Chau MyDoanh, Walker Kevin, Long Robert, Croteau Rodney
Institute of Biological Chemistry, Washington State University, Pullman 99164-6340, USA.
Arch Biochem Biophys. 2004 Oct 15;430(2):237-46. doi: 10.1016/j.abb.2004.07.013.
In addition to the anticancer drug Taxol, yew (Taxus) species produce a large variety of other taxane diterpenoids which differ mainly in the type of acyl and aroyl groups appended to the many hydroxyl functions on the taxane core; acetate esters are particularly common. Taxol bears an acetate at C10 and another at C4 thought to originate by intramolecular migration of a C5 acetate function in the process of oxetane ring formation, but many other naturally occurring taxoids bear acetate groups at C1, C2, C7, C9, and C13, in addition to C5 and C10. cDNAs encoding a taxoid 5alpha-O-acetyltransferase (taxadien-5alpha-ol as substrate) and a taxoid 10beta-O-acetyltransferase (10-deacetylbaccatin III as substrate) have been acquired from a recently isolated family of Taxus acyl/aroyltransferase clones. To explore the origins of other acetylated taxoids, the group of recombinant Taxus acyltransferases was investigated with a range of polyhydroxylated taxoids as substrates. From this survey, a new acetyltransferase clone (denoted TAX19) was identified that was capable of acetylating taxadien-5alpha-ol with activity comparable to that of the previously identified 5alpha-O-acetyltransferase (clone TAX1). However, when these two recombinant enzymes were presented with taxadien-triol and tetraol substrates, they exhibited different regiospecificities. The TAX1 enzyme preferentially acetylates the "northern" hemisphere hydroxyls at C9 and C10, whereas the TAX19 enzyme preferentially acetylates the "east-west" pole positions at C5 and C13. The TAX1 enzyme possesses the lowest KM value with taxadien-5alpha-ol (an early pathway metabolite) as substrate, with much higher KM values for the polyhydroxylated taxoid substrates, whereas the TAX19 enzyme possesses lower KM values (than the TAX1 transferase) for all taxoid substrates tested. These results suggest that both TAX1 and TAX19 acyltransferases may function at the early C5 acetylation step of taxoid metabolism, and that the TAX19 acyltransferase, because of its broader specificity for polyhydroxylated taxoids, may also function later in metabolism and be responsible for the production of many other acetylated taxoids.
除了抗癌药物紫杉醇外,红豆杉属植物还能产生多种其他紫杉烷二萜类化合物,它们的主要区别在于紫杉烷核心上众多羟基所连接的酰基和芳酰基的类型;乙酸酯尤其常见。紫杉醇在C10位有一个乙酸酯,在C4位还有一个,据认为这是在氧杂环丁烷环形成过程中由C5位乙酸酯官能团分子内迁移产生的,但许多其他天然存在的紫杉烷类化合物除了在C5和C10位有乙酸酯基团外,在C1、C2、C7、C9和C13位也有。编码紫杉烷5α-O-乙酰转移酶(以紫杉二烯-5α-醇为底物)和紫杉烷10β-O-乙酰转移酶(以10-去乙酰巴卡亭III为底物)的cDNA已从最近分离的红豆杉酰基/芳酰基转移酶克隆家族中获得。为了探究其他乙酰化紫杉烷类化合物的来源,研究人员以一系列多羟基化紫杉烷类化合物为底物,对重组红豆杉酰基转移酶进行了研究。通过这项研究,鉴定出了一种新的乙酰转移酶克隆(命名为TAX19),它能够乙酰化紫杉二烯-5α-醇,其活性与先前鉴定的5α-O-乙酰转移酶(克隆TAX1)相当。然而,当用紫杉二烯三醇和四醇底物处理这两种重组酶时,它们表现出不同的区域特异性。TAX1酶优先乙酰化C9和C10位的“北半球”羟基,而TAX19酶优先乙酰化C5和C13位的“东西极”位置。以紫杉二烯-5α-醇(一种早期途径代谢物)为底物时,TAX1酶的KM值最低,而对于多羟基化紫杉烷类底物,其KM值要高得多,而对于所有测试的紫杉烷类底物,TAX19酶的KM值(比TAX1转移酶)更低。这些结果表明,TAX1和TAX19酰基转移酶可能都在紫杉烷类化合物代谢的早期C5乙酰化步骤中起作用,并且TAX19酰基转移酶由于对多羟基化紫杉烷类化合物具有更广泛的特异性,可能在代谢后期也起作用,并负责许多其他乙酰化紫杉烷类化合物的产生。