Liu J, Burns D M, Beacham I R
J Bacteriol. 1986 Mar;165(3):1002-10. doi: 10.1128/jb.165.3.1002-1010.1986.
The cpdB gene encodes a periplasmic 2',3'-cyclic phosphodiesterase (3'-nucleotidase). This enzyme has been purified previously and the gene is located at 96 min on the Escherichia coli chromosome. In this study the cpdB gene was cloned from ClaI-cleaved DNA, and the gene product was identified. DNA blotting experiments showed that the recombinant plasmid contains a deletion with respect to the expected genomic fragment of approximately 4 kilobases, which extends into the vector. Furthermore, the gene was absent from three other recombinant libraries. Together, these findings suggest the presence in the genome of an adjacent gene whose product is lethal when it is present on a multicopy plasmid. The nucleotide sequence of the cpdB gene was also determined. The 5' and 3' untranslated sequences contain characteristic sequences that are involved in the initiation and termination of transcription, including two possible promoters, one of which may contain two overlapping -10 sequences. A strong Shine-Dalgarno sequence is followed by an open reading frame which corresponds to a protein having a molecular weight of 70,954. The first 19 amino acid residues have the characteristics of a signal peptide. The 3' untranslated sequence contains two putative rho-independent transcription terminators having low thermodynamic stability.
cpdB基因编码一种周质2',3'-环磷酸二酯酶(3'-核苷酸酶)。该酶先前已被纯化,其基因位于大肠杆菌染色体的96分钟处。在本研究中,cpdB基因是从经ClaI酶切的DNA中克隆出来的,并对基因产物进行了鉴定。DNA印迹实验表明,重组质粒相对于预期的约4千碱基的基因组片段存在缺失,该缺失延伸到载体中。此外,另外三个重组文库中也没有该基因。这些发现共同表明,基因组中存在一个相邻基因,当其存在于多拷贝质粒上时,其产物具有致死性。还测定了cpdB基因的核苷酸序列。5'和3'非翻译序列包含参与转录起始和终止的特征性序列,包括两个可能的启动子,其中一个可能包含两个重叠的-10序列。一个强的Shine-Dalgarno序列后面跟着一个开放阅读框,该阅读框对应于一个分子量为70,954的蛋白质。前19个氨基酸残基具有信号肽的特征。3'非翻译序列包含两个推定的不依赖于rho的转录终止子,其热力学稳定性较低。