Hoenke S, Wild M R, Dimroth P
Institut für Mikrobiologie der Eidgenössischen Technischen Hochschule Zürich, Schmelzbergstrasse 7, CH-8092 Zürich, Switzerland.
Biochemistry. 2000 Oct 31;39(43):13223-32. doi: 10.1021/bi0011532.
Malonate decarboxylase from Klebsiella pneumoniae consists of four subunits MdcA, D, E, and C and catalyzes the cleavage of malonate to acetate and CO(2). The smallest subunit MdcC is an acyl carrier protein to which acetyl and malonyl thioester residues are bound via a 2'-(5' '-phosphoribosyl)-3'-dephospho-CoA prosthetic group and turn over during the catalytic mechanism. We report here on the biosynthesis of holo acyl carrier protein from the unmodified apoprotein. The prosthetic group biosynthesis starts with the MdcB-catalyzed condensation of dephospho-CoA with ATP to 2'-(5' '-triphosphoribosyl)-3'-dephospho-CoA. In this reaction, a new alpha (1' ' --> 2') glycosidic bond between the two ribosyl moieties is formed, and thereby, the adenine moiety of ATP is displaced. MdcB therefore is an ATP:dephospho-CoA 5'-triphosphoribosyl transferase. The second protein involved in holo ACP synthesis is MdcG. This enzyme forms a strong complex with the 2'-(5' '-triphosphoribosyl)-3'-dephospho-CoA prosthetic group precursor. This complex, called MdcG(i), is readily separated from free MdcG by native polyacrylamide gel electrophoresis. Upon incubation of MdcG(i) with apo acyl carrier protein, holo acyl carrier protein is synthesized by forming the phosphodiester bond between the 2'-(5' '-phosphoribosyl)-3'-dephospho-CoA prosthetic group and serine 25 of the protein. MdcG corresponds to a 2'-(5' '-triphosphoribosyl)-3'-dephospho-CoA:apo ACP 2'-(5' '-phosphoribosyl)-3'-dephospho-CoA transferase. In absence of the prosthetic group precursor, MdcG catalyzes at a low rate the adenylylation of apo acyl carrier protein using ATP as substrate. The adenylyl ACP thus formed is an unphysiological side product and is not involved in the biosynthesis of holo ACP. The 2'-(5' '-triphosphoribosyl)-3'-dephospho-CoA precursor of the prosthetic group has been purified and its identity confirmed by mass spectrometry and enzymatic analysis.
肺炎克雷伯菌的丙二酸脱羧酶由四个亚基MdcA、D、E和C组成,催化丙二酸裂解为乙酸和二氧化碳。最小的亚基MdcC是一种酰基载体蛋白,乙酰基和丙二酰硫酯残基通过一个2'-(5''-磷酸核糖基)-3'-去磷酸辅酶A辅基与之结合,并在催化机制中周转。我们在此报告了从未修饰的脱辅基蛋白生物合成全酶酰基载体蛋白的过程。辅基生物合成始于MdcB催化的去磷酸辅酶A与ATP缩合生成2'-(5''-三磷酸核糖基)-3'-去磷酸辅酶A。在这个反应中,两个核糖基部分之间形成了一个新的α(1''→2')糖苷键,从而取代了ATP的腺嘌呤部分。因此,MdcB是一种ATP:去磷酸辅酶A 5'-三磷酸核糖基转移酶。参与全酶酰基载体蛋白合成的第二种蛋白质是MdcG。这种酶与2'-(5''-三磷酸核糖基)-3'-去磷酸辅酶A辅基前体形成一种强复合物。这种复合物称为MdcG(i),通过非变性聚丙烯酰胺凝胶电泳很容易与游离的MdcG分离。将MdcG(i)与脱辅基酰基载体蛋白一起温育时,通过在2'-(5''-磷酸核糖基)-3'-去磷酸辅酶A辅基与蛋白质的丝氨酸25之间形成磷酸二酯键来合成全酶酰基载体蛋白。MdcG相当于一种2'-(5''-三磷酸核糖基)-去磷酸辅酶A:脱辅基酰基载体蛋白2'-(5''-磷酸核糖基)-3'-去磷酸辅酶A转移酶。在没有辅基前体的情况下,MdcG以低速率催化使用ATP作为底物对脱辅基酰基载体蛋白进行腺苷酸化。由此形成的腺苷酰化酰基载体蛋白是一种非生理性副产物,不参与全酶酰基载体蛋白的生物合成。辅基的2'-(5''-三磷酸核糖基)-3'-去磷酸辅酶A前体已被纯化,并通过质谱和酶促分析确认了其身份。