José E. Ruiz-Sainz

The Sinorhizobium fredii HH103 Lipopolysaccharide is not only relevant at early soybean nodulation stages but also for symbiosome stability in mature nodules

In this work we have characterised the Sinorhizobium fredii HH103 greA lpsB lpsCDE genetic region and analysed for the first time the symbiotic performance of Sinorhizobium fredii lps mutants on soybean. The organization of the S. fredii HH103 greA, lpsB, and lpsCDE genes was equal to that of Sinorhizobium meliloti 1021. S. fredii HH103 greA, lpsB, and lpsE mutant derivatives produced altered LPS profiles that were characteristic of the gene mutated. In addition, S. fredii HH103 greA mutants showed a reduction in bacterial mobility and an increase of auto-agglutination in liquid cultures. RT-PCR and qPCR experiments demonstrated that the HH103 greA gene has a positive effect on the transcription of lpsB. Soybean plants inoculated with HH103 greA, lpsB or lpsE mutants formed numerous ineffective pseudonodules and showed severe symptoms of nitrogen starvation. However, HH103 greA and lps mutants were also able to induce the formation of a reduced number of soybean nodules of normal external morphology, allowing the possibility of studying the importance of bacterial LPS in later stages of the S. fredii HH103-soybean symbiosis. The infected cells of these nodules showed signs of early termination of symbiosis and lytical clearance of bacteroids. These cells also had very thick walls and accumulation of phenolic-like compounds, pointing to induced defense reactions. Our results show the importance of bacterial LPS in later stages of the S. fredii HH103-soybean symbiosis and their role in preventing host cell defense reactions. S. fredii HH103 lpsB mutants also showed reduced nodulation with Vigna unguiculata, although the symbiotic impairment was less pronounced than in soybean.

Sinorhizobium fredii HH103 mutants affected in capsular polysaccharide (KPS) are impaired for nodulation with soybean and Cajanus cajan.

The Sinorhizobium fredii HH103 rkp-1 region, which is involved in capsular polysaccharides (KPS) production, was isolated and sequenced. The organization of the S. fredii genes identified, rkpUAGHIJ and kpsF3, was identical to that described for S. meliloti 1021 but different from that of S. meliloti AK631. The long rkpA gene (7.5 kb) of S. fredii HH103 and S. meliloti 1021 appears as a fusion of six clustered AK631 genes, rkpABCDEF. S. fredii HH103-Rif(r) mutants affected in rkpH or rkpG were constructed. An exoA mutant unable to produce exopolysaccharide (EPS) and a double mutant exoA rkpH also were obtained. Glycine max (soybean) and Cajanus cajan (pigeon pea) plants inoculated with the rkpH, rkpG, and rkpH exoA derivatives of S. fredii HH103 showed reduced nodulation and severe symptoms of nitrogen starvation. The symbiotic capacity of the exoA mutant was not significantly altered. All these results indicate that KPS, but not EPS, is of crucial importance for the symbiotic capacity of S. fredii HH103-Rif(r). S. meliloti strains that produce only EPS or KPS are still effective with alfalfa. In S. fredii HH103, however, EPS and KPS are not equivalent, because mutants in rkp genes are symbiotically impaired regardless of whether or not EPS is produced.

Effect of pH and soybean cultivars on the quantitative analyses of soybean rhizobia populations

Quantitative analyses of fast- and slow-growing soybean rhizobia populations in soils of four different provinces of China (Hubei, Shan Dong, Henan, and Xinjiang) have been carried out using the most probable number technique (MPN). All soils contained fast- (FSR) and slow-growing (SSR) soybean rhizobia. Asiatic and American soybean cultivars grown at acid, neutral and alkaline pH were used as trapping hosts for FSR and SSR strains. The estimated total indigenous soybean-rhizobia populations of the Xinjiang and Shan Dong soil samples greatly varied with the different soybean cultivars used. The soybean cultivar and the pH at which plants were grown also showed clear effects on the FSR/SSR rations isolated from nodules. Results of competition experiments between FSR and SSR strains supported the importance of the soybean cultivar and the pH on the outcome of competition for nodulation between FSR and SSR strains. In general, nodule occupancy by FSRs significantly increased at alkaline pH. Bacterial isolates from soybean cultivar Jing Dou 19 inoculated with Xinjiang soil nodulate cultivars Heinong 33 and Williams very poorly. Plasmid and lipopolysaccharide (LPS) profiles and PCR-RAPD analyses showed that cultivar Jing Dou 19 had trapped a diversity of FSR strains. Most of the isolates from soybean cultivar Heinong 33 inoculated with Xinjiang soil were able to nodulate Heinong 33 and Williams showed very similar, or identical, plasmid, LPS and PCR-RAPD profiles. All the strains isolated from Xinjiang province, regardless of the soybean cultivar used for trapping, showed similar nodulation factor (LCO) profiles as judged by thin layer chromatographic analyses. These results indicate that the existence of soybean rhizobia sub-populations showing marked cultivar specificity, can affect the estimation of total soybean rhizobia populations indigenous to the soil, and can also affect the diversity of soybean rhizobial strains isolated from soybean nodules.

NolR Regulates Diverse Symbiotic Signals of Sinorhizobium fredii HH103

We have investigated in Sinorhizobium fredii HH103-1 (=HH103 Str(r)) the influence of the nolR gene on the production of three different bacterial symbiotic signals: Nod factors, signal responsive (SR) proteins, and exopolysaccharide (EPS). The presence of multiple copies of nolR (in plasmid pMUS675) repressed the transcription of all the flavonoid-inducible genes analyzed: nodA, nodD1, nolO, nolX, noeL, rhcJ, hesB, and y4pF. Inactivation of nolR (mutant SVQ517) or its overexpression (presence of pMUS675) altered the amount of Nod factors detected. Mutant SVQ517 produced Nod factors carrying N-methyl residues at the nonreducing N-acetyl-glucosamine, which never have been detected in S. fredii HH103. Plasmid pMUS675 increased the amounts of EPS produced by HH103-1 and SVQ517. The flavonoid genistein repressed EPS production of HH103-1 and SVQ517 but the presence of pMUS675 reduced this repression. The presence of plasmid pMUS675 clearly decreased the secretion of SR proteins. Inactivation, or overexpression, of nolR decreased the capacity of HH103 to nodulate Glycine max. However, HH103-1 and SVQ517 carrying plasmid pMUS675 showed enhanced nodulation capacity with Vigna unguiculata. The nolR gene was positively identified in all S. fredii strains investigated, S. xinjiangense CCBAU110, and S. saheli USDA4102. Apparently, S. teranga USDA4101 does not contain this gene.

Evaluation of the Symbiotic Properties of Rhizobium fredii in European Soils

Summary The symbiotic properties of different Rhizobium fredii strains were evaluated in a controlled environment growth chamber, greenhouse, and field conditions. R. fredii strains HH 102-2 and HH 103 showed to be as good soybean inoculants as Bradyrhizobium japonicum USDA 110 in three years (1987, 1988 and 1992) of field experiments in Spanish soils. Thus, it is concluded that these two R. fredii strains are valid soybean inoculants in Spanish soils which, as all European soils, are devoid of indigenous B. japonicum and R. fredii strains. Competition experiments in field conditions (1987) showed that R. fredii strains HH102-2 and HH 103-2 were more competitive than B. japonicum USDA 110-1 to nodulate soybean cv. Williams. Results of competition studies in greenhouse conditions using acid (pH 4.9), neutral (pH 6.6) and alkaline (pH 8.1) soils showed that in the acid soil B. japonicum strains USDA 110 and 3-15-b3 totally outcompeted R. fredii strain HH 103 to nodulate on cv. Williams. Conversely, in the alkaline soil the fast-growing strain occupied more than 80% of the nodules. These results indicate that the soil pH could be an important factor in determining the competitive success of R. fredii and B. japonicum for nodulating soybeans.

Soybean interactions with soil microbes, agronomical and molecular aspects

Soybean, Glycine max (L.) Merrill, is one of the most important food crops in the world. High soybean yields require large amounts of N fertilizers, which are expensive and can cause environmental problems. The industrial fixation of nitrogen accounts for about 50% of fossil fuel usage in agriculture. In contrast, biological fixation of N2 is a low-cost source of N for soybean cropping through the symbiotic association between the plant and soil bacteria belonging to the genera Bradyrhizobium and Sinorhizobium, which are collectively called “soybean rhizobia“. In general, symbiotic nitrogen fixation in crop legumes not only reduces fertilizer costs but also improves soil fertility through crop rotation and intercropping. Biological nitrogen fixation is due to symbioses between leguminous plants and species of Rhizobium bacteria. Replacing this natural N source by synthetic N fertilizers would cost around 10 billion dollars annually. Moreover, legume seed and foliage have a higher protein content than that of non-legumes, and this makes them desirable protein crops. There is a wide knowledge of the industrial elaboration and use of commercial soybean inoculants based on bradyrhizobia strains. At present, the technology to prepare different types of inoculants, either solid or liquid, is sufficiently developed to meet market requirements, although further research and investments are still required to improve the symbiotic efficacy of rhizobial inoculants. Inoculation of soybeans under field conditions has been successful in the USA, Brazil and Argentina, which are the world leaders in soybean cultivation in terms of acreage and grain yields. There are, however, limitations to a wider use of rhizobial inoculants: the size of indigenous soil rhizobial populations can prevent the successful use of inoculants in some particular areas. For example, many Chinese soils contain more than 105 soybean rhizobia per gram of soil, which imposes a serious barrier for nodule occupancy by the soybean rhizobia used as an inoculant. The use of inoculants based on soil bacteria other than rhizobia has also increased in the last decades. An example is the genus Azospirillum, which can be used for its capacity to increase plant growth and seed yields through different mechanisms, such as the production of plant hormones and the increase in phosphate uptake by roots. In addition, co-inoculation with Azospirillum and rhizobia enhances nodulation and nitrogen fixation. Although less developed, it is expected that inoculants based on mycorrhizal fungi will also play a relevant role in sustainable agriculture and forestry. In spite of any possible limitations, the use of inoculants appears compulsory in a frame of sustainable agriculture, which seeks to increase crop yields and nutrient-use efficiency while reducing the environmental costs associated with agriculture intensification. This review also summarizes some of the most relevant genetic aspects of soybean rhizobia in relation to their symbiosis with soybeans. They can be listed as follows: (1) legume roots exude flavonoids, which are able to activate the transcription of nodulation (nod, nol, noe) genes; (2) expression of nodulation genes results in the production and secretion of lipo-chitin oligosaccharide signal molecules, called LCOs or “Nod factors”, which activate nodule organogenesis in the legume root; (3) LCOs induce numerous responses of the legume roots, such as hair curling and the formation of nodule primordia in the inner or outer cortex; (4) the function of many soybean rhizobia nod genes is known and the chemical structure of the LCOs produced has been determined; (5) in addition to LCOs, different soybean rhizobia surface polysaccharides are required for the formation of nitrogenfixing nodules; (6) surface polysaccharides might act as signal molecules or could prevent plant defense reactions. Cyclic glucans, capsular polysaccharides and lipopolysaccharides appear to play relevant roles in the soybean nodulation process since rhizobial mutants affected in any of these surface polysaccharides are symbiotically impaired. Present knowledge of the molecular bases determining cultivar-strain specificity and nodule occupancy by soybean rhizobia competitors is clearly insufficient. This lack of information is a serious barrier for developing strategies aimed at improving nodulation and symbiotic nitrogen fixation of commercial inoculants. In spite of these difficulties, recent studies have shown that the signaling pathway involved in triggering nodule organogenesis is independent of that operating in bacterial entry through infection thread formation. Theses facts might offer new insights for improving symbiotic nitrogen fixation and also for the feasibility of transferring nodule organogenesis, a first step in expanding this symbiotic interaction into other agriculturally important species.

Genetic diversity of fast-growing rhizobia that nodulate soybean (Glycine max L. Merr)

The fast-growing Rhizobium sp. strain NGR234, isolated from Papua New Guinea, and 13 strains of Sinorhizobium fredii, isolated from China and Vietnam, were fingerprinted by means of RAPD, REP, ERIC and ARDRA. ERIC, REP and RAPD markers revealed a considerable genetic diversity among fast-growing rhizobia. Chinese isolates showed higher levels of diversity than those strains isolated from Vietnam. ARDRA analysis revealed three different genotypes among fast-growing rhizobia that nodulate soybean, even though all belonged to a subcluster that included Sinorhizobium saheli and Sinorhizobium meliloti. Among S. fredii rhizobia, two strains, SMH13 and HH303, might be representatives of other species of nitrogen-fixing organisms. Although restriction analysis of the nifD–nifK intergenic DNA fragment confirmed the unique nature of Rhizobium sp. strain NGR234, several similarities between Rhizobium sp. strain NGR234 and S. fredii USDA257, the ARDRA analysis and the full sequence of the 16S rDNA confirmed that NGR234 is a S. fredii strain. In addition, ARDRA analysis and the full sequence of the 16S rDNA suggested that two strains of rhizobia might be representatives of other species of rhizobia.

Genome Sequence of the Soybean Symbiont Sinorhizobium fredii HH103

Sinorhizobium fredii HH103 is a fast-growing rhizobial strain that is able to nodulate legumes that develop determinate nodules, e.g., soybean, and legumes that form nodules of the indeterminate type. Here we present the genome of HH103, which consists of one chromosome and five plasmids with a total size of 7.22 Mb.

Sinorhizobium fredii HH103 cgs mutants are unable to nodulate determinate- and indeterminate nodule-forming legumes and overproduce an altered EPS.

Sinorhizobium fredii HH103 produces cyclic beta glucans (CG) composed of 18 to 24 glucose residues without or with 1-phosphoglycerol as the only substituent. The S. fredii HH103-Rifr cgs gene (formerly known as ndvB) was sequenced and mutated with the lacZ-gentamicin resistance cassette. Mutant SVQ562 did not produce CG, was immobile, and grew more slowly in the hypoosmotic GYM medium, but its survival in distilled water was equal to that of HH103-Rifr. Lipopolysaccharides and K-antigen polysaccharides produced by SVQ562 were not apparently altered. SVQ562 overproduced exopolysaccharides (EPS) and its exoA gene was transcribed at higher levels than in HH103-Rifr. In GYM medium, the EPS produced by SVQ562 was of higher molecular weight and carried higher levels of substituents than that produced by HH103-Rifr. The expression of the SVQ562 cgsColon, two colonslacZ fusion was influenced by the pH and the osmolarity of the growth medium. The S. fredii cgs mutants SVQ561 (carrying cgs::Omega) and SVQ562 only formed pseudonodules on Glycine max (determinate nodules) and on Glycyrrhiza uralensis (indeterminate nodules). Although nodulation factors were detected in SVQ561 cultures, none of the cgs mutants induced any macroscopic response in Vigna unguiculata roots. Thus, the nodulation process induced by S. fredii cgs mutants is aborted at earlier stages in V. unguiculata than in Glycine max.

A Comparative Study of the Physiological Characteristics, Plasmid Content and Symbiotic Properties of Different Rhizobium fredii Strains

Summary Three of the new Rhizobium fredii strains (HH003, HH102 and HH103) isolated by Dowdle and Bohlool (1985) were investigated for their plasmid content, carbon nutritional patterns, salt tolerance and host-range and symbiotic efficiency with eight different legumes of the “cowpea cross-inoculation group”. The three R. fredii strains harbour nif structural genes, homologous to nif H, D, K, on large plasmids (ca. 200 Md). Their carbon nutritional patterns and salt tolerance were the same as those reported for the R. fredii strains isolated by Keyser et al. (1982a). All three strains formed nitrogen fixing nodules on Macroptilium atropurpureum, Cajanus cajan, Phaseolus aureus and Vigna unguiculata var unguiculata but failed to nodulate on Vigna unguiculata subsp. cylindrica and Vigna angularis. Vigna radiata and Psophocarpus tetragonolobus were very poorly nodulated by at least one of the three R. fredii strains.