Kleiner D, Fitzke E
Biochim Biophys Acta. 1981 Feb 20;641(1):138-47. doi: 10.1016/0005-2736(81)90577-0.
Clostridium pasteurianum is able to build up about 100-fold gradients of methylammonium across the cell membrane. Methylammonium enters the cell by means of a carrier as shown by the energy requirement, saturation kinetics and a pH profile with a narrow maximum between pH 6.2 and 6.8. The methyl ammonium transport (apparent Km = 150 microM, V = 100 mumol/min per g dry weight) is competitively inhibited by ammonium (apparent Ki = 9 microM). The low Ki value and the observation that methylammonium cannot serve as a carbon or nitrogen source for Cl. pasteurianum strongly indicate that ammonium rather than methylammonium is the natural substrate. Uncouplers and inhibitors of energy metabolism or of the membrane-bound ATPase inhibit transport. Cl. pasteurianum maintains a membrane potential (interior negative) in the range 80-130 mV. This membrane potential was identified as the energy source: the same agents that block transport also decrease the membrane potential, and artificial generation of a membrane potential (by addition of valinomycin to K+-loaded cells) induces concentrative uptake of methylammonium. Thus NH4+ (or CH3NH3+) must be the transported species. Digestion of the cell wall by lysozyme does not abolish the transport activity.
巴氏芽孢杆菌能够在细胞膜两侧建立约100倍的甲基铵梯度。甲基铵通过载体进入细胞,这从能量需求、饱和动力学以及pH曲线(在pH 6.2至6.8之间有一个狭窄的最大值)可以看出。甲基铵转运(表观Km = 150 μM,V = 100 μmol/分钟每克干重)受到铵的竞争性抑制(表观Ki = 9 μM)。低Ki值以及甲基铵不能作为巴氏芽孢杆菌的碳源或氮源这一观察结果强烈表明,铵而非甲基铵是天然底物。能量代谢或膜结合ATP酶的解偶联剂和抑制剂会抑制转运。巴氏芽孢杆菌维持80 - 130 mV范围内的膜电位(内部为负)。该膜电位被确定为能量来源:阻断转运的相同试剂也会降低膜电位,而人工产生膜电位(通过向加载钾离子的细胞中添加缬氨霉素)会诱导甲基铵的浓缩摄取。因此,NH4 +(或CH3NH3 +)必定是被转运的物质。溶菌酶消化细胞壁并不会消除转运活性。