Poysti Nathan J, Oresnik Ivan J
Department of Microbiology, University of Manitoba, Winnipeg R3T 2N2, Manitoba, Canada.
J Bacteriol. 2007 May;189(9):3445-51. doi: 10.1128/JB.01707-06. Epub 2007 Mar 2.
A Tn5 mutant strain of Sinorhizobium meliloti with an insertion in tpiA (systematic identifier SMc01023), a putative triose phosphate isomerase (TPI)-encoding gene, was isolated. The tpiA mutant grew more slowly than the wild type on rhamnose and did not grow with glycerol as a sole carbon source. The genome of S. meliloti wild-type Rm1021 contains a second predicted TPI-encoding gene, tpiB (SMc01614). We have constructed mutations and confirmed that both genes encode functional TPI enzymes. tpiA appears to be constitutively expressed and provides the primary TPI activity for central metabolism. tpiB has been shown to be required for growth with erythritol. TpiB activity is induced by growth with erythritol; however, basal levels of TpiB activity present in tpiA mutants allow for growth with gluconeogenic carbon sources. Although tpiA mutants can be complemented by tpiB, tpiA cannot substitute for mutations in tpiB with respect to erythritol catabolism. Mutations in tpiA or tpiB alone do not cause symbiotic defects; however, mutations in both tpiA and tpiB caused reduced symbiotic nitrogen fixation.
分离得到了苜蓿中华根瘤菌(Sinorhizobium meliloti)的Tn5突变菌株,其在假定的磷酸丙糖异构酶(TPI)编码基因tpiA(系统标识符SMc01023)中存在插入。tpiA突变体在鼠李糖上的生长速度比野生型慢,并且不能以甘油作为唯一碳源生长。苜蓿中华根瘤菌野生型Rm1021的基因组包含第二个预测的TPI编码基因tpiB(SMc01614)。我们构建了突变体并证实这两个基因都编码功能性TPI酶。tpiA似乎是组成型表达的,并为中心代谢提供主要的TPI活性。已证明tpiB是利用赤藓糖醇生长所必需的。TpiB活性由利用赤藓糖醇生长诱导;然而,tpiA突变体中存在的TpiB活性基础水平允许利用糖异生碳源生长。虽然tpiA突变体可以被tpiB互补,但就赤藓糖醇分解代谢而言,tpiA不能替代tpiB中的突变。单独的tpiA或tpiB突变不会导致共生缺陷;然而,tpiA和tpiB两者的突变都会导致共生固氮减少