Eriksson P O, Rilfors L, Wieslander A, Lundberg A, Lindblom G
Department of Physical Chemistry, University of Umeå, Sweden.
Biochemistry. 1991 May 21;30(20):4916-24. doi: 10.1021/bi00234a012.
The two dominant glucolipids in Acholeplasma laidlawii, viz., 1,2-diacyl-3-O-(alpha-D-glucopyranosyl)-sn-glycerol (MGlcDG) and 1,2-diacyl-3-O-[alpha-D-glucopyranosyl-(1----2)-O-alpha-D-glucopyranosyl ]- sn-glycerol (DGlcDG), have markedly different phase behavior. MGlcDG has an ability to form nonlamellar phases, whereas DGlcDG only forms lamellar phases. For maintenance of a stable lipid bilayer, the polar headgroup composition in A. laidlawii is metabolically regulated in vivo, in response to changes in the growth conditions [Wieslander et al. (1980) Biochemistry 19, 3650; Lindblom et al. (1986) Biochemistry 25, 7502]. To investigate the mechanism behind the lipid regulation, we have here studied bilayers of mixtures of unsaturated MGlcDG and DGlcDG, containing a small fraction of biosynthetically incorporated perdeuterated palmitic acid, with 2H NMR. The order-parameter profile of the acyl chains and an apparent transverse spin relaxation rate (R2) were determined from dePaked quadrupole-echo spectra. The order of the acyl chains in DGlcDG-d31 increases upon addition of protonated MGlcDG, whereas the order of MGlcDG-d31 decreases when DGlcDG is added. The variation of order with lipid composition is rationalized from simple packing constraints. R2 increases linearly with the square of the order parameter (S2) up to S approximately 0.14; then, R2 goes through a maximum and decreases. The increase in R2 with S2, as well as the magnitude of R2, is largest for pure MGlcDG-d31, smallest for DGlcDG-d31, and similar for mixtures with the same molar ratio of MGlcDG/DGlcDG but with the deuterium label on different lipids.(ABSTRACT TRUNCATED AT 250 WORDS)
莱氏无胆甾原体中的两种主要糖脂,即1,2 - 二酰基 - 3 - O -(α - D - 吡喃葡萄糖基) - sn - 甘油(MGlcDG)和1,2 - 二酰基 - 3 - O - [α - D - 吡喃葡萄糖基 -(1→2)- O - α - D - 吡喃葡萄糖基] - sn - 甘油(DGlcDG),具有明显不同的相行为。MGlcDG能够形成非层状相,而DGlcDG仅形成层状相。为维持稳定的脂质双层,莱氏无胆甾原体中的极性头部基团组成在体内会根据生长条件的变化进行代谢调节[维斯兰德等人(1980年)《生物化学》19卷,3650页;林德布洛姆等人(1986年)《生物化学》25卷,7502页]。为研究脂质调节背后的机制,我们在此用2H NMR研究了不饱和MGlcDG和DGlcDG混合物的双层,其中含有一小部分生物合成掺入的全氘代棕榈酸。从去包络四极回波光谱确定了酰基链的序参数分布和表观横向自旋弛豫率(R2)。加入质子化的MGlcDG后,DGlcDG - d31中酰基链的有序度增加,而加入DGlcDG时,MGlcDG - d31的有序度降低。根据简单的堆积限制对有序度随脂质组成的变化进行了合理化解释。R2随序参数(S2)的平方线性增加,直至S约为0.14;然后,R2达到最大值并下降。R2随S2的增加以及R2的大小,对于纯MGlcDG - d31最大,对于DGlcDG - d31最小,对于具有相同MGlcDG / DGlcDG摩尔比但氘标记在不同脂质上的混合物则相似。(摘要截断于250字)