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克隆出两个推测的蓝氏贾第鞭毛虫6-磷酸葡糖胺异构酶基因,其中只有一个在包囊形成过程中被转录激活。

Cloning of two putative Giardia lamblia glucosamine 6-phosphate isomerase genes only one of which is transcriptionally activated during encystment.

作者信息

Van Keulen H, Steimle P A, Bulik D A, Borowiak R K, Jarroll E L

机构信息

Department of Biological, Geological and Environmental Sciences, Cleveland State University, Ohio 44115, USA.

出版信息

J Eukaryot Microbiol. 1998 Nov-Dec;45(6):637-42. doi: 10.1111/j.1550-7408.1998.tb04560.x.

Abstract

The biosynthesis of the carbohydrate component of the cyst wall of the protozoan parasite Giardia lamblia, a polymer of N-acetylgalactosamine (GalNac), is by a pathway that is initiated with the conversion of fructose 6-phosphate to glucosamine 6-phosphate by an aminating isomerase, glucose 6-phosphate isomerase. This enzyme appears only after Giardia trophozoites are induced to start the production of cyst wall components after bile is added. To investigate whether induction of glucosamine 6-phosphate isomerase is by protein modification or by transcription activation, its gene was cloned and sequenced. Two genes, gpi1 and gpi2, encoding putative glucosamine 6-phosphate isomerases were identified but one, gpi1 was expressed. The transcript for gpi1 appeared not earlier than 6 h after cells were induced with bile salts. These results show that the first enzyme in the pathway leading to GalNac synthesis in encysting Giardia cyst wall biosynthesis is under transcriptional control.

摘要

原生动物寄生虫蓝氏贾第鞭毛虫囊壁碳水化合物成分是N - 乙酰半乳糖胺(GalNac)的聚合物,其生物合成途径始于氨基化异构酶葡萄糖6 - 磷酸异构酶将6 - 磷酸果糖转化为6 - 磷酸葡糖胺。该酶仅在添加胆汁后,贾第虫滋养体被诱导开始产生囊壁成分时才出现。为了研究6 - 磷酸葡糖胺异构酶的诱导是通过蛋白质修饰还是转录激活,对其基因进行了克隆和测序。鉴定出两个编码推定的6 - 磷酸葡糖胺异构酶的基因,gpi1和gpi2,但只有gpi1表达。在用胆盐诱导细胞后,gpi1的转录本最早不早于6小时出现。这些结果表明,在包囊的贾第虫囊壁生物合成中,导致GalNac合成途径中的第一种酶受转录控制。

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