Philippot L, Clays-Josserand A, Lensi R, Trinsoutreau I, Normand P, Potier P
UMR CNRS 5557, Laboratoire d'Ecologie Microbienne du Sol, Université Claude Bernard, Lyon, Villeurbanne, France.
Biochim Biophys Acta. 1997 Feb 28;1350(3):272-6. doi: 10.1016/s0167-4781(97)00007-9.
The dissimilative membrane-bound nitrate reductase from Pseudomonas fluorescens strain AK15 was purified and the alpha subunit of the enzyme partially sequenced. On the basis of this partial amino acid sequence and of conserved stretches of amino acids between Escherichia coli and Bacillus subtilis, degenerate primers were design to amplify the narG gene and part of the narH gene in a PCR approach. The deduced amino acid sequence of narG shows 72% and 52% and narH 78% and 62% identity to the homologous subunit of E. coli and B. subtilis, respectively.
对荧光假单胞菌AK15菌株的异化型膜结合硝酸还原酶进行了纯化,并对该酶的α亚基进行了部分测序。基于此部分氨基酸序列以及大肠杆菌和枯草芽孢杆菌之间保守的氨基酸序列,设计了简并引物,采用聚合酶链反应(PCR)方法扩增narG基因和部分narH基因。推导的narG氨基酸序列与大肠杆菌和枯草芽孢杆菌同源亚基的同一性分别为72%和52%,narH的同一性分别为78%和62%。