Masukawa Hajime, Zhang Xiaohui, Yamazaki Emi, Iwata Syunsuke, Nakamura Kensuke, Mochimaru Mari, Inoue Kazuhito, Sakurai Hidehiro
Department of Biological Sciences, Kanagawa University, Hiratsuka, Kanagawa, Japan.
Mar Biotechnol (NY). 2009 May-Jun;11(3):397-409. doi: 10.1007/s10126-008-9156-z. Epub 2008 Nov 13.
As a first step toward developing the methodology for screening large numbers of heterocyst-forming freshwater cyanobacteria strains for the presence of various types of nitrogenases and hydrogenases, we surveyed the distribution of these genes and their activities in 14 strains from culture collections. The nitrogenase genes include nif1 encoding a Mo-type nitrogenase expressed in heterocysts, nif2 expressed in vegetative cells and heterocysts under anaerobic conditions, and vnf encoding a V-type nitrogenase expressed in heterocysts. Two methods proved to be valuable in surveying the distribution of nitrogenase types. The first method was Southern blot hybridization of DNA digested with two different endonucleases and hybridized with nifD1, nifD2, and vnfD probes. The second method was ethane formation from acetylene to detect the presence of active V-nitrogenase. We found that all 14 strains have nifD1 genes, and eight strains also have nifD2 genes. Four of the strains have vnfD genes, in addition to nifD2 genes. It is curious that three of these four strains had similar hybridization patterns with all of the nifD1, nifD2, and vnfD probes, suggesting that there could be some bias in strains used in the present study or in strains held in culture collections. This point will need to be assessed in the future. For surveying the distribution of hydrogenases, Southern blot hybridization was an effective method. All strains surveyed had hup genes, with the majority of them also having hox genes.
作为开发用于筛选大量形成异形胞的淡水蓝藻菌株中各种类型固氮酶和氢化酶方法的第一步,我们调查了这些基因在14种保藏菌株中的分布及其活性。固氮酶基因包括编码在异形胞中表达的钼型固氮酶的nif1、在厌氧条件下在营养细胞和异形胞中表达的nif2,以及编码在异形胞中表达的钒型固氮酶的vnf。事实证明,有两种方法在调查固氮酶类型分布方面很有价值。第一种方法是用两种不同的内切核酸酶消化DNA,并用nifD1、nifD2和vnfD探针进行杂交的Southern印迹杂交。第二种方法是通过乙炔形成乙烷来检测活性钒固氮酶的存在。我们发现所有14个菌株都有nifD1基因,8个菌株也有nifD2基因。除了nifD2基因外,其中4个菌株还有vnfD基因。奇怪的是,这4个菌株中的3个与所有nifD1、nifD2和vnfD探针都有相似的杂交模式,这表明本研究中使用的菌株或保藏菌株可能存在一些偏差。这一点未来需要评估。对于调查氢化酶的分布,Southern印迹杂交是一种有效的方法。所有被调查的菌株都有hup基因,其中大多数也有hox基因。