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1.
Chemosphere ; 87(10): 1171-8, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22397839

ABSTRACT

Bacterial communities in the rhizosphere soils of metal tolerant and accumulating Chenopodium ambrosioides grown in highly and moderately lead-zinc mine tailings contaminated-soils as well as the adjacent soils with low metal contamination were characterized by using cultivation-independent and cultivation techniques. A total of 69, 73, and 83 bacterial operational taxonomic units (OTUs) having 84.8-100% similarity with the closest match in the database were detected among high, moderate, and low-contamination soil clone libraries, respectively. These OTUs had a Shannon diversity index value in the range of 4.06-4.30. There were 9, 10, and 14 bacterial genera specific to high, moderate, and low metal-contaminated soil clone libraries, respectively. Phylogenetic analysis showed that the Pb-resistant isolates belonged to 8 genera. Pseudomonas and Arthrobacter were predominant among the isolates. Most of the isolates (82-86%) produced indole acetic acid and siderophores. More strains from the highly metal-contaminated soil produced 1-aminocyclopropane-1-carboxylate deaminase than the strains from the moderately and lowly metal-contaminated soils. In experiments involving canola grown in quartz sand containing 200 mg kg(-1) of Pb, inoculation with the isolated Paenibacillus jamilae HTb8 and Pseudomonas sp. GTa5 was found to significantly increase the above-ground tissues dry weight (ranging from 19% to 36%) and Pb uptake (ranging from 30% to 40%) compared to the uninoculated control. These results show that C. ambrosioides harbor different metal-resistant bacterial communities in their rhizosphere soils and the isolates expressing plant growth promoting traits may be exploited for improving the phytoextraction efficiency of Pb-polluted environment.


Subject(s)
Bacteria/isolation & purification , Bacteria/metabolism , Brassica rapa/growth & development , Brassica rapa/metabolism , Chenopodium ambrosioides/growth & development , Chenopodium ambrosioides/metabolism , Lead/pharmacology , Soil Pollutants/pharmacology , Bacteria/drug effects , Bacteria/genetics , Brassica rapa/microbiology , Carbon-Carbon Lyases/chemistry , Carbon-Carbon Lyases/pharmacology , Chenopodium ambrosioides/microbiology , China , Colony Count, Microbial , Indoleacetic Acids/metabolism , Lead/metabolism , Microbial Sensitivity Tests , Molecular Sequence Data , Phylogeny , Polymerase Chain Reaction , RNA, Ribosomal, 16S/genetics , Rhizosphere , Siderophores/metabolism , Soil Microbiology , Soil Pollutants/metabolism
2.
J Chem Ecol ; 34(9): 1213-8, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18679750

ABSTRACT

The antifungal activity of essential oil (EO) from the Brazilian epazote (Chenopodium ambrosioides L.) was evaluated by the poison food assay at concentrations of 0.3%, 0.1%, and 0.05% with eight postharvest deteriorating fungi (Aspergillus flavus, Aspergillus glaucus, Aspergillus niger, Aspergillus ochraceous, Colletotrichum gloesporioides, Colletotrichum musae, Fusarium oxysporum, and Fusarium semitectum). EO components were tentatively identified by Kováts retention indices (RIs) using gas chromatography and gas chromatography combined with mass spectrometry (GC-MS). Growth of all fungi was completely inhibited at 0.3% concentration, and by 90% to 100% at 0.1% concentration. The following 13 tentatively identified compounds (relative percent) accounted for 90.4% of the total volatile oil: alpha-terpinene (0.9), p-cymene (2.0), benzyl alcohol (0.3), p-cresol (0.3), p-mentha-1,3,8-triene (0.2), p-cimen-8-ol (0.6), alpha-terpineol (0.5), (Z)-ascaridole (61.4), piperitone (0.9), carvacrol (3.9), (E)-ascaridole (18.6), (E)-piperitol acetate (0.5), and (Z)-carvyl acetate (0.3). Autobiographic thin layer chromatography of the EO to separate the principal fungitoxic fraction yielded only one fraction that completely inhibited the growth of all test fungi at a concentration of 0.1%. This fraction was characterized by RIs and GC-MS presenting a composition (%) of p-cymene (25.4), (Z)-ascaridole (44.4), and (E)-ascaridole (30.2). The results suggest ascaridoles were the principal fungitoxic components of the EO.


Subject(s)
Antifungal Agents/pharmacology , Chenopodium ambrosioides/chemistry , Mitosporic Fungi/drug effects , Oils, Volatile/pharmacology , Plant Oils/pharmacology , Antifungal Agents/isolation & purification , Brazil , Chenopodium ambrosioides/growth & development , Food Contamination/prevention & control , Oils, Volatile/isolation & purification , Plant Leaves/chemistry , Plant Leaves/growth & development , Plant Oils/isolation & purification
3.
Chemotherapy ; 52(3): 130-6, 2006.
Article in English | MEDLINE | ID: mdl-16636536

ABSTRACT

BACKGROUND AND METHODS: Current therapy against leishmaniasis is unsatisfactory. Efficacious and safe new drugs are needed. In this study, we show the leishmanicidal effect of an essential oil from Chenopodium ambrosioides against Leishmania amazonensis. RESULTS: The tested product had a potent inhibitory action against promastigote and amastigote forms, with 50% effective dose values of 3.7 and 4.6 microg/ml, respectively. The essential oil showed a moderate toxicity on macrophages from BALB/c mice. An optimal dose of 30 mg/kg/day was effective when administered during 15 days by intraperitoneal route to BALB/c mice infected experimentally. CONCLUSION: These studies revealed a potential source for the discovery of novel drugs to combat the leishmaniasis based on the traditional medicine.


Subject(s)
Chenopodium ambrosioides/chemistry , Leishmania/drug effects , Leishmaniasis, Cutaneous/drug therapy , Oils, Volatile/pharmacology , Plant Oils/pharmacology , Animals , Chenopodium ambrosioides/growth & development , Cuba , Female , Injections, Intraperitoneal , Leishmania/physiology , Leishmaniasis, Cutaneous/parasitology , Macrophages/drug effects , Mice , Mice, Inbred BALB C , Oils, Volatile/administration & dosage , Oils, Volatile/isolation & purification , Plant Oils/administration & dosage , Plant Oils/isolation & purification
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