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1.
Polymers (Basel) ; 14(21)2022 Oct 31.
Artigo em Inglês | MEDLINE | ID: mdl-36365625

RESUMO

PTFE/Al reactive material is an energetic material that releases energy under impact conditions, resulting in a wide range of application prospects. In order to improve its damage ability-considering the higher heat of the reaction per unit mass when Ni2O3 is involved in the aluminothermic reaction-we designed and studied PTFE/Al/Ni2O3, a reaction material based on polytetrafluoroethylene (PTFE). We also designed two other kinds (PTFE/Al, PTFE/Al/CuO) for comparative study, with the mass fraction of the metal oxides added at 10%, 20%, and 30%, respectively. The quasi-static compression properties and impact initiation behavior of the material were investigated by a universal material testing machine and a drop hammer test. The reaction process of different materials under a high strain rate was recorded using a high-speed camera. The results show that with the increase in Ni2O3 content, the strength of the PTFE/Al/Ni2O3 reactive material shows an increasing trend followed by a decreasing trend. Among the three reactive materials, when the content of Al/Ni2O3 reaches 30 wt.%, the reaction duration is the longest (at 4 ms) and the reaction fireball is the largest. The addition of Ni2O3 is helpful to improve the reactivity and reaction duration of the PTEF/Al reactive material.

2.
PLoS One ; 4(9): e7209, 2009 Sep 30.
Artigo em Inglês | MEDLINE | ID: mdl-19789627

RESUMO

BACKGROUND: Soybean [Glycine max (L.) Merr.] is one of the most important crops for oil and protein resource. Improvement of stress tolerance will be beneficial for soybean seed production. PRINCIPAL FINDINGS: Six GmPHD genes encoding Alfin1-type PHD finger protein were identified and their expressions differentially responded to drought, salt, cold and ABA treatments. The six GmPHDs were nuclear proteins and showed ability to bind the cis-element "GTGGAG". The N-terminal domain of GmPHD played a major role in DNA binding. Using a protoplast assay system, we find that GmPHD1 to GmPHD5 had transcriptional suppression activity whereas GmPHD6 did not have. In yeast assay, the GmPHD6 can form homodimer and heterodimer with the other GmPHDs except GmPHD2. The N-terminal plus the variable regions but not the PHD-finger is required for the dimerization. Transgenic Arabidopsis plants overexpressing the GmPHD2 showed salt tolerance when compared with the wild type plants. This tolerance was likely achieved by diminishing the oxidative stress through regulation of downstream genes. SIGNIFICANCE: These results provide important clues for soybean stress tolerance through manipulation of PHD-type transcription regulator.


Assuntos
Arabidopsis/genética , Regulação da Expressão Gênica de Plantas , Glycine max/genética , Proteínas de Soja/genética , Fatores de Transcrição/genética , Sequência de Aminoácidos , Clonagem Molecular , Dimerização , Perfilação da Expressão Gênica , Dados de Sequência Molecular , Plantas Geneticamente Modificadas , Ligação Proteica , Estrutura Terciária de Proteína , Protoplastos/metabolismo , Homologia de Sequência de Aminoácidos , Estresse Fisiológico
3.
Theor Appl Genet ; 108(5): 842-50, 2004 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-14618239

RESUMO

A full-length gene GmSAMDC1, encoding the S-adenosylmethionine decarboxylase (SAMDC), a key enzyme involved in polyamine biosynthesis, was identified from soybean expressed sequence tags and was characterized. GmSAMDC1 encoded a peptide of 355 amino acids. When compared with other plant SAMDCs, the GmSAMDC1 protein had several highly conserved regions including a putative pro-enzyme cleavage site and a PEST sequence. The 5' leader sequence of the the GmSAMDC1 mRNA contained two additional open reading frames (ORFs), which may regulate the translational process. The genomic sequence of the GmSAMDC1 gene contained three introns in the 5' leader sequence, but no intron in the 3'-UTR or the main pro-enzyme ORF. A simple sequence repeat (SSR) was found in intron 2, and the GmSAMDC1 gene was mapped to linkage group D1 using this SSR. The genomic organization of the GmSAMDC1 gene in the subgenus Glycine and the subgenus Soja was found to be different by Southern-blot and PCR analysis. A pseudogene, GmSAMDC2, was also identified. This gene contained no intron and lost its two uORFs. Northern-blot analysis showed that the GmSAMDC1 gene expression was induced by salt, drought and cold, but not induced by wounding; suggesting that the gene was implicated in response to multiple-stress conditions.


Assuntos
Adenosilmetionina Descarboxilase/genética , Genoma de Planta , Glycine max/genética , Regiões 3' não Traduzidas , Adenosilmetionina Descarboxilase/química , Sequência de Aminoácidos , Sequência de Bases , Northern Blotting , Southern Blotting , Primers do DNA , DNA Complementar , Genes de Plantas , Íntrons , Dados de Sequência Molecular , Fases de Leitura Aberta , Reação em Cadeia da Polimerase , Pseudogenes , RNA Mensageiro/genética , Homologia de Sequência de Aminoácidos , Homologia de Sequência do Ácido Nucleico
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