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用多聚磷酸葡萄糖激酶测定多聚磷酸盐的大小。

Determination of the size of polyphosphates with polyphosphate glucokinase.

作者信息

Pepin C A, Wood H G, Robinson N A

出版信息

Biochem Int. 1986 Jan;12(1):111-23.

PMID:3004497
Abstract

A procedure for determining the size of inorganic polyphosphates of chain lengths up to about 750 is described. It involves reducing the size with polyphosphate glucokinase to a chain length that can be accurately determined by polyacrylamide gel electrophoresis. This measurement along with determination of the glucose-6-P formed and the total phosphate of the original polyphosphate permits calculation of the chain length. The accuracy of this method has been demonstrated by comparison with other reliable procedures. Thus far, it is the only method available for sizing long chain polyphosphates with nmol quantities.

摘要

本文描述了一种用于测定链长高达约750的无机多磷酸盐大小的方法。该方法包括用多磷酸盐葡萄糖激酶将其大小减小至可通过聚丙烯酰胺凝胶电泳准确测定的链长。这种测量以及对形成的6-磷酸葡萄糖和原始多磷酸盐总磷酸盐的测定允许计算链长。通过与其他可靠方法比较证明了该方法的准确性。到目前为止,它是唯一可用于对纳摩尔量的长链多磷酸盐进行大小测定的方法。

相似文献

1
Determination of the size of polyphosphates with polyphosphate glucokinase.用多聚磷酸葡萄糖激酶测定多聚磷酸盐的大小。
Biochem Int. 1986 Jan;12(1):111-23.
2
Preparation of standards and determination of sizes of long-chain polyphosphates by gel electrophoresis.长链多聚磷酸盐标准品的制备及通过凝胶电泳测定其大小
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Biochem Int. 1984 Jun;8(6):757-69.
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Polyphosphate kinase from Propionibacterium shermanii. Demonstration that polyphosphates are primers and determination of the size of the synthesized polyphosphate.来自谢氏丙酸杆菌的多聚磷酸激酶。证明多聚磷酸盐是引物并测定合成的多聚磷酸的大小。
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Polyphosphate glucokinase from Propionibacterium shermanii. Kinetics and demonstration that the mechanism involves both processive and nonprocessive type reactions.来自谢氏丙酸杆菌的多聚磷酸葡萄糖激酶。动力学及机制涉及连续型和非连续型反应的证明。
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Determination of endopolyphosphatase using polyphosphate glucokinase.使用多聚磷酸葡萄糖激酶测定胞内多聚磷酸酶
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引用本文的文献

1
Isolation of intact chains of polyphosphate from "Propionibacterium shermanii" grown on glucose or lactate.从在葡萄糖或乳酸上生长的“谢氏丙酸杆菌”中分离聚磷酸盐的完整链。
J Bacteriol. 1986 Dec;168(3):1212-9. doi: 10.1128/jb.168.3.1212-1219.1986.