Brown A J, Snyder F
J Biol Chem. 1983 Apr 10;258(7):4184-9.
Alkyldihydroxyacetone-P (alkyl-DHAP) synthase catalyzes the exchange of the fatty acid esterified to C-1 of the DHAP portion of acyl-DHAP for a fatty alcohol to form 1-O-alkyl-DHAP, the first ether-linked intermediate in ether lipid biosynthesis. Another characteristic of the reaction is the exchange of the pro-R hydrogen at C-1. We have investigated this hydrogen exchange using palmitoyl-[1-R-3H]DHAP and a 1000-fold purified preparation of alkyl-DHAP synthase. We found a small but significant pro-R hydrogen exchange in the absence of the co-substrate, fatty alcohol. When [14C]hexadecanol was added, the increase in pro-R 3H exchange was equal to the [14C]hexadecyl-DHAP formed. Addition of [14C]palmitic acid resulted in an increase in pro-R 3H exchange that matched the formation of [14C]palmitoyl-DHAP by the acyl exchange activity of alkyl-DHAP synthase. Furthermore, although whole microsomes contain at least two acyl hydrolases for acyl-DHAP, purified preparations of alkyl-DHAP synthase do not form DHAP from acyl-DHAP. These results are discussed with respect to data obtained from other laboratories using whole microsomes and in support of our proposed ping-pong mechanism for alkyl-DHAP synthase.
烷基二羟基丙酮 -P(alkyl -DHAP)合酶催化酰基 -DHAP中与DHAP部分C-1位酯化的脂肪酸与脂肪醇进行交换,形成1-O-烷基 -DHAP,这是醚脂生物合成中的首个醚键连接中间体。该反应的另一个特点是C-1位的前-R氢的交换。我们使用棕榈酰 -[1-R-³H]DHAP和1000倍纯化的烷基 -DHAP合酶制剂研究了这种氢交换。我们发现在没有共底物脂肪醇的情况下,存在少量但显著的前-R氢交换。当加入[¹⁴C]十六醇时,前-R ³H交换的增加量与形成的[¹⁴C]十六烷基 -DHAP量相等。加入[¹⁴C]棕榈酸导致前-R ³H交换增加,这与烷基 -DHAP合酶的酰基交换活性形成[¹⁴C]棕榈酰 -DHAP的量相匹配。此外,尽管完整的微粒体含有至少两种用于酰基 -DHAP的酰基水解酶,但纯化的烷基 -DHAP合酶制剂不会从酰基 -DHAP形成DHAP。结合其他实验室使用完整微粒体获得的数据对这些结果进行了讨论,并支持我们提出的烷基 -DHAP合酶的乒乓机制。