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铜绿假单胞菌PAO单链DNA结合蛋白的分离、测序及过量表达

Isolation, sequencing and overproduction of the single-stranded DNA binding protein from Pseudomonas aeruginosa PAO.

作者信息

Genschel J, Litz L, Thole H, Roemling U, Urbanke C

机构信息

Medizinische Hochschule, Hanover, Germany.

出版信息

Gene. 1996 Dec 5;182(1-2):137-43. doi: 10.1016/s0378-1119(96)00535-5.

Abstract

The gene (ssb) encoding the single-stranded DNA binding (SSB) protein from Pseudomonas aeruginosa PAO was detected on a 2.1 kbp PstI-fragment of chromosomal DNA. The protein (PaeSSB) encoded by this gene consists of 165 aa and has a M(r) of 18549. The genomic sequence was confirmed by amino acid sequencing of the amino terminus of SSB protein isolated from P. aeruginosa PAO. PaeSSB shows 68% homology to the respective protein of E. coli. The nucleotide sequence upstream of the P. aeruginosa ssb gene shows little homology to the regulatory region upstream of the ssb gene of E. coli. The ssb gene was located at a distance of 690-870 kbp from the origin of replication on a physical map of P. aeruginosa PAO. In vivo PaeSSB could replace the SSB protein of E. coli (EcoSSB) if its production was controlled by the lac promoter on a high-copy vector. PaeSSB was overproduced in E. coli. Both the overproduced protein and PaeSSB isolated from Pseudomonas aeruginosa PAO are post-translationally modified by cleavage of the first methionine. Analytical ultracentrifugation shows that PaeSSB is a stable homotetramer. The copy number of PaeSSB in P. aeruginosa is 1200 +/- 250 tetramers per cell. Preliminary characterization of the DNA binding properties shows PaeSSB to have a lower affinity for single-stranded DNA than EcoSSB.

摘要

从铜绿假单胞菌PAO中编码单链DNA结合(SSB)蛋白的基因(ssb),在染色体DNA的一个2.1 kbp的PstI片段上被检测到。该基因编码的蛋白(PaeSSB)由165个氨基酸组成,分子量为18549。通过对从铜绿假单胞菌PAO中分离的SSB蛋白的氨基末端进行氨基酸测序,证实了基因组序列。PaeSSB与大肠杆菌的相应蛋白具有68%的同源性。铜绿假单胞菌ssb基因上游的核苷酸序列与大肠杆菌ssb基因上游的调控区域几乎没有同源性。在铜绿假单胞菌PAO的物理图谱上,ssb基因位于距复制起点690 - 870 kbp处。在体内,如果PaeSSB的产生由高拷贝载体上的lac启动子控制,它可以替代大肠杆菌的SSB蛋白(EcoSSB)。PaeSSB在大肠杆菌中过量表达。从大肠杆菌中过量表达的蛋白以及从铜绿假单胞菌PAO中分离的PaeSSB在翻译后都通过切割第一个甲硫氨酸进行了修饰。分析超速离心表明PaeSSB是一种稳定的同四聚体。铜绿假单胞菌中PaeSSB的拷贝数为每个细胞1200±250个四聚体。对DNA结合特性的初步表征表明,PaeSSB对单链DNA的亲和力低于EcoSSB。

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