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Cloning and sequencing of nifBHDKENX genes of Paenibacillus massiliensis T7 and its nif promoter analysis
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作者 ZHAO Hongxin1,2,3, XIE Baoen2 & CHEN Sanfeng1,2 1. State Key Laboratory for Agrobiotechnology and Biological School, China Agricultural University, Beijing 100094, China 2. Key Laboratory for Agro-Microbial Resource and Application of Agriculture Ministry, China Agricultural University, Beijing 100094, China 3. Chemical and Biological School, ShenYang Normal University, Shenyang 110034, China 《Science China(Life Sciences)》 SCIE CAS 2006年第2期115-122,共8页
A 324 bp of nifH fragment was PCR amplified from Paenibacillus massiliensis T7 using the universal degenerate primers. The PCR-amplified nifH fragment was labeled with DIG; then used as a probe in Southern blot analys... A 324 bp of nifH fragment was PCR amplified from Paenibacillus massiliensis T7 using the universal degenerate primers. The PCR-amplified nifH fragment was labeled with DIG; then used as a probe in Southern blot analysis. Southern blot result showed that there were two positive signals, indicating that there might be two copies of nifH in P. massiliensis T7. A total of 10254 bp DNA sequence containing purD; nifBHDKENX was obtained by five rounds of inverse-PCR amplification. The predicted proteins of nifBHDKENX had high homology with those from other nitrogen-fixing bacteria. Only one putative σ[54]-dependent promoter sequence was detected upstream of the nifB gene; nifBHDKENX were likely to be organized in one operon. Assays of β-galactosidase activity of P. massiliensis T7PB carrying a nifB-lacZ fusion under different concentrations of NH4 [+]; O2 showed that the expression of nifB-lacZ was strongly inhibited by O2. 展开更多
关键词 PAENIBACILLUS massiliensis T7 nifBHDKENX nifB-lacZ inverse-pcr.
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