NifA in Azospirillum brasilense plays a key role in regulating the synthesis and activity of nitrogenase in re- sponse to ammonia and oxygen available. In this work we used the yeast two-hybrid system to identify the ...NifA in Azospirillum brasilense plays a key role in regulating the synthesis and activity of nitrogenase in re- sponse to ammonia and oxygen available. In this work we used the yeast two-hybrid system to identify the proteins that interact with NifA. The nifA gene was fused to the yeast two-hybrid vector pGBD-C2, and three A. brasilense Sp7 genomic libraries for use in yeast two-hybrid studies were constructed. Screening of the libraries identified four clones encoding proteins that interact with NifA. The confirmation of the interactions of each gene product of the four clones and NifA were carried out by exchanging the vectors for nifA and the four clones and by mutageneses of the four clones with shift reading frame experiments in yeast two-hybrid studies. DNA sequence analyses showed that two clones en- code proteins containing PAS domains that play an impor- tant role in signal transduction. One clone has high similarity with the fhuE gene of Escherichia coli, whose gene product is involved in iron uptake and transportation, and the other clone encodes an unknown protein.展开更多
基金This work was supported by the National Basic Research Program of China(Grant No.2001CB108904)the Hi-Tech Research and Development Program of China(Grant No.2001AA214021).
基金supported by the National Natural Science Foundation of China(Grant No.30170020)by the Doctoral Fellowship of the Education Ministry of China(Grant No.20010019002).
文摘NifA in Azospirillum brasilense plays a key role in regulating the synthesis and activity of nitrogenase in re- sponse to ammonia and oxygen available. In this work we used the yeast two-hybrid system to identify the proteins that interact with NifA. The nifA gene was fused to the yeast two-hybrid vector pGBD-C2, and three A. brasilense Sp7 genomic libraries for use in yeast two-hybrid studies were constructed. Screening of the libraries identified four clones encoding proteins that interact with NifA. The confirmation of the interactions of each gene product of the four clones and NifA were carried out by exchanging the vectors for nifA and the four clones and by mutageneses of the four clones with shift reading frame experiments in yeast two-hybrid studies. DNA sequence analyses showed that two clones en- code proteins containing PAS domains that play an impor- tant role in signal transduction. One clone has high similarity with the fhuE gene of Escherichia coli, whose gene product is involved in iron uptake and transportation, and the other clone encodes an unknown protein.
