Peters E P, Wilderspin A F, Wood S P, Zvelebil M J, Sezer O, Danchin A
ICRF Unit for Structural Molecular Biology, Birbeck College, London, UK.
Mol Microbiol. 1991 May;5(5):1175-81. doi: 10.1111/j.1365-2958.1991.tb01890.x.
The pyruvate-stimulated adenylate cyclase from Brevibacterium liquefaciens produces up to 450 microM cyclic AMP in the culture medium when the bacterium is grown on glucose and alanine. In this paper we report the cloning, expression and sequencing of the gene for this enzyme. Residues were identified, within the C-terminal domain, which are conserved in adenylate and guanylate cyclase sequences from eukaryotes and in the adenylate cyclase of the prokaryote Rhizobium meliloti. We have also identified a sequence of 30 residues near the N-terminus of the protein which is homologous to part of the regulatory domain of the cellular homologues of the oncogenes fes and fps; this sequence is also present in the avian Fujinami sarcoma virus fps gene.
当液化短杆菌在葡萄糖和丙氨酸上生长时,其丙酮酸刺激的腺苷酸环化酶在培养基中可产生高达450微摩尔的环腺苷酸。在本文中,我们报道了该酶基因的克隆、表达和测序。在C末端结构域内鉴定出了一些残基,这些残基在真核生物的腺苷酸和鸟苷酸环化酶序列以及原核生物苜蓿根瘤菌的腺苷酸环化酶中是保守的。我们还在该蛋白质的N末端附近鉴定出了一段30个残基的序列,该序列与癌基因fes和fps的细胞同源物的调节结构域的一部分同源;该序列也存在于禽富士纳美肉瘤病毒fps基因中。