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1.
Chem Biodivers ; 21(6): e202400619, 2024 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-38680104

RESUMO

Salvia lanigera Poir. is a small herbaceous perennial species with violet flowers that grows in low-altitude deserts, and sandy loam. During the collection of S. lanigera, unusual populations with white flowers were found. Therefore, the two populations (violet- and white-flowered) were subjected to comparative investigations, including DNA fingerprinting, chemical composition, and biological evaluation. The two populations showed DNA variations, with 6.66 % polymorphism in ISSR and 25 % in SCoT markers. GC/MS and UHPLC/HRMS of aqueous methanol extracts, led to the tentative identification of 43 and 50 compounds in both populations. In addition, the structures of nine compounds, including four first-time reported compounds in the species, were confirmed by NMR. Furthermore, the total extracts exhibited weak radical scavenging activity against DPPH and a lower inhibitory effect towards acetylcholinesterase. In conclusion, the obtained data suggested that the white-colored flower could be an additional important character record for the Egyptian S. lanigera.


Assuntos
Impressões Digitais de DNA , Flores , Metabolômica , Salvia , Salvia/química , Salvia/metabolismo , Egito , Flores/química , Flores/metabolismo , Extratos Vegetais/química , Extratos Vegetais/isolamento & purificação , Extratos Vegetais/farmacologia , Compostos de Bifenilo/antagonistas & inibidores , Cromatografia Gasosa-Espectrometria de Massas , Picratos/antagonistas & inibidores , Acetilcolinesterase/metabolismo , Inibidores da Colinesterase/farmacologia , Inibidores da Colinesterase/química , Inibidores da Colinesterase/isolamento & purificação , Inibidores da Colinesterase/metabolismo , Cromatografia Líquida de Alta Pressão
2.
Methods Mol Biol ; 1638: 125-142, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28755220

RESUMO

Molecular marker technologies which rely on DNA analysis provide powerful tools to assess biodiversity at different levels, i.e., among and within species. A range of different molecular marker techniques have been developed and extensively applied for detecting variability in date palm at the DNA level. Recently, the employment of gene-targeting molecular marker approaches to study biodiversity and genetic variations in many plant species has increased the attention of researchers interested in date palm to carry out phylogenetic studies using these novel marker systems. Molecular markers are good indicators of genetic distances among accessions, because DNA-based markers are neutral in the face of selection. Here we describe the employment of multidisciplinary molecular marker approaches: amplified fragment length polymorphism (AFLP), start codon targeted (SCoT) polymorphism, conserved DNA-derived polymorphism (CDDP), intron-targeted amplified polymorphism (ITAP), simple sequence repeats (SSR), and random amplified polymorphic DNA (RAPD) to assess genetic diversity in date palm.


Assuntos
Marcadores Genéticos/genética , Variação Genética/genética , Phoeniceae/genética , Análise do Polimorfismo de Comprimento de Fragmentos Amplificados/métodos , DNA de Plantas/genética , Repetições de Microssatélites/genética , Filogenia , Polimorfismo Genético/genética , Técnica de Amplificação ao Acaso de DNA Polimórfico/métodos
3.
Methods Mol Biol ; 1638: 227-244, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28755227

RESUMO

Molecular markers are used efficiently in the development and identification of gender-specific PCR-based markers in date palm. There is mounting evidence that different marker systems vary in their mechanisms of detecting polymorphism and genome coverage. Therefore, they could complement each other to generate accurate sex-specific markers in date palm. This chapter describes the uses of PCR-based molecular markers to develop and identify the gender in different date palm genotypes; these are amplified fragment length polymorphism (AFLP), start codon targeted polymorphism (SCoT), conserved DNA-derived polymorphism (CDDP), intron-targeted amplified polymorphism (ITAP), and random amplified polymorphic DNA (RAPD). Also described is how to characterize the identified markers by Sanger sequencing and to explore their functions through alignment of their sequences with the Genbank databases.


Assuntos
Marcadores Genéticos/genética , Phoeniceae/genética , Análise do Polimorfismo de Comprimento de Fragmentos Amplificados/métodos , Genótipo , Reação em Cadeia da Polimerase/métodos , Polimorfismo Genético/genética , Polimorfismo de Fragmento de Restrição/genética , Técnica de Amplificação ao Acaso de DNA Polimórfico/métodos
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