Jensen K F, Larsen J N, Schack L, Sivertsen A
Eur J Biochem. 1984 Apr 16;140(2):343-52. doi: 10.1111/j.1432-1033.1984.tb08107.x.
The Escherichia coli pyrC, pyrD and pyrF genes were cloned on multicopy plasmids derived from pBR322 and analysed by means of restriction endonucleases. It was found that the pyrC gene is destroyed by cutting with the restriction endonuclease BamHI, that the entire pyrD gene can be isolated on a 1300-base pairs DNA fragment generated by EcoRI cleavage and that cutting with EcoRI removes the promotor and probably also the translational start site from the pyrF gene. More details on the restriction maps are presented. Further, it was found that the presence of a pyr gene in multiple copies on a plasmid does not significantly interfere with the activity of the chromosomal pyr genes. Using the 'minicell' technique, the polypeptides encoded by the three cloned pyr genes were identified. The relative molecular masses for the pyrC-encoded and pyrD-encoded polypeptides are 38 000-40 000 and 36 000-38 000, respectively. Thus in their native form, dihydroorotase and dihydroorotate oxidase appear to be dimeric proteins. The 'minicell' experiments positively identified a protein chain of Mr 23 000-24 000 as being a subunit of OMP decarboxylase encoded by pyrF. Moreover, the coding frame for this polypeptide seems to be expressed as the first gene in the operon with the coding frame for another protein chain of Mr 13 000-14 000. Since, however, the native OMP decarboxylase during sedimentation and gel filtration behaves as a protein of Mr 45 000 +/- 4000, this latter polypeptide (Mr 13 000-14 000) is hardly a component of the enzyme. Pyr-lac+ operon fusions were constructed by the Mu d1 procedure. By integrating an F'lac episome into the lac part of the fusions and determining the direction of chromosomal transfer from the resultant Hfr strains, the direction of pyrC transcription was found to be counter-clockwise, while pyrD and pyrF were found to be transcribed in a clockwise direction.
将大肠杆菌的pyrC、pyrD和pyrF基因克隆到源自pBR322的多拷贝质粒上,并用限制性内切酶进行分析。发现用限制性内切酶BamHI切割会破坏pyrC基因,用EcoRI切割可在产生的1300个碱基对的DNA片段上分离出完整的pyrD基因,用EcoRI切割会从pyrF基因上去除启动子,可能还会去除翻译起始位点。文中给出了更多关于限制性图谱的细节。此外,还发现质粒上多拷贝存在的pyr基因不会显著干扰染色体上pyr基因的活性。利用“微小细胞”技术,鉴定了由三个克隆的pyr基因编码的多肽。pyrC编码的多肽和pyrD编码的多肽的相对分子质量分别为38000 - 40000和36000 - 38000。因此,天然形式的二氢乳清酸酶和二氢乳清酸氧化酶似乎是二聚体蛋白。“微小细胞”实验明确鉴定出一条相对分子质量为23000 - 24000的蛋白质链是由pyrF编码的OMP脱羧酶的一个亚基。此外,该多肽的编码框似乎与另一条相对分子质量为13000 - 14000的蛋白质链的编码框一起作为操纵子中的第一个基因表达。然而,由于天然的OMP脱羧酶在沉降和凝胶过滤过程中的行为表现为相对分子质量为45000±4000的蛋白质,所以后一种多肽(相对分子质量为13000 - 14000)几乎不是该酶的组成成分。通过Mu d1程序构建了Pyr - lac +操纵子融合体。通过将F'lac附加体整合到融合体的lac部分,并确定所得Hfr菌株中染色体转移的方向,发现pyrC的转录方向是逆时针的,而pyrD和pyrF的转录方向是顺时针的。