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1.
J Plant Physiol ; 263: 153465, 2021 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-34225176

RESUMEN

Tea is one of the most consumed beverages worldwide, and trichome formation in tea plant leaves impairs their commercial value. In Arabidopsis thaliana leaves, trichome formation is negatively regulated by the CPC family genes, which encode R3-type MYB transcription factors. Here, we identified six CPC-like genes in a tea plant (Camellia sinensis var. sinensis) for the first time. Simulated three-dimensional structure of the MYB domains of all the six CPC-like proteins exhibited negative charge on the surface, as observed on that of the Arabidopsis CPC protein that does not bind to DNA, indicating their similarity with regard to molecular interaction. We further found that the six CPC-like genes were differentially expressed in different developmental stages of tea leaves, and four out of the six genes were upregulated in the youngest 1st leaves, which formed more trichomes than other older leaves. Although it does not establish a causal link, the correlation between differential expression of CPC-like genes and variable trichome formation suggests that the R3-type MYB transcription factors are potential precipitating factors in affecting the value of tea leaf.


Asunto(s)
Camellia sinensis/genética , Camellia sinensis/fisiología , Genes de Plantas , Hojas de la Planta/genética , Hojas de la Planta/fisiología , Proteínas Proto-Oncogénicas c-myb/genética , Tricomas/genética , Tricomas/fisiología , Productos Agrícolas/genética , Productos Agrícolas/fisiología , Regulación de la Expresión Génica de las Plantas , Variación Genética , Japón , Proteínas Proto-Oncogénicas c-myb/fisiología
2.
Biosci Biotechnol Biochem ; 85(7): 1753-1758, 2021 Jun 24.
Artículo en Inglés | MEDLINE | ID: mdl-34036320

RESUMEN

An extract of date (fruit of a palm tree) residue plus food-grade glutamate, acetic acid, and yeast extract (date residue extract mix, DREM) has been successfully fermented with using Lactobacillus brevis JCM 1059T to produce gamma-aminobutyric acid (GABA). Here, mouse splenocytes were found to be viable when supplemented with DREM and fermented DREM containing GABA (fDREM). The addition of DREM and fDREM resulted in the secretion of tumor necrosis factor (TNF)-α from the splenocytes, fDREM being more effective than DREM. The TNF-α secretion with DREM was elevated by exogenous addition of GABA and that with fDREM was in part mediated via A-type GABA receptors. Contrary to general understanding of the suppressive effects of GABA on various biological functions, our findings suggest that GABA-containing fDREM arguments the immune function as a food and pharmaceutical material.


Asunto(s)
Cronología como Asunto , Fermentación , Phoeniceae/química , Extractos Vegetales/química , Bazo/citología , Ácido gamma-Aminobutírico/química , Animales , Femenino , Levilactobacillus brevis/metabolismo , Ratones , Ratones Endogámicos BALB C , Bazo/inmunología , Factor de Necrosis Tumoral alfa/metabolismo
3.
Biosci Biotechnol Biochem ; 84(5): 1069-1072, 2020 May.
Artículo en Inglés | MEDLINE | ID: mdl-31931681

RESUMEN

Gamma-aminobutyric acid (GABA) is produced by Lactobacillus brevis using date residue fermentation. In this study, the GABA production method was improved, for which L. brevis strain JCM 1059T was the most efficient among the four L. brevis strains examined. This was presumably due to a difference in the expression level of the gene encoding glutamate decarboxylase that catalyzes GABA synthesis.Abbreviation: GABA: gamma-aminobutyric acid.


Asunto(s)
Glutamato Descarboxilasa/genética , Levilactobacillus brevis/enzimología , Levilactobacillus brevis/genética , Phoeniceae/química , Extractos Vegetales/metabolismo , Ácido gamma-Aminobutírico/metabolismo , Secuencia de Aminoácidos , Proteínas Bacterianas/metabolismo , Fermentación , Regulación Bacteriana de la Expresión Génica , Genes Bacterianos/genética , Glutamato Descarboxilasa/metabolismo , Concentración de Iones de Hidrógeno , ARN Ribosómico 16S/genética , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
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