Characterization and monitoring of selected rhizobial strains isolated from tree legumes in Thailand

Tree legume rhizobia were isolated from five tree legumes; Acacia auriculaformis Cunn., A. mangium Willd., Milletia leucantha Kurz., Pterocarpus indicus Willd., and Xylia xylocarpa Taub. grown in Thailand.Forty four highly effective rhizobial strains were selected on the basis of nitrogenase activity, number of nodules and plant biomass. The selected strains were characterized in both terms of physiology andgenetics. Most of the strains are slow grower and able to nodulate cowpea rather than soybean. In addition, IAA production could be detected only from few strains. When almost complete 16S rRNAsequences were analysed, the results indicated that most of the selected strains most likely belong to Bradyrhizobium elkanii and Bradyrhizobium sp. except strains AA67 and PT59 which most likely belong to B. japonicum. The nodule occupancy of selected strains in forest soil condition was investigated by using GUS reporter gene. The nodule occupancy is in the range of 63 - 100%. This suggests theappropriate strains should be produced as inoculum for further application in reforestation programmes in Thailand

Identification of salt-tolerant Sinorhizobium sp. strain BL3 membrane proteins based on proteomics.

Sinorhizobium sp. BL3 is a salt-tolerant strain that can fix atmospheric nitrogen in symbiosis with leguminous host plants under salt-stress conditions. Since cell membranes are the first barrier to environmental change, it is interesting to explore the membrane proteins within this protective barrier under salt stress. The protein contents of membrane-enriched fractions obtained from BL3 were analyzed by nanoflow liquid chromatography interfaced with electrospray ionization tandem mass spectrometry. A total of 105 membrane proteins were identified. These proteins could be classified into 17 functional categories, the two biggest of which were energy production and conversion, and proteins not in clusters of orthologous groups (COGs). In addition, a comparative analysis of membrane proteins between salt-stressed and non-stressed BL3 cells was conducted using a membrane enrichment method and off-line SCX fractionation coupled to nanoLC-MS/MS. These techniques would be useful for further comparative analysis of membrane proteins that function in the response to environmental stress