A Gram-negative, non-motile, pale-yellow, rod-shaped bacterial strain, DS-42(T), was isolated from a soil in Korea and its taxonomic position was investigated by a polyphasic study. Strain DS-42(T) grew optimally at 25 degrees C and pH 7.0-8.0. Strain DS-42(T) did not form nodules on three different legumes, and the nodD and nifH genes were also not detected by PCR. Strain DS-42(T) contained Q-...

The early steps of symbiotic nodule formation by Rhizobium on plants require coordinate expression of several nod gene operons, which is accomplished by the activating protein NodD. Three different NodD proteins are encoded by Sym plasmid genes in Rhizobium meliloti, the alfalfa symbiont. NodD1 and NodD2 activate nod operons when Rhizobium is exposed to host plant inducers. The third, NodD3, is...

The pot experiments were conducted in the Department of Life Science and Bioinformatics of Assam University, Silchar. The aim of the present study was to investigate the effect of dual inoculation of Arbuscular mycorrhiza (AM) (Glomus fasciculatum) and Rhizobium on the chlorophyll, nitrogen and phosphorus contents of pigeon pea (Cajanus cajan L.). The results revealed an overall increase in chl...

In field peas, ascochyta blight is one of the most common fungal diseases caused by Didymella pinodes. Despite the high diversity of pea cultivars, only little resistance has been developed until to date, still leading to significant losses in grain yield. Rhizobia as plant growth promoting endosymbionts are the main partners for establishment of symbiosis with pea plants. The key role of Rhizo...

Minute 3. New taxa. New taxa described since the last meeting on 4 July 2001 are Bradyrhizobium yuanmingense Yao et al. [Int J Syst Evol Microbiol 52 (2002), 2219–2230], Bradyrhizobium betae Rivas et al. [Int J Syst Evol Microbiol 54 (2004), 1271–1275], Rhizobium indigoferae Wei et al. [Int J Syst Evol Microbiol 52 (2002), 2231–2239], Rhizobium loessense Wei et al. [Int J Syst Evol Microbiol 53...

We compared the nodulation competitiveness of three strains of Rhizobium leguminosarum by counting the number of nodules formed on faba bean plants after the application at sowing time of different concentrations of the strains to soils already containing Rhizobium strains of the same species. A relationship of type y = ax was found to exist between the ratio of the nodules formed by the applie...

Rhizobium-legume symbiosis begins with two free living organisms, and ends with an intimate cellular co-existence. Rhizobium bacteria recognize specific plants, provoke development of a root nodule, and invade the plant tissue. Eventually, the Rhizobium cell transfers itself into a host cell, surrounds itself with plant membrane, and arranges a nutrient exchange in which the bacteria brings fix...

A glyceollin I accumulation o f about 6000 pmol • mg dry weight, a tenfold increase above control root tissue, was found in one type o f nodule from Glycine max which had been infected with a fix~ strain (61-A-24) o f Rhizobium japonicum. In nodules infected with one other ineffective (ßx~) strain o f Rhizobium japonicum (RH 31-Marburg) or with two f i x + strains o f Rhizobium japonicum (61 -A...

Symbiotic rhizobium–legume interactions, such as root hair curling, rhizobial invasion, infection thread expansion, cell division and proliferation of nitrogen-fixing bacteroids, nodule formation, involve extensive membrane synthesis, lipid remodeling cytoskeleton dynamics. However, little is known about these membrane–cytoskeleton interfaces related genes. Here, we report the roles a major pho...