Icho T, Sparrow C P, Raetz C R
J Biol Chem. 1985 Oct 5;260(22):12078-83.
The cds gene of Escherichia coli codes for the enzyme CDP-diglyceride synthetase. We now report the construction of plasmids which carry cds. Using these plasmids, we have sequenced 1274 base pairs of DNA, including a 750-base pair open reading frame which is the coding region of the cds gene. This DNA sequence allows the deduction of the primary peptide sequence for CDP-diglyceride synthetase. The protein is very hydrophobic, and, assuming no processing or modification, has a molecular weight of 27,570. Furthermore, there is a second open reading frame immediately after cds, implying that cds may be part of an operon. We have also constructed a runaway replication cds-plasmid that directs approximately 50-fold overproduction of CDP-diglyceride synthetase. This overproduction has been utilized in the purification of the enzyme to homogeneity, as described in the accompanying paper (Sparrow, C.P., and Raetz, C.R.H., J. Biol. Chem. 260, 12084-12091). Finally, the molecular cloning work reported herein allows the exact placement of the cds gene on the E. coli genetic map.
大肠杆菌的cds基因编码CDP - 二甘油酯合成酶。我们现在报告携带cds的质粒的构建。利用这些质粒,我们对1274个碱基对的DNA进行了测序,其中包括一个750个碱基对的开放阅读框,它是cds基因的编码区。该DNA序列使我们能够推断出CDP - 二甘油酯合成酶的初级肽序列。该蛋白质具有很强的疏水性,在不考虑加工或修饰的情况下,分子量为27,570。此外,在cds之后紧接着还有一个开放阅读框,这意味着cds可能是一个操纵子的一部分。我们还构建了一个失控复制的cds质粒,它能使CDP - 二甘油酯合成酶的产量提高约50倍。如随附论文(Sparrow, C.P., and Raetz, C.R.H., J. Biol. Chem. 260, 12084 - 12091)所述,这种过量表达已被用于将该酶纯化至同质状态。最后,本文报道的分子克隆工作使cds基因能够精确地定位在大肠杆菌的遗传图谱上。