Salomon M, Fischer K, Flügge U I, Soll J
Botanisches Institut, Universität Munich, Federal Republic of Germany.
Proc Natl Acad Sci U S A. 1990 Aug;87(15):5778-82. doi: 10.1073/pnas.87.15.5778.
A chloroplast outer envelope membrane protein was cloned and sequenced and from the sequence it was possible to deduce a polypeptide of 6.7 kDa. It has only one membrane-spanning region; the C terminus extends into the cytosol, whereas the N terminus is exposed to the space between the two envelope membranes. The protein was synthesized in an in vitro transcription-translation system to study its routing into isolated chloroplasts. The import studies revealed that the 6.7-kDa protein followed a different and heretofore undescribed translocation pathway in the respect that (i) it does not have a cleavable transit sequence, (ii) it does not require ATP hydrolysis for import, and (iii) protease-sensitive components that are responsible for recognition of precursor proteins destined for the inside of the chloroplasts are not involved in routing the 6.7-kDa polypeptide to the outer chloroplast envelope.
克隆并测序了一种叶绿体外被膜蛋白,从该序列可以推断出一个6.7 kDa的多肽。它只有一个跨膜区域;C末端延伸到细胞质中,而N末端暴露在两层被膜之间的空间中。在体外转录-翻译系统中合成该蛋白,以研究其进入分离叶绿体的途径。导入研究表明,6.7 kDa的蛋白遵循一种不同的、迄今为止未描述的转运途径,即:(i)它没有可裂解的转运序列,(ii)它的导入不需要ATP水解,(iii)负责识别进入叶绿体内部的前体蛋白的蛋白酶敏感成分不参与将6.7 kDa多肽转运到叶绿体外被膜。