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1.
Microb Cell Fact ; 21(1): 261, 2022 Dec 16.
Article in English | MEDLINE | ID: mdl-36527127

ABSTRACT

BACKGROUND: Antarctica has one of the most extreme environments in the world. This region is inhabited by specifically adapted microorganisms that produce various unique secondary metabolites (e.g. pigments) enabling their survival under the harsh environmental conditions. It was already shown that these natural, biologically active molecules may find application in various fields of biotechnology. RESULTS: In this study, a cold-active brown-pigment-producing Pseudomonas sp. ANT_H4 strain was characterized. In-depth genomic analysis combined with the application of a fosmid expression system revealed two different pathways of melanin-like compounds biosynthesis by the ANT_H4 strain. The chromatographic behavior and Fourier-transform infrared spectroscopic analyses allowed for the identification of the extracted melanin-like compound as a pyomelanin. Furthermore, optimization of the production and thorough functional analyses of the pyomelanin were performed to test its usability in biotechnology. It was confirmed that ANT_H4-derived pyomelanin increases the sun protection factor, enables scavenging of free radicals, and interacts with the iron from minerals. Moreover, it was shown for the first time that pyomelanin exhibits priming properties toward Calendula officinalis hairy roots in in vitro cultures. CONCLUSIONS: Results of the study indicate the significant biotechnological potential of ANT_H4-derived pyomelanin and open opportunities for future applications. Taking into account protective features of analyzed pyomelanin it may be potentially used in medical biotechnology and cosmetology. Especially interesting was showing that pyomelanin exhibits priming properties toward hairy roots, which creates a perspective for its usage for the development of novel and sustainable agrotechnical solutions.


Subject(s)
Melanins , Pseudomonas , Antarctic Regions , Pseudomonas/genetics , Pseudomonas/metabolism , Iron , Plant Roots , Free Radicals/metabolism , Minerals/metabolism
2.
Nat Prod Res ; 20(13): 1231-6, 2006 Nov.
Article in English | MEDLINE | ID: mdl-17127514

ABSTRACT

A new flavonol glycoside, kaempferol 3-O-alpha-L-arabinopyranosyl-7-O-beta-D-glucopyranoside (1), has been isolated from methanol extract of leaves of Datura suaveolens (Solanaceae), along with six other known compounds, which include kaempferol 3-O-alpha-L-arabinopyranoside (2), 3-phenyl lactic acid, 3-(3-indolyl) lactic acid, and its methyl ester, physalindicanol A and physalindicanol B. The structural elucidation of 1 and characterization of the known compounds are based on detailed spectral analysis (ESI-FTICR-MS and 2D-NMR). This is the first report of isolation of these compounds from this plant.


Subject(s)
Datura/chemistry , Glycosides/isolation & purification , Kaempferols/isolation & purification , Plant Extracts/isolation & purification , Glycosides/chemistry , Kaempferols/chemistry , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Optical Rotation , Plant Extracts/chemistry , Plant Leaves/chemistry , Spectrometry, Mass, Electrospray Ionization , Spectrophotometry, Infrared , Spectrophotometry, Ultraviolet
3.
Chem Pharm Bull (Tokyo) ; 54(4): 538-41, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16595960

ABSTRACT

Hyosgerin, a new optically active coumarinolignan, has been isolated and characterized along with three other coumarinolignans, venkatasin, cleomiscosin A and cleomiscosin B, from the seeds of Hyoscyamus niger L. The structure was determined on the basis of spectroscopic analysis and chemical conversion. The optical properties and absolute stereochemistry of these coumarinolignans have also been studied and discussed.


Subject(s)
Coumarins/pharmacology , Hyoscyamus/chemistry , Lignans/pharmacology , Plants, Medicinal , Seeds/chemistry , Coumarins/chemistry , Coumarins/isolation & purification , Dioxanes/chemistry , Dioxanes/isolation & purification , Dioxanes/pharmacology , Lignans/chemistry , Lignans/isolation & purification , Molecular Structure , Optical Rotation , Spectrum Analysis , Stereoisomerism
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