Fernández-Piñas F, Leganés F, Wolk C P
MSU-DOE Plant Research Laboratory, East Lansing 48824.
J Bacteriol. 1994 Sep;176(17):5277-83. doi: 10.1128/jb.176.17.5277-5283.1994.
Mutagenesis of Anabaena sp. strain PCC 7120 with a derivative of transposon Tn5 led to the isolation of a mutant strain, P6, in which heterocysts are not formed (A. Ernst, T. Black, Y. Cai, J.-M. Panoff, D. N. Tiwari, and C. P. Wolk, J. Bacteriol. 174:6025-6032, 1992). Reconstruction of the transposon mutation of P6 in the wild-type strain reproduced the phenotype of the original mutant. Analysis by pulsed-field gel electrophoresis localized the transposition at ca. 3.44 Mb on the physical map of the chromosome of wild-type Anabaena sp. The transposon was situated within an open reading frame (ORF), which we denote hetP, whose wild-type form was cloned and also sequenced. The predicted HetP protein was not found to show significant sequence similarity to other proteins. The mutation in strain P6 could be complemented by a clone of a fragment of wild-type DNA that includes hetP and at least one additional ORF 3' from hetP, but not by a clone that includes hetP as its only ORF. The latter clone proved highly toxic. The phenotype of the P6 mutant may, therefore, be due to a polar effect of the insertion of the transposon. Filaments of strain P6 and of the wild-type strain, when bearing the complementing fragment on a pDU1-based plasmid, showed an increased frequency of clustered heterocysts compared with that of the wild-type strain.
用转座子Tn5的衍生物对鱼腥藻属(Anabaena sp.)菌株PCC 7120进行诱变,导致分离出一个突变菌株P6,该菌株中不形成异形胞(A. 恩斯特、T. 布莱克、Y. 蔡、J.-M. 帕诺夫、D. N. 蒂瓦里和C. P. 沃尔克,《细菌学杂志》174:6025 - 6032,1992年)。在野生型菌株中重建P6的转座子突变重现了原始突变体的表型特征。通过脉冲场凝胶电泳分析将转座定位在野生型鱼腥藻属染色体物理图谱上约3.44 Mb处。转座子位于一个开放阅读框(ORF)内,我们将其命名为hetP,其野生型形式被克隆并测序。预测的HetP蛋白未发现与其他蛋白质具有显著的序列相似性。菌株P6中的突变可以被包含hetP以及hetP下游至少一个额外ORF的野生型DNA片段克隆所互补,但不能被仅包含hetP作为唯一ORF的克隆所互补。后一种克隆证明具有高毒性。因此,P6突变体菌株的表型可能是由于转座子插入的极性效应所致。当菌株P6和野生型菌株的丝状体在基于pDU1的质粒上携带互补片段时,与野生型菌株相比,它们显示出异形胞聚集频率增加。