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1.
J Microbiol Biotechnol ; 34(5): 1-10, 2024 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-38563101

RESUMO

This study explores beneficial bacteria isolated from the roots and rhizosphere soil of Khao Rai Leum Pua Phetchabun rice plants. A total of 315 bacterial isolates (KK1 to KK315) were obtained. Plant growth-promoting traits (phosphate solubilization and indole-3-acetic acid (IAA) production), and antimicrobial activity against three rice pathogens (Curvularia lunata NUF001, Bipolaris oryzae 2464, and Xanthomonas oryzae pv. oryzae) were assessed. KK074 was the most prolific in IAA production, generating 362.6±28.0 µg/ml, and KK007 excelled in tricalcium phosphate solubilization, achieving 714.2±12.1 µg/ml. In antimicrobial assays using the dual culture method, KK024 and KK281 exhibited strong inhibitory activity against C. lunata, and KK269 was particularly effective against B. oryzae. In the evaluation of antimicrobial metabolite production, KK281 and KK288 exhibited strong antifungal activities in cell-free supernatants. Given the superior performance of KK281, taxonomically identified as Bacillus sp. KK281, it was investigated further. Lipopeptide extracts from KK281 had significant antimicrobial activity against C. lunata and a minimum inhibitory concentration (MIC) of 3.1 mg/ml against X. oryzae pv. oryzae. LC-ESI-MS/MS analysis revealed the presence of surfactin A in the lipopeptide extract. The crude extract was non-cytotoxic to the L-929 cell line at tested concentrations. In conclusion, the in vitro plant growth-promoting and disease-controlling attributes of Bacillus sp. KK281 make it a strong candidate for field evaluation to boost plant growth and manage disease in upland rice.

2.
Molecules ; 28(16)2023 Aug 08.
Artigo em Inglês | MEDLINE | ID: mdl-37630201

RESUMO

Actinobacteria produce a broad spectrum of bioactive substances that are used in the pharmaceutical, agricultural, and biotechnology industries. This study investigates the production of bioactive substances in Streptomyces, isolated from soil under five tropical plants, focusing on their potential as natural antibacterial dyes for silk fabrics. Out of 194 isolates, 44 produced pigments on broken rice as a solid substrate culture. Eight antibacterial pigmented isolates from under Magnolia baillonii (TBRC 15924, TBRC 15927, TBRC 15931), Magnolia rajaniana (TBRC 15925, TBRC 15926, TBRC 15928, TBRC 15930), and Cinnamomum parthenoxylon (TBRC 15929) were studied in more detail. TBRC 15927 was the only isolate where all the crude extracts inhibited the growth of the test organisms, Staphylococcus epidermidis TISTR 518 and S. aureus DMST 4745. The bioactive compounds present in TBRC 15927 were identified through LC-MS/MS analysis as belonging to the actinomycin group, actinomycin D (or X1), X2, and X0ß. Also, the ethyl acetate crude extract exhibited non-toxicity at an IC50 value of 0.029 ± 0.008 µg/mL on the mouse fibroblast L-929 assay. From the 16S rRNA gene sequence analysis, TBRC 15927 had 100% identity with Streptomyces gramineus JR-43T. Raw silk dyed with the positive antimicrobial TBRC 15927 extract (8.35 mg/mL) had significant (>99.99%) antibacterial properties. Streptomyces gramineus TBRC 15927 is the first actinomycin-producing strain reported to grow on broken rice and shows promise for antibacterial silk dyeing.


Assuntos
Solo , Streptomyces , Animais , Camundongos , Dactinomicina/farmacologia , Seda , Cromatografia Líquida , RNA Ribossômico 16S/genética , Staphylococcus aureus , Espectrometria de Massas em Tandem , Antibacterianos/farmacologia , Streptomyces/genética
3.
Biomolecules ; 10(12)2020 12 16.
Artigo em Inglês | MEDLINE | ID: mdl-33339185

RESUMO

Recent developments in chemotherapy focus on target-specific mechanisms, which occur only in cancer cells and minimize the effects on normal cells. DNA damage and repair pathways are a promising target in the treatment of cancer. In order to identify novel compounds targeting DNA repair pathways, two key proteins, 53BP1 and RAD54L, were tagged with fluorescent proteins as indicators for two major double strand break (DSB) repair pathways: non-homologous end-joining (NHEJ) and homologous recombination (HR). The engineered biosensor cells exhibited the same DNA repair properties as the wild type. The biosensor cells were further used to investigate the DNA repair activities of natural biological compounds. An extract from Phyllosticta sp., the endophyte isolated from the medicinal plant Garcinia cowa Roxb. ex Choisy, was tested. The results showed that the crude extract induced DSB, as demonstrated by the increase in the DNA DSB marker γH2AX. The damaged DNA appeared to be repaired through NHEJ, as the 53BP1 focus formation in the treated fraction was higher than in the control group. In conclusion, DNA repair-based biosensors are useful for the preliminary screening of crude extracts and biological compounds for the identification of potential targeted therapeutic drugs.


Assuntos
Técnicas Biossensoriais , Dano ao DNA , Reparo do DNA , Endófitos/química , Garcinia/microbiologia , Extratos Vegetais/farmacologia , Animais , Linhagem Celular , Sobrevivência Celular , Galinhas , Quebras de DNA de Cadeia Dupla , Reparo do DNA por Junção de Extremidades , DNA Helicases/metabolismo , Proteínas de Ligação a DNA/metabolismo , Fermentação , Fungos/metabolismo , Garcinia/metabolismo , Histonas/metabolismo , Recombinação Homóloga , Plantas Medicinais , Sementes/metabolismo , Proteína 1 de Ligação à Proteína Supressora de Tumor p53/metabolismo
4.
Chemistry ; 22(13): 4551-5, 2016 Mar 18.
Artigo em Inglês | MEDLINE | ID: mdl-26880363

RESUMO

Thailand possesses a rich diversity of orchid species that, in turn, live in symbiosis with a wide variety of fungi. Such endophytes have the potential to produce secondary metabolites with bioactivity against orchid and/or human pathogens. The orchid-associated fungal strain Daldinia eschscholtzii was found to produce a diverse range of aromatic polyketides including the new naphthalene derivatives daldionin, nodulones B and C, and daldinones F and G along with eight known compounds. Daldionin possesses an unprecedented oxane-linked binaphthyl ring system. These compounds demonstrate the high diversity of structural variations that are constructed during fungal biosynthesis, and the results include important observations concerning the biosynthesis of binaphthyl derivatives. Daldionin was found to have weak antiproliferative activity against HUVEC and K-562 cell lines. All but one of the isolated compounds showed moderate antimicrobial activity towards at least one of the four tested microbial strains.


Assuntos
Anti-Infecciosos/química , Anti-Infecciosos/farmacologia , Produtos Biológicos/química , Endófitos/química , Fungos/química , Compostos Heterocíclicos com 2 Anéis/química , Compostos Heterocíclicos com 2 Anéis/farmacologia , Compostos Heterocíclicos com 3 Anéis/química , Compostos Heterocíclicos com 3 Anéis/farmacologia , Naftalenos/química , Policetídeos/química , Produtos Biológicos/isolamento & purificação , Produtos Biológicos/metabolismo , Linhagem Celular , Endófitos/isolamento & purificação , Endófitos/metabolismo , Fungos/metabolismo , Humanos , Tailândia
5.
Nat Prod Commun ; 5(4): 567-70, 2010 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-20433074

RESUMO

A new stemphol derivative, stemphol 1-O-beta-D-galactopyranoside (1b), together with three known metabolites, stemphol (1a), indole-3-carboxylic acid, and kojic acid, has been isolated from the ethyl acetate extract of cultures of Gaeumannomyces amomi BCC4066, an endophytic fungus found on healthy parts of ginger (Alpinia malaccensis; Thai name Kha-pa). The structure of 1b was established via spectroscopic methods, including 2D NMR measurements and GC/MS experiments.


Assuntos
Ascomicetos/química , Galactosídeos/isolamento & purificação , Resorcinóis/isolamento & purificação , Galactosídeos/química , Ressonância Magnética Nuclear Biomolecular , Rotação Ocular , Resorcinóis/química , Espectrometria de Massas por Ionização por Electrospray
6.
Acta Crystallogr Sect E Struct Rep Online ; 65(Pt 6): o1366, 2009 May 23.
Artigo em Inglês | MEDLINE | ID: mdl-21583216

RESUMO

In the title compound, C(15)H(24)O(2), a natural dialkyl-resorcinol commonly named stemphol, the mol-ecules are linked into C(6) and C(2) (2)(4) chains and R(4) (4)(16) rings by inter-molecular O-H⋯O hydrogen bonds, creating mol-ecular sheets parallel to the (010) plane. The alkyl chains are directed orthogonally away from these planes in almost complete extension.

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