Dilley R A, Nishiyama Y, Gombos Z, Murata N
Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907, USA.
J Bioenerg Biomembr. 2001 Apr;33(2):135-41. doi: 10.1023/a:1010752531909.
Fatty acid composition of the membrane lipids in the mesophilic cyanobacterium Synechocystis sp. PCC 6803 was altered in earlier work by targeted mutagenesis of genes for fatty acid desaturases. In this work, cells of several mutant strains, depleted in the unsaturated fatty acids in membrane lipids, were grown at 34 degrees C. Spheroplasts (permeabilized cells) were prepared by lysozyme digestion of the cell wall followed by gentle osmotic shock. The bioenergetic parameters ATP formation, electron transport, and H+ uptake were measured at various temperatures. All three bioenergetic parameters for spheroplasts from wild-type cells (which had abundant polyunsaturated fatty acids) were active down to the lowest temperatures used (1 degrees - 2 degrees C). In two strains, which lacked the capacity to desaturate fatty acids at the A 12 position and at the A 12 and A6 positions (designated as desA- and desA-/desD-, respectively), the spheroplasts lost the capacity to form ATP (measured as phenazine methosulfate cyclic phosphorylation) at about 5 degrees C but retained electron transport (water oxidation-dependent ferricyanide reduction) and H+ uptake linked to phenazine methosulfate cyclic electron transport. It appears that the absence of the unsaturation of fatty acids in the A 12 and A6 positions blocks the ability of the photosynthetic membranes to couple a bioenergetically competent proton-motive force to the ATP formation mechanism at temperatures below 5 degrees C. It remains to be determined whether the loss of ATP formation in the mutant strains is the failure of available protons to properly flow into the CF0CF1-ATP synthase or a failure in the CF1 part of the complex in coupling the dissipative H+ flow to the enzyme mechanism of the synthase.
在早期的研究中,通过对嗜温蓝藻集胞藻6803(Synechocystis sp. PCC 6803)中脂肪酸去饱和酶基因进行定向诱变,改变了其膜脂的脂肪酸组成。在本研究中,几种膜脂中不饱和脂肪酸含量降低的突变株细胞在34℃下培养。通过溶菌酶消化细胞壁,随后进行温和的渗透休克处理来制备原生质球(通透化细胞)。在不同温度下测量了生物能量参数ATP生成、电子传递和H⁺摄取。来自野生型细胞(具有丰富的多不饱和脂肪酸)的原生质球的所有这三个生物能量参数在所用的最低温度(1℃ - 2℃)下均具有活性。在两个分别缺乏在Δ¹²位置以及Δ¹²和Δ⁶位置使脂肪酸去饱和能力的菌株(分别命名为desA⁻和desA⁻/desD⁻)中,原生质球在约5℃时失去了形成ATP的能力(以吩嗪硫酸甲酯循环磷酸化来测量),但保留了电子传递(依赖水氧化的铁氰化物还原)以及与吩嗪硫酸甲酯循环电子传递相关的H⁺摄取。似乎在低于5℃的温度下,Δ¹²和Δ⁶位置脂肪酸缺乏不饱和度会阻碍光合膜将具有生物能量活性的质子动力与ATP形成机制相偶联的能力。突变株中ATP生成的丧失是由于可用质子未能正确流入CF₀CF₁ - ATP合酶,还是由于该复合物的CF₁部分在将耗散性H⁺流与合酶的酶促机制相偶联方面出现故障,仍有待确定。