Lehmicke L G, Lidstrom M E
J Bacteriol. 1985 Jun;162(3):1244-9. doi: 10.1128/jb.162.3.1244-1249.1985.
Mutants unable to grow on H2 and CO2 were isolated in the hydrogen-methanol autotroph Xanthobacter sp. strain H4-14 and complemented with a clone bank constructed in a broad-host-range cosmid vector. The mutants fell into two classes. Class I mutants (Cfx-) cannot grow on hydrogen or methanol and are deficient in one or more of the key enzymes of the Calvin Cycle. Class II mutants (Hox-) can grow on methanol but not on hydrogen and lack hydrogenase activity. Restriction maps of the complementing clones show that each class is not linked to the other. Subcloning and Tn5 mutagenesis have localized the regions of DNA complementing these mutants. The region complementing a class I mutant which is deficient in ribulosebisphosphate carboxylase activity is approximately 3.2 kilobase pairs in size. Expression of this enzyme activity from cloned DNA gave evidence for the orientation of an operon containing the structural genes for this enzyme. The region complementing most of the class II mutants is 3 to 4.5 kilobase pairs in size.
在氢-甲醇自养型黄色杆菌属菌株H4-14中分离出了不能在H2和CO2上生长的突变体,并用构建在广宿主范围黏粒载体中的克隆文库对其进行了互补。这些突变体分为两类。I类突变体(Cfx-)不能在氢气或甲醇上生长,并且在卡尔文循环的一种或多种关键酶中存在缺陷。II类突变体(Hox-)可以在甲醇上生长但不能在氢气上生长,并且缺乏氢化酶活性。互补克隆的限制性图谱表明,每一类都与另一类不连锁。亚克隆和Tn5诱变已确定了与这些突变体互补的DNA区域。与缺乏核酮糖二磷酸羧化酶活性的I类突变体互补的区域大小约为3.2千碱基对。从克隆DNA表达这种酶活性为包含该酶结构基因的操纵子的方向提供了证据。与大多数II类突变体互补的区域大小为3至4.5千碱基对。