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一种涉及集胞藻PCC 6803中分支酸合酶(芳香族生物合成途径)基因和核糖体GTPase中心蛋白(L11、L1、L10、L12:rplKAJL)的新型操纵子组织。

A novel operon organization involving the genes for chorismate synthase (aromatic biosynthesis pathway) and ribosomal GTPase center proteins (L11, L1, L10, L12: rplKAJL) in cyanobacterium Synechocystis PCC 6803.

作者信息

Schmidt J, Bubunenko M, Subramanian A R

机构信息

Max-Planck-Institut für Molekulare Genetik, Berlin-Dahlem, Germany.

出版信息

J Biol Chem. 1993 Dec 25;268(36):27447-57.

PMID:7505271
Abstract

Many of the ribosomal protein (RP) genes in both bacterial and chloroplast genomes occur, for reasons not yet understood, in operons that include nonribosomal genes. Here we report such an operon organization in a cyanobacterium (Synechocystis PCC6803) involving the genes for four RPs that are important in the GTPase function of the ribosome and the aroC gene encoding chorismate synthase, a key enzyme in the shikimate pathway for biosynthesis of aromatic amino acids and cell wall components. The Synechocystis aroC encodes a 362-amino-acid residue protein which is 52, 60, and 68% identical to two eubacterial (both 52%), yeast, and a higher plant (Corydalis) chorismate synthase, respectively. The gene was overexpressed in Escherichia coli, and the gene product was shown to cross-react with antibodies to Corydalis chorismate synthase; it also complemented an aroC-lacking E. coli strain. The Synechocystis rpl1 and rpl11 genes encode polypeptides of 237 and 141 amino acid residues, respectively, also with high sequence identities to the corresponding RP sequences from other eubacteria and higher plant chloroplasts. The gene order is shown to be: rpl11-86bp spacer-rpl1-460bp spacer-rpl10-87-bp spacer-rpl12-206bp spacer-aroC. Southern and Northern blot analyses of Synechocystis DNA and RNA, respectively, revealed a single cluster of these genes per genome which is transcribed from a common promoter to an unusually long, approximately 9500-nucleotide transcript. Several constructs of the cyanobacterial aroC and rpl12 genes were made and expressed in E. coli to examine the mechanisms for their very differential expression from a polycistronic mRNA (e.g. four copies L12/ribosome; chorismate synthase, a non-abundant protein). These results present the first biochemical/molecular genetic evidence of shikimate pathway in the cyanobacterial group.

摘要

细菌和叶绿体基因组中的许多核糖体蛋白(RP)基因,由于尚未明确的原因,存在于包含非核糖体基因的操纵子中。在此,我们报道了一种蓝细菌(集胞藻PCC6803)中的操纵子组织,它涉及四个对核糖体GTPase功能很重要的RP基因以及编码分支酸合酶的aroC基因,分支酸合酶是芳香族氨基酸和细胞壁成分生物合成的莽草酸途径中的关键酶。集胞藻aroC编码一个362个氨基酸残基的蛋白质,它与两种真细菌(均为52%)、酵母以及一种高等植物(紫堇属)的分支酸合酶的同源性分别为52%、60%和68%。该基因在大肠杆菌中过表达,并且基因产物显示与抗紫堇属分支酸合酶的抗体发生交叉反应;它还能互补缺乏aroC的大肠杆菌菌株。集胞藻rpl1和rpl11基因分别编码237和141个氨基酸残基的多肽,与来自其他真细菌和高等植物叶绿体的相应RP序列也具有高度的序列同源性。基因顺序显示为:rpl11 - 86bp间隔区 - rpl1 - 460bp间隔区 - rpl10 - 87bp间隔区 - rpl12 - 206bp间隔区 - aroC。分别对集胞藻DNA和RNA进行的Southern和Northern印迹分析表明,每个基因组中这些基因形成一个单一的簇,从一个共同的启动子转录成一个异常长的、约9500个核苷酸的转录本。构建了几种蓝细菌aroC和rpl12基因的构建体并在大肠杆菌中表达,以研究它们在多顺反子mRNA中差异极大的表达机制(例如,四个拷贝的L12/核糖体;分支酸合酶,一种非丰富蛋白)。这些结果提供了蓝细菌群体中莽草酸途径的首个生化/分子遗传学证据。

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