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1.
Plant Cell Rep ; 39(5): 669-682, 2020 May.
Artigo em Inglês | MEDLINE | ID: mdl-32123995

RESUMO

KEY MESSAGE: SBTX has defensive role against C. kikuchii, and therefore, its constituent genes SBTX17 and SBTX27 are promising candidates to engineer pathogen resistant plants. Soybean (Glycine max [L.] Merr.) is economically the most important legume crop in the world. Its productivity is strongly affected by fungal diseases, which reduce soybean production and seed quality and cause losses of billions of dollars worldwide. SBTX is a protein that apparently takes part in the defensive chemical arsenal of soybean against pathogens. This current study provides data that reinforce this hypothesis. Indeed, SBTX inhibited in vitro the mycelial growth of Cercospora kikuchii, it is constitutively located in the epidermal region of the soybean seed cotyledons, and it is exuded from mature imbibed seeds. Moreover, RT-qPCR analysis of the SBTX associated genes, SBTX17 and SBTX27, which encode for the 17 and 27 kDa polypeptide chains, showed that both genes are expressed in all studied plant tissues during the soybean development, with the highest levels found in the mature seeds and unifoliate leaves. In addition, to assess a local response of the soybean secondary leaves from 35-day-old plants, they were inoculated with C. kikuchii and treated with salicylic acid. It was verified using RT-qPCR that SBTX17 and SBTX27 genes overexpressed in leaves compared to controls. These findings strongly suggest that SBTX has defensive roles against C. kikuchii. Therefore, SBTX17 and SBTX27 genes are promising candidates to engineer pathogen resistant plants.


Assuntos
Ascomicetos , Resistência à Doença/genética , Glycine max/metabolismo , Glicoproteínas/fisiologia , Doenças das Plantas/microbiologia , Ácido Salicílico/farmacologia , Proteínas de Soja/fisiologia , Ascomicetos/efeitos dos fármacos , Ascomicetos/crescimento & desenvolvimento , Cotilédone/genética , Cotilédone/metabolismo , Expressão Gênica , Regulação da Expressão Gênica de Plantas/efeitos dos fármacos , Regulação da Expressão Gênica de Plantas/genética , Glicoproteínas/genética , Glicoproteínas/metabolismo , Glicoproteínas/farmacologia , Folhas de Planta/efeitos dos fármacos , Folhas de Planta/genética , Folhas de Planta/metabolismo , Folhas de Planta/microbiologia , Regiões Promotoras Genéticas , Sementes/genética , Sementes/metabolismo , Proteínas de Soja/genética , Proteínas de Soja/metabolismo , Proteínas de Soja/farmacologia , Glycine max/genética , Glycine max/crescimento & desenvolvimento , Glycine max/microbiologia , Regulação para Cima
2.
J Agric Food Chem ; 63(22): 5335-43, 2015 Jun 10.
Artigo em Inglês | MEDLINE | ID: mdl-26034922

RESUMO

Several studies have described the effects of seed exudates against microorganisms, but only few of them have investigated the proteins that have defensive activity particularly against nematode parasites. This study focused on the proteins released in the exudates of soybean seeds and evaluated their nematicidal properties against Meloidogyne incognita. A proteomic approach indicated the existence of 63 exuded proteins, including ß-1,3-glucanase, chitinase, lectin, trypsin inhibitor, and lipoxygenase, all of which are related to plant defense. The presence of some of these proteins was confirmed by their in vitro activity. The soybean exudates were able to reduce the hatching of nematode eggs and to cause 100% mortality of second-stage juveniles (J2). The pretreatment of J2 with these exudates resulted in a 90% reduction of the gall number in tobacco plants. These findings suggest that the exuded proteins are directly involved in plant defense against soil pathogens, including nematodes, during seed germination.


Assuntos
Antinematódeos/química , Glycine max/química , Exsudatos de Plantas/química , Proteínas de Plantas/química , Proteoma/química , Sementes/química , Tylenchoidea/efeitos dos fármacos , Animais , Antinematódeos/metabolismo , Antinematódeos/farmacologia , Espectrometria de Massas , Exsudatos de Plantas/metabolismo , Exsudatos de Plantas/farmacologia , Proteínas de Plantas/metabolismo , Proteínas de Plantas/farmacologia , Proteoma/metabolismo , Proteoma/farmacologia , Sementes/metabolismo , Glycine max/metabolismo , Tylenchoidea/crescimento & desenvolvimento
3.
Front Microbiol ; 5: 5, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24523715

RESUMO

Jatropha curcas seed cake is a low-value by-product resulting from biodiesel production. The seed cake is highly toxic, but it has great potential for biotechnology applications as it is a repository of biomolecules that could be important in agriculture, medicine, and industry. To explore this potential, a novel trypsin inhibitor called JcTI-I was purified by fractionation of the crude extract with trichloroacetic acid (2.5%, v/v) followed by affinity chromatography (Trypsin-Sepharose 4B) and molecular exclusion (Sephacryl S-200). Non-reducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis and gel filtration showed that JcTI-I has approximately 20.0~kDa. Mass spectrometry analysis revealed that the intact molecular mass of JcTI-I is 10.252~kDa. Moreover, JcTI-I is a glycoprotein with 6.4% (m/m) carbohydrates, pI of 6.6, N-terminal sequence similarity around 60% to plant albumins and high stability to heat, pH, and salinity. JcTI-I presented antibacterial activity against the human pathogenic bacteria Salmonella enterica subspecies enterica serovar choleraesuis and Staphylococcus aureus, with minimum inhibitory concentration less than 5~µg/mL. Furthermore, JcTI-I did have inhibitory activity against the serine proteases from the tested bacteria. Otherwise, no hemolytic activity of human erythrocytes and signs of acute toxicity to mice were observed for JcTI-I. The results demonstrate the benefits of J. curcas seed cake as a source of trypsin inhibitor with potential for biotechnological application as a new antimicrobial agent against human pathogenic bacteria.

4.
PLoS One ; 8(7): e70425, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23894655

RESUMO

Soybean toxin (SBTX) is an antifungal protein from soybeans with broad inhibitory activity against the growth and filamentation of many fungi, including human and plant pathogenic species such as Candida albicans, Candida parapsilosis, Aspergillus niger, Penicillium herquei, Cercospora sojina and Cercospora kikuchii. Understanding the mechanism by which SBTX acts on fungi and yeasts may contribute to the design of novel antifungal drugs and/or the development of transgenic plants resistant to pathogens. To this end, the polymorphic yeast C. albicans was chosen as a model organism and changes in the gene expression profile of strain SC5314 upon exposure to SBTX were examined. Genes that were differentially regulated in the presence of SBTX were involved in glucose transport and starvation-associated stress responses as well as in the control of both the induction and repression of C. albicans hyphal formation. Transmission electron microscopy showed that C. albicans cells exposed to SBTX displayed severe signs of starvation and were heavily granulated. Our data were indicative of C. albicans cell starvation despite sufficient nutrient availability in the medium; therefore, it can be speculated that SBTX blocks nutrient uptake systems. Because neither the starvation signal nor the alkaline response pathway lead to the induction of hyphae, we hypothesise that conflicting signals are transmitted to the complex regulatory network controlling morphogenesis, eventually preventing the filamentation signal from reaching a significant threshold.


Assuntos
Aminoácidos/metabolismo , Candida albicans/efeitos dos fármacos , Candida albicans/crescimento & desenvolvimento , Metabolismo dos Carboidratos/efeitos dos fármacos , Glycine max/química , Proteínas de Plantas/farmacologia , Estresse Fisiológico/efeitos dos fármacos , Antifúngicos/farmacologia , Transporte Biológico/efeitos dos fármacos , Candida albicans/genética , Candida albicans/metabolismo , Deleção de Genes , Análise de Sequência com Séries de Oligonucleotídeos , Transcriptoma/efeitos dos fármacos
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