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蓖麻乙醛酸循环体异柠檬酸裂解酶靶向烟草叶片过氧化物酶体。

Targeting of castor bean glyoxysomal isocitrate lyase to tobacco leaf peroxisomes.

作者信息

Onyeocha I, Behari R, Hill D, Baker A

机构信息

Department of Biochemistry, University of Cambridge, UK.

出版信息

Plant Mol Biol. 1993 Jun;22(3):385-96. doi: 10.1007/BF00015970.

Abstract

The cDNA encoding castor bean endosperm isocitrate lyase (ICL) was expressed under the control of the promoter of the small subunit of pea ribulose bisphosphate carboxylase in transformed tobacco. ICL protein was detected using anti-ICL antibodies on immunoblots of total leaf protein extracts. Nycodenz density gradient separation of the extracts from the transgenic tobacco leaves showed ICL co-fractionated with hydroxypyruvate reductase, a peroxisomal matrix marker protein, and away from lactate dehydrogenase, a cytosolic marker protein. Immunoelectron microscopy of ultrathin leaf sections demonstrated the location of ICL within the matrix of the leaf peroxisomes of the transgenic plants. In vitro transcribed and translated ICL was also imported into leaf peroxisomes isolated from germinating sunflower seeds. The in vivo and in vitro import of this protein into leaf peroxisomes provides strong support for the notion that the import machinery of glyoxysomes and peroxisomes is very similar.

摘要

编码蓖麻籽胚乳异柠檬酸裂解酶(ICL)的cDNA在豌豆核酮糖二磷酸羧化酶小亚基启动子的控制下,在转基因烟草中表达。使用抗ICL抗体在总叶蛋白提取物的免疫印迹上检测到ICL蛋白。对转基因烟草叶片提取物进行的Nycodenz密度梯度分离显示,ICL与过氧化物酶体基质标记蛋白羟基丙酮酸还原酶共分离,而与胞质标记蛋白乳酸脱氢酶分离。对超薄叶切片进行免疫电子显微镜观察,证实了转基因植物叶片过氧化物酶体基质中ICL的定位。体外转录和翻译的ICL也被导入从发芽向日葵种子中分离出的叶过氧化物酶体。该蛋白在体内和体外导入叶过氧化物酶体,为乙醛酸循环体和过氧化物酶体的导入机制非常相似这一观点提供了有力支持。

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