Piepersberg W, Böck A, Yaguchi M, Wittmann H G
Mol Gen Genet. 1975 Dec 30;143(1):43-52. doi: 10.1007/BF00269419.
The relative genetic position of the following four mutations of ribosomal protein S5 has been determined: spc-13, a mutation to spectinomycin resistance; stri N421 and strid1023, mutations suppressing dependence on streptomycin and sup0-1, a mutation suppressing partially the temperature-sensitive phenotype of an alanyl-tRNA synthetase mutation. The transduction experiments performed indicate that the spc-13 site is located in the S5 cistron proximal to the strA locus, that sup0-1 maps proximal to the aroE gene and that the striN421 and strid1023 loci are located between these two mutational sites. Proteinchemical analysis of the amino acid replacement in protein S5 of strain N421 (carrying the striN421 allele) has shown that an arginine residue is replaced by leucine which results in the appearance of a trypsin intensitive bond between the tryptic peptides T2 and T16. The same alteration has been previously found by Itoh and Wittmann (1973) in the S5 protein of strain d1023. Determination of the alteration of ribosomal protein S5 of strain 0-1 (sup0-1 allele) revealed that the C-terminal tryptic peptide is altered. It differs from that of the wild-type protein by the lack of five amino acids and the appearance of a C-terminal glycine residue instead of a lysine residue. This change can be explained by the deletion of eleven nucleotides in the S5 cistron of strain 0-1. The recent determination of the primary structure of ribosomal protein S5 (Wittmann-Liebold and Greuer, 1975) allows the ordering of the S5 alterations employed: The order is spc-13-strid1023 (striN421)-sup0-1 with the spc-13 amino acid replacement being located at the NH2-terminal portion of the S5 sequence and the alteration of strain 0-1 at the COOH-terminal end. The proteinchemical results are therefore in full agreement with the genetic data and unambiguously allow the conclusion that the S5 cistron is transcribed counterclock-wise on the Escherichia coli chromosome.
已确定核糖体蛋白S5的以下四种突变的相对遗传位置:spc - 13,一种对壮观霉素产生抗性的突变;stri N421和strid1023,抑制对链霉素依赖性的突变;以及sup0 - 1,一种部分抑制丙氨酰 - tRNA合成酶突变的温度敏感表型的突变。所进行的转导实验表明,spc - 13位点位于strA基因座近端的S5顺反子中,sup0 - 1定位于aroE基因近端,而striN421和strid1023位点位于这两个突变位点之间。对携带striN421等位基因的N421菌株的蛋白S5中的氨基酸置换进行的蛋白质化学分析表明,一个精氨酸残基被亮氨酸取代,这导致胰蛋白酶肽T2和T16之间出现一个对胰蛋白酶敏感的键。Itoh和Wittmann(1973年)先前在d1023菌株的S5蛋白中也发现了相同的改变。对0 - 1菌株(sup0 - 1等位基因)的核糖体蛋白S5的改变的测定表明,其C末端胰蛋白酶肽发生了改变。它与野生型蛋白的不同之处在于缺少五个氨基酸,并且出现了一个C末端甘氨酸残基而不是赖氨酸残基。这种变化可以通过0 - 1菌株的S5顺反子中11个核苷酸的缺失来解释。最近对核糖体蛋白S5一级结构的测定(Wittmann - Liebold和Greuer,1975年)使得所采用的S5改变能够排序:顺序为spc - 13 - strid1023(striN421) - sup0 - 1,其中spc - 13氨基酸置换位于S5序列的NH2末端部分,而0 - 1菌株的改变位于COOH末端。因此,蛋白质化学结果与遗传数据完全一致,并且明确地得出结论:S5顺反子在大肠杆菌染色体上以逆时针方向转录。