The full UHPLC-MS metabolome fingerprinting and anti- effect of (Molina) Mirb. (Nalca) total extract (GTE) and fractions prepared from its edible fresh petioles were evaluated. The activity of against strains ATCC 45504 and J99 was assessed by means of agar diffusion assay, Minimum Inhibition Concentration (MIC), and Minimum Bactericidal Concentration (MBC), while killing curve and transmission electronic microscopy (TEM) were conducted in order to determine the effect of the plant extract on bacterial growth and ultrastructure. Additionally, the inhibitory effect upon urease was evaluated using both the Jack Bean and enzymes. To determine which molecules could be responsible for the antibacterial effects, tentative identification was done by ultra-high performance liquid chromatography coupled with high-resolution mass spectrometry (UHPLC-Q-Orbitrap®-HR-MS). Furthermore, the total extract was fractionated using centrifugal partition chromatography (CPC), giving four active fractions (1-4). It was determined that the crude extract and centrifugal partition chromatography fractions of have a bactericidal effect being the lowest MIC and MBC = 32 μg/ml. In the killing curves, fraction one acts faster than control amoxicillin. In the urease assay, F3 exhibited the lowest IC value of 13.5 μg/ml. Transmission electronic microscopy showed that crude extract promotes disruption and separation of the cellular wall and outer membrane detachment on causing bacterial cell death.
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http://dx.doi.org/10.3389/fphar.2020.583961 | DOI Listing |
Front Pharmacol
January 2021
Laboratorio de Farmacognosia, Departamento de Farmacia, Facultad de Farmacia, Universidad de Concepción, Concepción, Chile.
The full UHPLC-MS metabolome fingerprinting and anti- effect of (Molina) Mirb. (Nalca) total extract (GTE) and fractions prepared from its edible fresh petioles were evaluated. The activity of against strains ATCC 45504 and J99 was assessed by means of agar diffusion assay, Minimum Inhibition Concentration (MIC), and Minimum Bactericidal Concentration (MBC), while killing curve and transmission electronic microscopy (TEM) were conducted in order to determine the effect of the plant extract on bacterial growth and ultrastructure.
View Article and Find Full Text PDFNew Phytol
November 1997
United States Department of Agriculture, Forest Service, Pacific Northwest Research Station, Forestry Sciences Laboratory, 3200 Jefferson Way, Corvallis, Oregon, 97331, USA.
Interspecific C transfer was studied in laboratory microcosms containing pairs of 6-month-old Betula papyrifera Marsh, and Pseudotsuga menziesii (Mirb.) Franca seedlings growing in individual, root-restrictive (28μm pore size) pouches filled with field soil. Interspecific transfer was examined by reciprocal labelling of seedlings with CO and CO .
View Article and Find Full Text PDFNew Phytol
November 1997
Department of Botany, University of Guelph. Guelph, Ontario, NIG 2W1, Canada.
Seedlings of Pseudotsuga menziesii (Mirb.) Franco, Pinus ponderosa Dougl. ex Laws, Arbutus menziesii Pursh.
View Article and Find Full Text PDFNew Phytol
August 1989
Department of Forest Science, Oregon State University, Corvallis, Oregon 97331 USAUSDA Forest Service, Pacific Northwest Research Station, Corvallis, Oregon 97331 USA.
To test the effect of ectomycorrhizal fungi (EMF) on interactions between host plants, Pseudotsuga menziesii (Mirb.) Franco and Pinus ponderosa Dougl. ex.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!