Efecto de bacterias emulsificantes en la atenuación de la fitotoxicidad de suelos contaminados con petróleo intemperizado / Effect of emulsifying bacteria on phytotoxicity attenuation of soils contaminated with weathered petroleum hydrocarbons

Introducción: Las plantas y los microorganismos se han utilizado como bioindicadores de la toxicidad inducida por hidrocarburos presentes en los suelos. Objetivo: El presente trabajo evaluó la toxicidad de un Gleysol contaminado de origen con diferentes concentraciones de petróleo intemperizado, recolectado en la Venta Tabasco (México), en el crecimiento de Clitoria ternatea, y la atenuación de la fitotoxicidad con la inoculación de bacterias emulsificantes. Metodología: Se usaron suelos con 50 y 150 g HTPI kg-1, y un suelo testigo con 0.15 g HTPI kg-1 (origen biogénico), y la inoculación de seis bacterias emulsificantes y su combinación (consorcio). La fitotoxicidad de los HTPI se evaluó considerando la altura, la biomasa seca (radical, aérea y total), el área foliar, el área foliar específica, y la eficiencia del fotosistema II (EPSII), a los 30 días. Resultados: Los HTPI no afectaron la altura, pero el suelo con 50 g HTPI kg-1 redujo la biomasa seca radical y total, y el área foliar con respecto a las plantas en los suelos testigo y con 150 g HTPI kg-1. La cepa Sml (Stenotrophomonas maltophilia C10S1) incrementó significativamente la biomasa seca total; la cepa Ro (Raoultella ornithinolyticaC5S3) produjo mayor área foliar específica con respecto a plantas no inoculadas. En el suelo testigo, el consorcio bacteriano estimuló la altura; las cepas Sm (Serratia marcescens C11S1) y Sm2 (S. marcescens C7S3) mejoraron la altura y el área foliar específica con respecto a plantas no inoculadas, en el suelo con 50 g HTPI kg-1. En el suelo con 150 g HTPI kg-1, las cepas Spa (Stenotrophomonas pavanii C5S3F) y Cfr (Citrobacter freundii C4S3) incrementaron la biomasa seca radical y aérea, respectivamente. La EPSII no fue afectada por la contaminación de los suelos. Las bacterias emulsificantes redujeron la fitotoxicidad de HTPI, pero dependiendo de su contenido en los suelos. Conclusiones: El suelo con 50 g HTPI kg-1 mostró mayor toxicidad en el crecimiento de las plantas. La inoculación bacteriana favoreció el crecimiento, producción de biomasa, y área foliar en el suelo con 150 g HTPI kg-1. La EPSII no fue afectada por la presencia de HTPI en el suelo.

Introduction: Plants and microorganisms have been used as bioindicators to evaluate the toxicity of hydrocarbons in soils. Objective: This study evaluates the toxicity of a chronically-contaminated Gleysol with several concentrations of weathered petroleum hydrocarbons (WPH), collected from La Venta, Tabasco (Mexico), on the growth of Clitoria ternatea and the phytoxicity attenuation due to inoculation of emulsifying bacteria. Methods: Soils with 50 and 150 g WPH kg-1, and control soil with 0.15 g WPH kg-1 (biogenic origin) were utilized, as well as the inoculation of six emulsifying bacteria and their combination (consortium). The WPH-phytotoxicity was evaluated by considering plant height, dry biomass production (root, shoot, and total), leaf area, specific leaf area, and the efficiency of photosystem II (EPSII), after 30 days. Results: WPH did not affect plant height, but soil with 50 g WPH kg-1 diminished root and total dry weight, and leaf area, when compared to both control soil and soil with 150 g WPH kg-1. The strain Sml (Stenotrophomonas maltophilia C10S1) significantly increased shoot and total dry weight, while the strain Ro (Raoultella ornithinolytica C5S3) produced higher specific leaf area relative to uninoculated plants. In control soil, the bacterial consortium stimulated plant height. The strains Sm (Serratia marcescens C11S1)and Sm2 (S. marcescens C7S3) improved plant height and specific leaf area when compared to uninoculated plants in soil with 50 g WPH kg-1. In soil with 150 g WPH kg-1, strains Spa (Stenotrophomonas pavanii C5S3F)and Cfr (Citrobacter freundii C4S3)enhanced root and shoot dry weight, respectively. The EPSII was unaffected by soil contamination. Emulsifying bacteria reduced the phytotoxic effects of WP, but depending on the content of WPH in soils. Conclusions: Soil with 50 g WPH kg-1 showed the greatest phytotoxic effects on plant growth. Bacterial inoculation favored growth, biomass production and leaf area in soil with 150 g WPH kg-1. The EPSII was not affected by WPH in soils.

Endophytic bacteria promote growth of the medicinal legume Clitoria ternatea L. by chemotactic activity.

Part of the native root nodule endophytic microflora referring to members of the genera Proteobacteria and Sphingobacteria were used to test their bioefficacy as seed biopriming. These were quantified for their plant growth promoting (PGP) attributes such as IAA production, P and K-solubilization and ACC deaminase production. Results showed that significantly highest IAA was produced by E. hormaechi RCT10. The highest P-solubilization was observed with S. maltophila RCT31 it was solubilizing all the substrate tri-calcium phosphate, di-calcium phosphate, and zinc phosphate. Significantly highest K-solubilization was observed with S. maltophila RCT31 followed by E. turicensis RCT5. However, the maximum zinc solubilization was reported with S. maltophila RCT31 followed by E. turicensis RCT5. The maximum ACC deaminase was quantified in the bacterium. Results revealed that the E. hormaechi RCT10 utilized seed leechates most effectively while root exudates were maximally utilized by S. maltophila RCT31. The pots experiment proves that S. maltophila RCT31 was the most effective bacterium and it was replication vis-à-vis field experiment. In particular, S. maltophila RCT31 holds strong potential to be possibly used as a bioformulation for the medicinal legume, as an economical and eco-friendly alternative to agrochemicals.

Inoculated Clitoria ternatea with Bacillus cereus ERBP for enhancing gaseous ethylbenzene phytoremediation: Plant metabolites and expression of ethylbenzene degradation genes.

Air pollutants especially polyaromatic hydrocarbons pose countless threats to the environment. This issue demands for an effective phytoremediation technology. In this study we report the beneficial interactions of Clitoria ternatea and its plant growth promoting endophytic bacteria Bacillus cereus ERBP by inoculating it for the remediation of 5 ppm airborne ethylbenzene (EB). The percentage efficiency for ethylbenzene removal among B. cereus ERBP inoculated and non-inoculated sterile and natural C. ternatea has also been determined. The inoculation of B. cereus ERBP has significantly increased EB removal efficiency of both sterile and natural C. ternatea. The inoculated natural C. ternatea seedlings showed 100% removal efficiency within 84 h for the aforementioned pollutant compared with the sterile inoculated C. ternatea seedlings (108 h). The degradation of EB by C. ternatea seedlings with and without B. cereus ERBP was assessed by measuring the intermediates of EB including 1-phenylethanol, acetophenon, benzaldehyde and benzoic acid. In addition, cytochrome P450s monooxygenase (CYP83D1) and dehydrogenases (LOC100783159) involved in the oxidation of hydrocarbons are well reported for their bio catalytic activities under xenobiotic stress conditions. Hence, the co-effect of the native endophyte B. cereus ERBP inoculation and EB exposure on the expression level of CYP83D1 and dehydrogenase were also determined. The targeted genes CYP83D1and dehydrogenases have shown an increased expression level under the 5 ppm of EB exposure enabling C. ternatea to withstand and remediate the pollutant.

Root nodule bacteria from Clitoria ternatea L. are putative invasive nonrhizobial endophytes.

In this study, bacteria (8 species and 5 genera) belonging to the classes Betaproteobacteria, Gammaproteobacteria, and Sphingobacteria were isolated from root nodules of the multipurpose legume Clitoria ternatea L. and identified on the basis of partial 16S rRNA sequencing. The root nodule bacteria were subjected to phenotypic clustering and diversity studies using biochemical kits, including Hi-Media Carbokit™, Enterobacteriaceae™ identification kit, ERIC-PCR, and 16S ARDRA. All the strains showed growth on Ashby's N-free media over 7 generations, indicative of presumptive nitrogen fixation and further confirmed by amplification of the nifH gene. None of the strains showed the capability to renodulate the host plant, neither alone nor in combination with standard rhizobial strains, which was further confirmed by the absence of nodC bands in PCR assay. The results clearly indicate the common existence of nonrhizobial microflora inside the root nodules of legumes, which were thought to be colonized only by rhizobia and were responsible for N2 fixation in leguminous crops. However, with the recent discovery of nodule endophytes from a variety of legumes, as also observed here, it can be assumed that symbiotic rhizobia are not all alone and that these invasive endophytes belonging to various bacterial genera are more than just opportunistic colonizers of specialized nodule niche.

Hairy root cultures of butterfly pea (Clitoria ternatea L.): Agrobacterium × plant factors influencing transformation.

Transformed rhizoclones were developed from Agrobacterium-treated explants of the medicinally important twinning legume Clitoria ternatea L. Several key factors influencing transformation events were optimized. A4T was the most infectious among the strains employed. Internode segments were more responsive than leaves, outdoor-grown explants preferred to those from in vitro cultures. High frequency transformation, resulting in up to 85.8% rhizogenesis, was attained using pre-pricked internodal explants for immersion (10 min) in Agrobacterium rhizogenes suspension grown overnight with acetosyringone (100 µM) to an OD(660) â‰… 0.6, diluted to a density of 10(9) cells ml(-1), followed by 5-day co-cultivation. Roots were individually cultured in MS0 supplemented with the bacteriostatic antibiotic cefotaxime (500 µg ml(-1)). Rhizoclones were renewed through successive subcultures in MS0 under diffused illumination. The T ( L )-DNA rolB and rolC ORF were detected in rhizoclones through PCR amplification. The T ( R )-DNA gene encoding mannopine synthase (man2) was revealed by positive amplification and opine gene expression substantiated by agropine and mannopine biosynthesis in all selected transformed rhizoclones. The implication of such findings is discussed on the context of utilization of such genetically transformed root cultures towards sustainable production of medicinally useful phytocompounds, besides providing a means for plant conservation.

Mesorhizobium thiogangeticum sp. nov., a novel sulfur-oxidizing chemolithoautotroph from rhizosphere soil of an Indian tropical leguminous plant.

The bacterial strain SJT(T), along with 15 other mesophilic, neutrophilic and facultatively sulfur-oxidizing chemolithotrophic isolates, was isolated by enrichment on reduced sulfur compounds as the sole energy and electron source from soils immediately adjacent to the roots of Clitoria ternatea, a slender leguminous herb of the Lower Gangetic plains of India. Strain SJT(T) was able to oxidize thiosulfate and elemental sulfur for chemolithoautotrophic growth. 16S rRNA and recA gene sequence-based phylogenetic analyses showed that the Gram-negative rod-shaped bacterium belonged to the genus Mesorhizobium and was most closely related to Mesorhizobium loti, Mesorhizobium plurifarium, Mesorhizobium amorphae and Mesorhizobium chacoense. Unequivocally low 16S rRNA (<97 %) and recA (< or =88 %) gene sequence similarities to all existing species of the most closely related genera, a unique fatty acid profile, a distinct G+C content (59.6 mol%) and phenotypic characteristics all suggested that strain SJT(T) represents a novel species. DNA-DNA hybridization and SDS-PAGE analysis of whole-cell proteins also confirmed the taxonomic uniqueness of SJT(T). It is therefore proposed that isolate SJT(T) (= LMG 22697T = MTCC 7001T) be classified as the type strain of a novel species, Mesorhizobium thiogangeticum sp. nov.