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Hydrocarbon contamination cause serious environmental damage and human health problems, therefore, to resolve this problem has been proposed diversely remediation techniques friendly with the environment i.e. bioaugmentation, biostimulation, natural attenuation and phytoremediation. Among options, the phytoremediation causes minimum alterations to soil, low cost, it has proved good efficiency and gained public acceptation. In the present study, the capacity of Mimosa pigra to restore a contaminated soil with both anthracene and phenanthrene was evaluated, along with the soil physicochemical changes due to both plant and contaminant presence in the soil. A silt-loam contaminated soil with 100 mg kg-1 (dry weight) anthracene and 200 mg kg-1 (dry weight) phenanthrene was used in all three treatments: Contaminated soil with M. pigra (C1), contaminated soil without M. pigra (C2), and not contaminated soil with M. pigra (C0) as control. After 70 days of experimentation both biomass and height of M. pigra was not affected due to soil contaminants. There was no difference among treatments for some physicochemical characteristics e.g. soil pH, electrolytic conductivity, soil-texture, and total nitrogen content throughout the experiment. M. pigra increased the soil water holding capacity after 50 and 70 days of the experiment, however, total organic carbon content was lower after 70 days compared to the control treatment. The higher contaminant removal rate was before 7 days of experimentation for all treatments. Anthracene and phenanthrene content were lower in treatments with the presence of M. pigra: 92% of phenanthrene and 80% of anthracene were removed in C1 while nearly 77% of phenanthrene and 60% of anthracene were removed in C2. This suggest a greater removal of contaminants using M. pigra. Total removal of contaminants was not achieved. However, M. pigra was able to accumulate both compounds, showing the M. pigra capability for bioremediation use in contaminated soils.

This work was conducted with the objective to evaluate the effect of vermicompost application on chemical characteristics, energetic parameters and amino acids profile of hybrid race corn grain cultivated under open-field and rained conditions. The experiment was accomplished under a randomized complete design with three repetitions. Three treatments were evaluated: 1) Maize after inoculation with a commercial mycorrhizal arbuscular fungi mixture (Tec Myc 60®) plus vermicompost (V+M); vermicompost (V) and chemical fertilization (CF). Starch content in grain was 1.9% higher in V+M treatment in comparison with chemical, whereas crude protein, ether extract, crude fiber, acid detergent fiber, neutral detergent fiber, total phosphorous and phytic phosphorous were not different between treatments. Energetic parameters were not different between three treatments. 17 amino acids were evaluated of wich only tryptophan, leucine, valine, histidine and aspartic acid were higher in CF and V treatments in comparison with V+M treatment. In conclusion, it is possible to cultivate maize using vermicompost as fertilizer because chemical characteristics, energetic parameters and amino acids profile in maize grain were not affected compared with the maize cultivated with vermicompost added with biofertilizers (V+M) or with corn cultivated with chemical fertilizers (CF).

The use of phytonanoparticles in agriculture could decrease the use of fertilizers and therefore decrease soil contamination, due to their size being better assimilated in plants. It is important to mention that the nanofertilizer is slow-releasing and improves plant physiological properties and various nutritional parameters. The influence of soil and foliar applications of phytonanoparticles of ZnO with the Moringa oleifera extract under three concentrations (25, 50, and 100 ppm) was evaluated on the cherry tomato crop (Solanum lycopersicum L.). Synthesis of the phytonanoparticles was analyzed with ultraviolet-visible spectroscopy (UV-Vis) and infrared transmission spectroscopy with Fourier transform (FT-IR), as well as the analysis with the dynamic light scattering (DLS) technique. The morphometric parameters were evaluated before and after the application of the nanoparticles. The minerals’ content of fruits was done 95 days after planting. Results showed that soil application was better at a concentration of 25 ppm of phytonanoparticles since it allowed the greatest number of flowers and fruits on the plant; however, it was demonstrated that when performing a foliar application, the fruit showed the highest concentrations for the elements Mg, Ca, and Na at concentrations of 511, 4589, and 223 mg kg−1, respectively.

The green iguana appears to be a carrier for bacteria causing gastrointestinal infections in humans. The presence of diarrheagenic E. coli (DEC) pathotypes, however, has not been studied in this reptile. The aim of the current work was to investigate the prevalence of DEC in the intestines of 240 captive green iguanas, their phylogenetic groups, and the antibiotic susceptibility profile. E. coli strains were isolated from 41.7% (N = 100/240) of the intestinal content of green iguanas. DEC strains was identified in 25.9% of the screened population and were detected in the majority (62%, p = 0.009) of those reptiles carrying E. coli strains. Among DEC strains, STEC strains carrying the stx1 gene were the most prevalent pathotype isolated (38.7%), followed by EAEC and ETEC (27.4% each). Genetic markers of DEC strains belonging to the EHEC pathotype were not detected. More than a half of DEC strains were classified into the Clade I-II phylogroup (64.5%), followed by the phylogroup A (14.5%). The antibiotic susceptibility method demonstrated that a high proportion of DEC strains were resistance, or non-susceptible, to carbenicillin, amikacin, and ampicillin. We conclude that the green iguana kept in captivity is a carrier of DEC strains bearing resistance to first-line antibiotics, including penicillins. Given the increase presence of the green iguana in Latin American households, these reptiles represent a potential source of transmission to susceptible humans and therefore a potential source of gastrointestinal disease.

The carrot is considered a model system in plant cell culture. Spray drying represents a widely used technology to preserve microorganisms, such as bacteria and yeasts. In germplasm conservation, the most used methods are freeze drying and cryopreservation. Therefore, the aim of this work was to evaluate the effect of spray drying on the viability and totipotency of somatic carrot cells. Leaf, root and stem explants were evaluated to induce callus with 2 mg/L of 2,4-dichlorophenoxyacetic acid (2,4-D). Calli obtained from the stem were cultivated in a liquid medium with 1 mg/L of 2,4-D. Cell suspensions were spray dried with maltodextrin-gum Arabic and maltodextrin-xanthan gum mixtures, two outlet air temperatures (50 and 60 °C) and 120 °C inlet air temperature. Results showed that carrot cells were viable after spray drying, and this viability remained for six months at 8 °C. The totipotency of the microencapsulated cells was proven. Cells that were not spray dried regenerated 24.6 plantlets, while the spray dried cells regenerated 19 plantlets for each gram of rehydrated powder. Thus, spray drying allowed researchers to obtain viable and totipotent cells. This work is the first manuscript that reported the spray drying of plant somatic cells.

Moringa oleifera is a highly versatile plant with potential use in the agro-food and biochemical industry. The goals of this study were to evaluate the effect of chemical fertilization and vermicompost on plant growth, and to analyze the metabolomic profile of M. oleifera crops cultivated over agricultural and native soils. The extracts were obtained from 90-day-old leaves via extraction with a hydroalcoholic mixture. Multivariate data analyses, such as principal component analysis (PCA) and partial least square-discriminant analysis (PLS-DA), were used to differentiate the distribution of leaf metabolites according to the soils or types of fertilizers used for the cultivation of Moringa oleifera. The results indicated that there was no significant effect on parameters such as plant height, root length and dry weight of leaves (p < 0.05). UPLC-ESI-MS/MS analysis of leaf extracts revealed a wide range of flavonoids, alkaloids and organic acids. The results of PCA and PLS-DA confirmed that the type of fertilizer had an effect on the metabolomic profile of M. oleifera leaves. The application of vermicompost induced changes in the metabolomic profile, but not in the morphometric variables of Moringa oleifera. These results are important for metabolite production via organic cultures and over different soil types in the industrialization of Moringa.

Mango (Mangifera indica L.) peel and pulp are a source of dietary fiber (DF) and phenolic compounds (PCs) that constituent part of the indigestible fraction (IF). This fraction reaches the colon and acts as a carbon and energy source for intestinal microbiota. The effect of mango IF on intestinal microbiota during colonic fermentation is unknown. In this study, the isolated IF of a novel ‘Ataulfo’ mango-based bar (snack) UV-C irradiated and non-irradiated (UVMangoB and MangoB) were fermented. Colonic fermentation occurred in vitro under chemical-enzymatic, semi-anaerobic, batch culture and controlled pH colonic conditions. Changes in the structure of fecal microbiota were analyzed by 16s rRNA gene Illumina MiSeq sequencing. The community´s functional capabilities were determined in silico. The MangoB and UVMangoB increased the presence of Faecalibacterium, Roseburia, Eubacterium, Fusicatenibacter, Holdemanella, Catenibacterium, Phascolarctobacterium, Buttiauxella, Bifidobacterium, Collinsella, Prevotella and Bacteroides genera. The alpha indexes showed a decrease in microbial diversity after 6 h of colonic fermentation. The coordinates analysis indicated any differences between irradiated and non-irradiated bar. The metabolic prediction demonstrated that MangoB and UVMangoB increase the microbiota carbohydrate metabolism pathway. This study suggests that IF of mango-based bar induced beneficial changes on microbial ecology and metabolic pathway that could be promissory to prevention or treatment of metabolic dysbiosis. However, in vivo interventions are necessary to confirm the interactions between microbiota modulating and intestinal beneficial effects.

In the present study, the hexane, acetone and methanol extracts of stem, branches and roots from Crotalaria longirostrata were evaluated for their antifungal activity against Fusarium sp., Fusarium verticillioides and Aspergillus flavus. The variables analyzed were inhibition halos, mycelial growth inhibition, sporulation and minimum inhibitory concentration. Phytochemical analysis revealed the presence of saponins, coumarins, anthrones, anthraquinones, flavonoids and alkaloids on different organic extracts. The hexane extract showed zones of inhibition between 6.3 and 10.5 mm. The mycelia growth and sporulation of A. flavus were reduced to 90% with methanol extract. The minimum inhibitory concentration values obtained with hexane extracts were 6.75 mg mL-1 and with methanol extracts were 50 and 25 mg mL-1 for Fusarium strains. This is the first study reporting of phytochemical composition and biological activity of C. longirostrata that could be used as a natural alternative to control in vitro of certain important pathogenic fungi.

Current protocols for Agave americana L. micropropagation have limited commercial application due to the low number of plants produced by explant. Indirect organogenesis could be an alternative, however is necessary to optimize plant growth regulators for plantlet number maximization. The objective of this work was to optimize 2,4-dicholorophenoxyacetic acid (2,4-D) and 6-benzyl adenine (BA) concentrations on the induction of A. americana embryogenic callus from apical meristem as explant for maximized the number of shoots per callus using a response surface experimental design. MS medium containing 30 g l-1 sucrose amended with 0.11,0.18, 0.45 or 2.26 μM 2,4-D, and 11.0, 22.0, 38.2 or 44.0 μM BA was used. Nine treatments with three repetitions was applied and number of shoots per callus were monitored after 4, 16, 20 and 36 weeks. In vitro rooting of shoot was done in MS medium added with indole butyric acid (IBA). A maximum number of plantlets per explant (74) was obtained with 2.26 μM of 2,4-D and 38.2 μM BA. In conclusion, the indirect organogenesis of A. americana L. could be an alternative for obtain plantlets for propagation commercial purposes

El objetivo del trabajo fue evaluar el efecto de dos hongos micorrízicos arbusculares (HMA) a diferentes concentraciones de fósforo sobre la sobrevivencia y el crecimiento de plántulas de pina {Ananas comosus (L.) Merr.) obtenidas por micropropagación. Las plántulas se multiplicaron masivamente en cultivos in vitro y se aclimataron gradualmente bajo un esquema de estrés por temperatura en tres etapas secuenciales. Los efectos de los HMA y el fósforo no fueron significativos sobre la sobrevivencia y la altura de las plántulas, sin embargo, Glomus claroideum estimuló que las plántulas tuvieran mayor número de hojas y peso seco. Los resultados sugieren que la altura de las plántulas fue mayor cuando fueron cultivadas con G. claroideum y 0,9 mM de fósforo.The objective of this work was to assess the effect of two arbuscular mycorrhizal fungi (AMF) at different phosphorus concentrations on survival and growth of pineapple {Ananas comosus (L.) Merr.) plantlets obtained for micropropagation. Plantlets were multiplied for in vitro cultures and were acclimatized under three sequential steps. The effects of AMF and phosphorus were not significant on plantlet survival and plantlet height, however Glomus claroideum stimulated that the plantlets were with higher leaves number and dry weight. The results demonstrated that plantlet growth was maximized with G claroideum and phosphorus 0.9 mM.

Background. Ardisia compressa Kunth, is a wild species native from tropical evergreen forests of Mexico, it produces fruits with phytochemical, ecological and dietary potencial. Its fruits are appreciated by people from local communities. However, in Mexico there are no studies that allow knowing the state of its phenotypic diversity. Objective. Characterize the morphological diversity of A. compressa populations from Chiapas state, Mexico. Methodology. Ninety individuals of nine wild populations of A. compressa were evaluated using 45 morphological traits (16 qualitative and 29 quantitative). The qualitative data were subjected to descriptive analysis and quantitative data were used in an analysis of variance (ANOVA) and finally the qualitative and quantitative data were analyzed simultaneously by means of a multivariate analysis with the Ward-MLM Method. Results. The qualitative traits showed phenotypic variability in the characteristics of leaf and fruit color. The quantitative data showed significant differences (P≤ 0.05) in all traits evaluated. The results of the principal component analysis (PCA) and cluster analysis (UPGMA) grouped the populations into three morphological groups differentiated by the similarity of the morphological traits of the populations and not by their geographical origin. Implications. The results in this study should be considered to implementing strategies of plant production and conservation of A. compressa. Conclusion. A wide phenotypic variability was found organized into three morphological groups defined base on characteristics of tree height, number of fruits, number of flowers and ratio of length to thickness leaf. The quantitative traits allowed us to observe the greatest morphological variability in the populations of A. compressa.

The effect of water deficit was determined on both in vitro and soil seedling as well as in cells in suspension of Agave americana L. In order to do the establishment of cells, the formation of callus was induced; for it two auxins were evaluated: 2,4-dichlorophenoxyacetic acid (2,4-D) and 4-mino-3,5,6-trichloropicolinic acid (picloram) at three concentrations (0.25, 0.5 and 0.75 mg L-1) in three explants (leaf, root and meristems) cultured in MS semisolid medium. The callogenesis response was related to the type and section of the explant, as well as the regulator used, and a cell suspension was established using 0.5 mg L-1 naphthaleneacetic acid (NAA) + 0.5 mg L-1 Benzylaminopurine (BAP). Seedlings were exposed to polyethyleneglycol (15% and 30% w/v) with a water potential of -0.87 and -2.67 MPa, respectively, under soil conditions. Water stress was applied through restricted irrigation. Fresh weight, root system growth, and chlorophyll concentration were some of the parameters that were affected by the effect of water deficit on A. americana L. Chlorophyll concentration values were significantly decreased by 15 at 30% PEG (19.6 SPAD units) compared to the control treatment. In in vitro plants, the highest concentration of proline was found in the roots, being the treatment with 30% polyethylene glycol where the highest concentration of this osmoregulator was obtained (62.5 mg g-1 DW). Under restricted irrigation conditions, an increase in proline concentration was observed both in the aerial part (2.2 μg 100 g-1 DW) and in the root system (1.8 μg 100 g-1 DW). However, the concentrations found were approximately ten times greater, less than those found under in vitro conditions. Therefore, the accumulation of proline can be considered an indicator of stress in Agave Americana L. growth in vitro. [ABSTRACT FROM AUTHOR]