Motamedi H, Shafiee A
Department of Molecular Pharmacology and Biochemistry, Merck Research Laboratories, Rahway, New Jersey 07065, USA.
Eur J Biochem. 1998 Sep 15;256(3):528-34. doi: 10.1046/j.1432-1327.1998.2560528.x.
Biosynthesis of the macrolactone ring of FK506 involves 10 elongation cycles that mechanistically resemble the steps in fatty acid synthesis. Sequencing of a 40-kb DNA segment of the FK506 gene cluster from Streptomyces sp. MA6548 has revealed two additional polyketide synthases (PKS) genes fkbB and fkbC which lie upstream of fkbA, a PKS gene recently shown to be responsible for the last four condensation steps of the FK506 biosynthesis [Motamedi, H., Cai, S. J., Shafiee, A. & Elliston, K. O. (1997) Eur. J. Biochem. 244, 74-80]. fkbB and fkbC are contiguous and encode respectively, the first (790129 Da) and the second (374438 Da) components of the FK506 polyketide synthase, a complex of three multidomain polypeptides. The predicted domain structures of FkbB and FkbC are analogous to that of FkbA and comprise 30 fatty-acid-synthase(FAS)-like domains arranged in 6 modules. Each module performs a specific extension cycle in the assembly of the carbon skeleton of the FK506 macrolactone ring. The component activities for the initiation of the polyketide chain consisting of a dihydrocyclohexenylcarbonyl coenzyme A (CoA) synthetase and a dihydrocyclohexenylcarbonyl CoA reductase required for the formation of the dihydrocyclohexylcarbonyl CoA starter unit and an acyl-carrier-protein to which the starter unit is anchored and translocated to the appropriate site on the PKS multienzyme are located at the N-terminal region of the FkbB polypeptide. A third gene, fkbL, lies at one end of the cluster and encodes lysine cyclodeaminase which catalyzes alpha-deamination and cyclization of the lysine into pipecolate. A fourth gene fkbP located at the other end of the sequence reported here encodes a peptide synthetase required for the activation and incorporation of the pipecolate moiety into the completed acyl chain. Finally the cluster carries a gene, fkbO, whose product is presumed to carry out a post-polyketide oxidation step of the FK506 marocycle.
FK506大环内酯环的生物合成涉及10个延伸循环,其机制类似于脂肪酸合成的步骤。对链霉菌属MA6548的FK506基因簇的一个40kb DNA片段进行测序,发现了另外两个聚酮合酶(PKS)基因fkbB和fkbC,它们位于fkbA的上游,fkbA是一个PKS基因,最近被证明负责FK506生物合成的最后四个缩合步骤[Motamedi, H., Cai, S. J., Shafiee, A. & Elliston, K. O. (1997) Eur. J. Biochem. 244, 74 - 80]。fkbB和fkbC相邻,分别编码FK506聚酮合酶的第一个(790129 Da)和第二个(374438 Da)组分,FK506聚酮合酶是一种由三个多结构域多肽组成的复合物。FkbB和FkbC的预测结构域结构与FkbA类似,由6个模块中排列的30个脂肪酸合酶(FAS)样结构域组成。每个模块在FK506大环内酯环碳骨架的组装中执行特定的延伸循环。聚酮链起始所需的组分活性,包括二氢环己烯基羰基辅酶A(CoA)合成酶和二氢环己烯基羰基CoA还原酶,用于形成二氢环己基羰基CoA起始单元,以及一个酰基载体蛋白,起始单元锚定在该蛋白上并转移到PKS多酶的适当位点,这些活性位于FkbB多肽的N端区域。第三个基因fkbL位于基因簇的一端,编码赖氨酸环脱氨酶,该酶催化赖氨酸的α-脱氨和环化形成哌啶酸。这里报道的序列另一端的第四个基因fkbP编码一种肽合成酶,该酶是将哌啶酸部分激活并掺入完整酰基链所必需的。最后,该基因簇携带一个基因fkbO,其产物推测执行FK506大环的聚酮后氧化步骤。