Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
J Proteome Res ; 9(11): 5715-26, 2010 Nov 05.
Artigo em Inglês | MEDLINE | ID: mdl-20831161

RESUMO

Legume pods serve important functions during seed development and are themselves sources of food and feed. Compared to seeds, the metabolism and development of pods are not well-defined. The present characterization of pods from the model legume Lotus japonicus, together with the detailed analyses of the pod and seed proteomes in five developmental stages, paves the way for comparative pathway analysis and provides new metabolic information. Proteins were analyzed by two-dimensional gel electrophoresis and tandem-mass spectrometry. These analyses lead to the identification of 604 pod proteins and 965 seed proteins, including 263 proteins distinguishing the pod. The complete data set is publicly available at http://www.cbs.dtu.dk/cgi-bin/lotus/db.cgi , where spots in a reference map are linked to experimental data, such as matched peptides, quantification values, and gene accessions. Identified pod proteins represented enzymes from 85 different metabolic pathways, including storage globulins and a late embryogenesis abundant protein. In contrast to seed maturation, pod maturation was associated with decreasing total protein content, especially proteins involved in protein biosynthesis and photosynthesis. Proteins detected only in pods included three enzymes participating in the urea cycle and four in nitrogen and amino group metabolism, highlighting the importance of nitrogen metabolism during pod development. Additionally, five legume seed proteins previously unassigned in the glutamate metabolism pathway were identified.


Assuntos
Frutas/química , Lotus/química , Proteínas de Plantas/análise , Proteoma/análise , Sementes/química , Fabaceae , Frutas/crescimento & desenvolvimento , Lotus/crescimento & desenvolvimento , Redes e Vias Metabólicas , Sementes/crescimento & desenvolvimento , Espectrometria de Massas em Tandem
2.
Appl Biochem Biotechnol ; 160(4): 1124-9, 2010 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-19444389

RESUMO

The formation of noncovalent complexes between glycosidase, endo-1,4-beta-D-mannanase, and ionic surfactant di(2-ethylhexyl) sodium sulfosuccinate (AOT) was shown to promote protein transfer into organic solvents such as xylene and hexane. It was found that mannanase can be solubilized in hexane and in xylene with concentration at least 2.5 and 2.0 mg/ml, respectively. The catalytic activity of the enzyme in hexane spontaneously increases with the concentration of AOT and is about 10% of the activity in aqueous system. In xylene, a catalytic activity higher than that in bulk aqueous conditions was found for the samples containing 0.1-0.3 mg/ml of mannanase, while for the samples with a higher concentration of enzyme, the activity was hardly detected.


Assuntos
Hexanos/química , Manosidases/isolamento & purificação , Xilenos/química , Fracionamento Químico/métodos , Manosidases/química , Manosidases/metabolismo , Solubilidade , Succinatos/química
3.
Plant Physiol ; 149(3): 1325-40, 2009 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19129418

RESUMO

We have characterized the development of seeds in the model legume Lotus japonicus. Like soybean (Glycine max) and pea (Pisum sativum), Lotus develops straight seed pods and each pod contains approximately 20 seeds that reach maturity within 40 days. Histological sections show the characteristic three developmental phases of legume seeds and the presence of embryo, endosperm, and seed coat in desiccated seeds. Furthermore, protein, oil, starch, phytic acid, and ash contents were determined, and this indicates that the composition of mature Lotus seed is more similar to soybean than to pea. In a first attempt to determine the seed proteome, both a two-dimensional polyacrylamide gel electrophoresis approach and a gel-based liquid chromatography-mass spectrometry approach were used. Globulins were analyzed by two-dimensional polyacrylamide gel electrophoresis, and five legumins, LLP1 to LLP5, and two convicilins, LCP1 and LCP2, were identified by matrix-assisted laser desorption ionization quadrupole/time-of-flight mass spectrometry. For two distinct developmental phases, seed filling and desiccation, a gel-based liquid chromatography-mass spectrometry approach was used, and 665 and 181 unique proteins corresponding to gene accession numbers were identified for the two phases, respectively. All of the proteome data, including the experimental data and mass spectrometry spectra peaks, were collected in a database that is available to the scientific community via a Web interface (http://www.cbs.dtu.dk/cgi-bin/lotus/db.cgi). This database establishes the basis for relating physiology, biochemistry, and regulation of seed development in Lotus. Together with a new Web interface (http://bioinfoserver.rsbs.anu.edu.au/utils/PathExpress4legumes/) collecting all protein identifications for Lotus, Medicago, and soybean seed proteomes, this database is a valuable resource for comparative seed proteomics and pathway analysis within and beyond the legume family.


Assuntos
Lotus/embriologia , Lotus/metabolismo , Modelos Biológicos , Proteoma/metabolismo , Sementes/crescimento & desenvolvimento , Sementes/metabolismo , Biomassa , Cromatografia Líquida , Bases de Dados de Proteínas , Eletroforese em Gel Bidimensional , Ácidos Graxos/análise , Globulinas/genética , Globulinas/metabolismo , Internet , Proteínas de Armazenamento de Sementes/metabolismo , Sementes/citologia , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz , Amido/metabolismo , Água
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA