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原胶原模型的酶促羟基化作用。

The enzymic hydroxylation of protocollagen models.

作者信息

Kikuchi Y, Fujimoto D, Tamiya N

出版信息

Biochem J. 1969 Nov;115(3):569-74. doi: 10.1042/bj1150569.

Abstract
  1. Synthetic polymers of l-prolyl-l-prolylglycine of defined chain length, (Pro-Pro-Gly)(n), were found to be substrates for the enzyme protocollagen-proline hydroxylase, with optimum chain length n=5. Boiling the polymer (Pro-Pro-Gly)(15) increased its activity as a substrate but had no effect on (Pro-Pro-Gly)(5). 2. Protection of both or one of the N- and C-terminal groups made (Pro-Pro-Gly)(3) a better substrate, and collagenase digestion of hydroxylated tert.-pentyloxy-carbonyl-(Pro-Pro-Gly)(3) benzyl ester indicated that the central prolyl residues were the major points of hydroxylation. 3. The results suggest that the long-chain peptides are optimum substrates but that a triple-stranded structure is inhibitory for hydroxylation.
摘要
  1. 已发现具有特定链长的L-脯氨酰-L-脯氨酰甘氨酸的合成聚合物(Pro-Pro-Gly)(n)是原胶原-脯氨酸羟化酶的底物,最佳链长为n = 5。将聚合物(Pro-Pro-Gly)(15)煮沸可提高其作为底物的活性,但对(Pro-Pro-Gly)(5)没有影响。2. 对N端和C端基团中的一个或两个进行保护,使(Pro-Pro-Gly)(3)成为更好的底物,对羟基化的叔戊氧基羰基-(Pro-Pro-Gly)(3)苄酯进行胶原酶消化表明,中间的脯氨酰残基是主要的羟基化位点。3. 结果表明,长链肽是最佳底物,但三链结构对羟基化具有抑制作用。

相似文献

9
[Protocollagen proline hydroxylase].[原胶原蛋白脯氨酸羟化酶]
Tanpakushitsu Kakusan Koso. 1969 Feb;14(2):101-8.

本文引用的文献

1
Hydrolysis of synthetic peptides by collagenase.胶原酶对合成肽的水解作用。
Biochim Biophys Acta. 1960 Jan 29;37:567-9. doi: 10.1016/0006-3002(60)90531-x.
3
The structure of collagen and gelatin.胶原蛋白和明胶的结构。
Adv Protein Chem. 1961;16:1-138. doi: 10.1016/s0065-3233(08)60028-5.
9
Hydroxylation of proline in collagen model peptide.胶原蛋白模型肽中脯氨酸的羟基化作用。
Biochim Biophys Acta. 1969 Feb 18;177(1):154-6. doi: 10.1016/0304-4165(69)90077-4.

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