Tecoma E S, Sklar L A, Simoni R D, Hudson B S
Biochemistry. 1977 Mar 8;16(5):829-35. doi: 10.1021/bi00624a003.
The use of the fluorescent fatty acid, parinaric acid (9, 11, 13, 15-octadecatetraenoic acid) (PnA), was studied in cells of an unsaturated fatty acid auxotroph of Escherichia coli. Growth conditions were found that permitted biosynthetic incorporation of PnA (up to 3%) into membrane phospholipids during growth on oleic or elaidic acid. Fluorescence measurements of incorporated PnA revealed phase transitions in cells, membranes, and phospholipids at temperatures that reflected the fatty acid composition of the sample. Transitions had a well-defined onset from high temperature, while the lower and end point was less well defined. cis- and trans-PnA (cis, trnas, trans, cis, and all trans, respectively) gave comparable results. Similar phase transitions were detected with PnA, which was not biosynthetically incorporated. Fluorescence of tryptophan was measured in E. coli membranes as a function of concentration of PnA. Significant quenching of tryptophan fluorescence by PnA was observed.
研究了荧光脂肪酸——紫黄质酸(9,11,13,15 - 十八碳四烯酸)(PnA)在大肠杆菌不饱和脂肪酸营养缺陷型细胞中的应用。发现了一些生长条件,在油酸或反油酸上生长期间,这些条件允许PnA(高达3%)通过生物合成掺入膜磷脂中。对掺入的PnA进行荧光测量,结果显示在反映样品脂肪酸组成的温度下,细胞、膜和磷脂中发生了相变。相变从高温开始有明确的起始点,而较低温度和终点则不太明确。顺式和反式PnA(分别为顺式、反式、反式、顺式和全反式)给出了可比的结果。对于未通过生物合成掺入的PnA,也检测到了类似的相变。在大肠杆菌膜中测量了色氨酸荧光作为PnA浓度的函数。观察到PnA对色氨酸荧光有显著的淬灭作用。