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环状β-1,2-葡聚糖生物合成中的一种中间体。

An intermediate in cyclic beta 1-2 glucan biosynthesis.

作者信息

Zorreguieta A, Ugalde R A, Leloir L F

出版信息

Biochem Biophys Res Commun. 1985 Jan 16;126(1):352-7. doi: 10.1016/0006-291x(85)90613-8.

Abstract

Incubation of UDP-[14C]Glc with the inner membranes of Agrobacterium tumefaciens leads to the formation of cyclic beta 1-2 glucan and trichloroacetic acid-insoluble compounds. The proteolysis products of the latter show a positive charge in acid and a negative charge in alkaline buffers. The cyclic beta 1-2 glucan and the trichloroacetic acid insoluble compounds yield the same products on partial acid hydrolysis. Addition of excess non-radioactive UDP-Glc to the reaction mixture nearly stops the formation of radioactive beta 1-2 glucan and leads to a rapid fall of radioactivity in the trichloroacetic acid precipitate. Alkaline treatment of the insoluble compounds under conditions of beta-elimination leads to the partial release of free saccharides (about 30%). It is concluded that beta 1-2 glucan chains are built up joined to a protein and then released as free cyclic beta 1-2 glucan.

摘要

用UDP-[14C]葡萄糖与根癌土壤杆菌的内膜一起温育会导致环状β-1,2-葡聚糖和三氯乙酸不溶性化合物的形成。后者的蛋白水解产物在酸性缓冲液中带正电荷,在碱性缓冲液中带负电荷。环状β-1,2-葡聚糖和三氯乙酸不溶性化合物在部分酸水解时产生相同的产物。向反应混合物中加入过量的非放射性UDP-葡萄糖几乎会停止放射性β-1,2-葡聚糖的形成,并导致三氯乙酸沉淀物中的放射性迅速下降。在β-消除条件下对不溶性化合物进行碱性处理会导致部分游离糖类的释放(约30%)。可以得出结论,β-1,2-葡聚糖链先与一种蛋白质连接形成,然后以游离环状β-1,2-葡聚糖的形式释放出来。

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