Bartsch M
J Biol Chem. 1985 Jan 10;260(1):237-41.
Immunological homology between chloroplast ribosomal proteins (r-proteins) from a higher plant (Spinacia) and bacterial r-proteins was examined using antibodies prepared against 35 purified Escherichia coli r-proteins. Cross-reactions were determined on cellulose acetate gels and on nitrocellulose paper, after electrophoretic transfer of r-proteins from one- and two dimensional polyacrylamide gels, using peroxidase and fluorescein-conjugated second antibodies for detection (immunoblotting). The specificity of positive cross-reactions was confirmed by absorption experiments using purified E. coli r-proteins. Antisera against five proteins of the small subunit and six proteins of the large subunit of E. coli ribosome (i.e. anti-S7, -S9, -S11, -S12, and -S19; anti-L1, -L2, -L3, -L6, -L13, and -L17) gave cross-reactions. As an inference from this work, and a recent study on the synthesis of certain chloroplast r-proteins in isolated chloroplasts (Eneas-Filho, J., Hartley, M. R., and Mache, R. (1981) Mol. Gen. Genet. 184, 484-488), we suggest that chloroplast r-proteins S7 and L2 are encoded in the organelle DNA.
利用针对35种纯化的大肠杆菌核糖体蛋白(r蛋白)制备的抗体,检测了高等植物(菠菜)叶绿体核糖体蛋白与细菌r蛋白之间的免疫同源性。在将r蛋白从一维和二维聚丙烯酰胺凝胶电泳转移至醋酸纤维素凝胶和硝酸纤维素纸上后,使用过氧化物酶和荧光素偶联的二抗进行检测(免疫印迹),以确定交叉反应。通过使用纯化的大肠杆菌r蛋白进行吸收实验,证实了阳性交叉反应的特异性。针对大肠杆菌核糖体小亚基的5种蛋白和大亚基的6种蛋白的抗血清(即抗-S7、-S9、-S11、-S12和-S19;抗-L1、-L2、-L3、-L6、-L13和-L17)产生了交叉反应。基于这项工作以及最近关于在分离的叶绿体中某些叶绿体r蛋白合成的研究(Eneas-Filho, J., Hartley, M. R., and Mache, R. (1981) Mol. Gen. Genet. 184, 484 - 488),我们认为叶绿体r蛋白S7和L2由细胞器DNA编码。