Steenkamp D J, Peck H D
J Biol Chem. 1981 Jun 10;256(11):5450-8.
Proton translocation by Desulfovibrio desulfuricans cells, cultured anaerobically with nitrate as terminal oxidant, was studied by the oxidant-pulse method. Nitrate-grown D. desulfuricans translocated protons rapidly and reproducibly with hydrogen as reductant and nitrite as electron acceptor. H+/2e- ratios were typically in the range 1.8-2.2. Proton translocation following pulses of nitrite was also observed with endogenous substrate in freshly harvested cells and with lactate or formate as electron donors in starved cells. Problems in the determination of H+/2e- ratios when endogenous substrate, formate, or lactate was the electron donor are discussed. Evidence is presented for the location of formate dehydrogenase, hydrogenase, and nitrite reductase on the periplasmic and for lactate dehydrogenase on the cytoplasmic side of the cytoplasmic membrane.
采用氧化剂脉冲法,研究了以硝酸盐作为末端氧化剂进行厌氧培养的脱硫脱硫弧菌细胞的质子转运。以硝酸盐培养的脱硫脱硫弧菌,以氢气作为还原剂、亚硝酸盐作为电子受体时,能够快速且可重复地转运质子。H⁺/2e⁻ 比值通常在1.8 - 2.2范围内。在新鲜收获的细胞中,以内源底物作为电子供体,以及在饥饿细胞中以乳酸盐或甲酸盐作为电子供体时,也观察到了亚硝酸盐脉冲后的质子转运。讨论了以内源底物、甲酸盐或乳酸盐作为电子供体时,测定H⁺/2e⁻ 比值时存在的问题。有证据表明,甲酸脱氢酶、氢化酶和亚硝酸还原酶位于周质中,而乳酸脱氢酶位于细胞质膜的细胞质一侧。