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产甲酸草酸杆菌草酸辅酶A脱羧酶基因的克隆与表达:基因治疗控制草酸钙肾结石形成的前景

Cloning and expression of the oxalyl-CoA decarboxylase gene from the bacterium, Oxalobacter formigenes: prospects for gene therapy to control Ca-oxalate kidney stone formation.

作者信息

Lung H Y, Cornelius J G, Peck A B

机构信息

Department of Pathology and Laboratory Medicine, University of Florida College of Medicine, Gainesville 32610.

出版信息

Am J Kidney Dis. 1991 Apr;17(4):381-5. doi: 10.1016/s0272-6386(12)80627-5.

Abstract

Evidence suggests that the formation of calcium-oxalate stones in the urine is dependent on the saturation levels of both calcium and oxalate; thus, management of one or both of these ions in individuals susceptible to urolithiasis appears important. Since there are no known naturally occurring enzymes in vertebrates capable of degrading oxalate, we have initiated a study to insert a plant-derived oxalate degrading enzyme gene into human cells as a means of lowering plasma and urinary oxalate concentrations. We present here the cloning of the oxalyl-CoA decarboxylase gene from the bacterium Oxalobacter formigenes and its subsequent expression in a foreign environment. These results provide the basis for eventual transfer of an oxalate decarboxylase gene into mammalian cells.

摘要

有证据表明,尿液中草酸钙结石的形成取决于钙和草酸的饱和水平;因此,对于易患尿路结石的个体,对其中一种或两种离子进行管理显得很重要。由于在脊椎动物中尚未发现能降解草酸的天然存在的酶,我们已启动一项研究,将一种植物源草酸降解酶基因导入人体细胞,以此降低血浆和尿液中的草酸浓度。我们在此展示了从产甲酸草酸杆菌中克隆草酰辅酶A脱羧酶基因及其随后在异源环境中的表达。这些结果为最终将草酸脱羧酶基因转入哺乳动物细胞奠定了基础。

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