starch synthesis in a manner highly dependent on amyloplast integrity. Starch biosynthesis from [1-14C]Glc-1-P in small, intact amyloplasts was 5-fold lower and largely independent of amyloplast intactness. When [33P]Glc-6-P was administered to the amyloplasts, radiophosphorylated starch was produced. Isoamylase treatment of the starch followed by high-performance anion-exchange chromatography with pulsed amperometric detection revealed the separated phosphorylated alpha-glucans. Acid hydrolysis of the phosphorylated alpha-glucans and high-performance anion-exchange chromatography analyses showed that the incorporated phosphate was preferentially positioned at C-6 of the Glc moiety. The incorporation of radiolabel from Glc-1-P into starch in preparations of amyloplasts containing large grains was independent of intactness and most likely catalyzed by starch phosphorylase bound to naked starch grains.

摘要

利用来自马铃薯(Solanum tuberosum L.)的完整造粉体研究淀粉的生物合成和磷酸化作用。通过完整性程度以及胞质和液泡污染水平进行评估,通过寻找含有小淀粉粒的造粉体来选择最佳制剂。分离得到的小造粉体完整性达80%,且无胞质和液泡污染。对造粉体的生物合成研究表明,[1-14C]葡萄糖-6-磷酸(Glc-6-P)是淀粉合成的有效前体,其方式高度依赖于造粉体的完整性。在小的完整造粉体中,由[1-14C]Glc-1-P合成淀粉的效率低5倍,且在很大程度上与造粉体的完整性无关。当向造粉体中加入[33P]Glc-6-P时,会产生放射性磷酸化淀粉。对淀粉进行异淀粉酶处理,然后用脉冲安培检测的高效阴离子交换色谱法可分离出磷酸化的α-葡聚糖。对磷酸化的α-葡聚糖进行酸水解和高效阴离子交换色谱分析表明,掺入的磷酸盐优先位于Glc部分的C-6位。在含有大颗粒的造粉体制剂中,Glc-1-P的放射性标记掺入淀粉的过程与完整性无关,很可能是由与裸露淀粉粒结合的淀粉磷酸化酶催化的。

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