“…Since the presence of a cyclopropane ring or a double bond on an acyl chain adjacent to the MPFA had little if any effect on the orientational ordering of the MFPA, it must be concluded that in the liquid-crystalline state the two fatty acyl chains experience a degree of independence sufficient to negate any influence of structural substitutents in one acyl chain upon the orientational order of the other. Previous 19F NMR results have demonstrated that the orientational order profiles of the MFPA chains in membranes of A. laidlawii B are highly similar in the liquid-crystalline state whether those membranes were enriched with straight-chain saturated fatty acids such as 15:0 (Macdonald et al, 1983(Macdonald et al, , 1985c 280, 290, 300, 310, and 320 K), or (D) 19:0 , 9 (240*, 250*, 260*, 270*, 280*, 280, 290, 300, and 310 K). The numbers in parentheses represent the temperatures at which the order profiles, from top to bottom, were acquired.…”