Stoker N G, Pratt J M, Spratt B G
J Bacteriol. 1983 Aug;155(2):854-9. doi: 10.1128/jb.155.2.854-859.1983.
Plasmids that carry the Escherichia coli cell shape gene rodA directed the synthesis of a cytoplasmic membrane protein (Mr, 31,000 [31K protein] ) in minicells, maxicells, and an in vitro-coupled transcription-translation system. The 31K protein was identified as the rodA gene product, because it was not synthesized from the vector plasmids or from a plasmid in which the rodA gene was inactivated by insertion of Tn1000. Furthermore, a purified 1.6-kilobase KpnI-BamHI DNA fragment that contained the intact rodA gene directed the synthesis of only the 31K protein in an in vitro system. The apparent molecular weight of the protein was identical whether synthesized in vivo or in vitro, indicating that the rodA gene product is not made as a preprotein. The direction of transcription of rodA was from the KpnI site towards the BamHI site. The 31K protein was unusual in that it could only be detected when cell membranes were solubilized at low temperature (e.g., 37 degrees C) before sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Apparently the rodA gene product aggregates after being boiled in sodium dodecyl sulfate and fails to enter a polyacrylamide gel.
携带大肠杆菌细胞形状基因rodA的质粒,在小细胞、大细胞以及体外偶联转录-翻译系统中,指导合成一种细胞质膜蛋白(分子量为31,000 [31K蛋白])。31K蛋白被鉴定为rodA基因产物,因为它不是由载体质粒或rodA基因因插入Tn1000而失活的质粒合成的。此外,一个纯化的1.6千碱基的KpnI - BamHI DNA片段,包含完整的rodA基因,在体外系统中仅指导31K蛋白的合成。无论在体内还是体外合成,该蛋白的表观分子量都相同,这表明rodA基因产物不是以前体蛋白的形式合成的。rodA的转录方向是从KpnI位点朝向BamHI位点。31K蛋白不同寻常之处在于,只有在低温(如37℃)下将细胞膜溶解后进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳时才能检测到它。显然,rodA基因产物在十二烷基硫酸钠中煮沸后会聚集,无法进入聚丙烯酰胺凝胶。