Expression of a Soybean Hydroxyproline-Rich Glycoprotein Gene Is Correlated with Maturation of Roots1

A novel extensin gene has been identified in soybean (Glycine max L.) that encodes a hydroxyproline-rich glycoprotein (SbHRGP3) with two different domains. In this study expression of SbHRGP3 was investigated during soybean root development. SbHRGP was expressed in roots of mature plants, as well as seedlings, and showed a distinct pattern of expression during root development. The expression of SbHRGP3 increased gradually during root development of seedlings and reached a maximum while the secondary roots were maturing. The maximum expression level was contributed mainly by the secondary roots rather than by the primary root. Furthermore, expression of SbHRGP3 was preferentially detected in the regions undergoing maturation of the primary and secondary roots. These results imply that the expression of SbHRGP3 is regulated in an organ- and development-specific manner and that in soybean SbHRGP3 expression may be required for root maturation, presumably for the cessation of root elongation. Wounding and sucrose in combination enhanced expression of SbHRGP3 in roots, whereas both wounding and sucrose were required for the expression of SbHRGP3 in leaves.

Identification of Inositol 1,3,4-Trisphosphate 5-Kinase and Inositol 1,3,4,5-Tetrakisphosphate 6-Kinase in Immature Soybean Seeds

In extracts of immature soybean (Glycine max [L.] Merr.) seeds inositol tetrakisphosphate was formed from [3H]inositol 1,3,4-trisphosphate but not from [3H]inositol 1,4,5-trisphosphate. Inositol 1,3,4-trisphosphate kinase was purified to a specific activity of 3.55 min−1 mg−1 by polyethylenimine clarification and anion-exchange chromatography. The partially purified enzyme converted [3H]inositol 1,3,4-trisphosphate to inositol 1,3,4,5-tetrakisphosphate as the major product and inositol 1,3,4,6- and/or 1,2,3,4-tetrakisphosphate as the minor product. Subsequent experiments revealed a separate inositol 1,3,4,5-tetrakisphosphate 6-kinase activity, which could link these enzymes to inositol hexakisphosphate synthesis via the previously reported inositol 1,3,4,5,6-pentakisphosphate 2-kinase. The apparent Km values for inositol 1,3,4-trisphosphate kinase were 200 ± 0 nm for inositol 1,3,4-trisphosphate and 171 ± 4 μm for ATP, and the reaction was not reversible. The kinetics were such that no activity could be detected using unlabeled inositol 1,3,4-trisphosphate and [γ-32P]ATP, which suggested that other kinases may have been observed when less purified fractions were incubated with radiolabeled ATP. Inositol 1,3,4-trisphosphate kinase was nonspecifically inhibited more than 80% by various inositol polyphosphates at a concentration of 100 μm.

Uridine 5′-Diphosphate-Glucose Dehydrogenase from Soybean Nodules

A highly purified preparation of uridine 5′-diphosphate (UDP)-glucose (Glc) dehydrogenase (DH; EC 1.1.1.22) has been characterized from soybean (Glycine max L.) nodules. The enzyme had native and subunit molecular masses of approximately 272 and 50 kD, respectively. UDP-Glc DH displayed typical hyperbolic substrate kinetics and had Km values for UDP-Glc and NAD+ of 0.05 and 0.12 mm, respectively. Thymidine 5′-diphosphate-Glc and UDP-galactose could replace UDP-Glc as the sugar nucleotide substrate to some extent, but the enzyme had no activity with NADP+. Soybean nodule UDP-Glc DH was labile in the absence of NAD+ and was inhibited by a heat-stable, low-molecular-mass solute in crude extracts of soybean nodules. UDP-Glc DH was also isolated from developing soybean seeds and shoots of 5-d-old wheat and canola seedlings and was shown to have similar affinities for UDP-Glc and NAD+ as those of the soybean nodule enzyme. UDP-Glc DH from all of these sources was most active in young, rapidly growing tissues.

Resistance gene analogs are conserved and clustered in soybean.

Sequences of cloned resistance genes from a wide range of plant taxa reveal significant similarities in sequence homology and structural motifs. This is observed among genes conferring resistance to viral, bacterial, and fungal pathogens. In this study, oligonucleotide primers designed for conserved sequences from coding regions of disease resistance genes N (tobacco), RPS2 (Arabidopsis) and L6 (flax) were used to amplify related sequences from soybean [Glycine max (L.) Merr.]. Sequencing of amplification products indicated that at least nine classes of resistance gene analogs (RGAs) were detected. Genetic mapping of members of these classes located them to eight different linkage groups. Several RGA loci mapped near known resistance genes. A bacterial artificial chromosome library of soybean DNA was screened using primers and probes specific for eight RGA classes and clones were identified containing sequences unique to seven classes. Individual bacterial artificial chromosomes contained 2-10 members of single RGA classes. Clustering and sequence similarity of members of RGA classes suggests a common process in their evolution. Our data indicate that it may be possible to use sequence homologies from conserved motifs of cloned resistance genes to identify candidate resistance loci from widely diverse plant taxa.

Lack of mycorrhizal autoregulation and phytohormonal changes in the supernodulating soybean mutant nts1007

Autoregulatory mechanisms have been reported in the rhizobial and the mycorrhizal symbiosis. Autoregulation means that already existing nodules or an existing root colonization by an arbuscular mycorrhizal fungus systemically suppress subsequent nodule formation/root colonization in other parts of the root system. Mutants of some legumes lost their ability to autoregulate the nodule number and thus display a supernodulating phenotype. On studying the effect of pre-inoculation of one side of a split-root system with an arbuscular mycorrhizal fungus on subsequent mycorrhization in the second side of the split-root system of a wild-type soybean (Glycine max L.) cv. Bragg and its supernodulating mutant nts1007, we observed a clear suppressional effect in the wild-type, whereas further root colonization in the split-root system of the mutant nts1007 was not suppressed. These data strongly indicate that the mechanisms involved in supernodulation also affect mycorrhization and support the hypothesis that the autoregulation in the rhizobial and the mycorrhizal symbiosis is controlled in a similar manner. The accumulation patterns of the plant hormones IAA, ABA and Jasmonic acid (JA) in non-inoculated control plants and split-root systems of inoculated plants with one mycorrhizal side of the split-root system and one non-mycorrhizal side, indicate an involvement of IAA in the autoregulation of mycorrhization. Mycorrhizal colonization of soybeans also resulted in a strong induction of ABA and JA levels, but on the basis of our data the role of these two phytohormones in mycorrhizal autoregulation is questionable.

Analyses of the community compositions of root rot pathogenic fungi in the soybean rhizosphere soil

Soybean ( Glycine max [L.] Merr.) root rot is an important disease of soybean under continuous cropping, and root rot is widely distributed throughout the world. This disease is extremely harmful, and it is difficult to prevent and control. The study aimed to elucidate the composition of root rot pathogenic fungal communities in the continuous cropping of soybean. In this study, we employed PCRDGGE technology to analyze the communities of root rot pathogenic fungi in soybean rhizosphere soil subjected to continuous cropping during a season with a high incidence of root rot in Heilongjiang province, China, the main soybean producing area in China. The results of 13 DGGE bands were analyzed by phylogenetic revealed that the predominant root rot pathogenic fungi in rhizosphere soil in the test area were Pythium ultimum and Fusarium species. The results of cluster analysis showed that the duration of continuous cropping, the soybean variety and the plant growth stage all had significant effects on the diversity of root rot pathogenic fungi in rhizosphere soil.

Teor de fenólicos totais e crescimento radicular em soja (Glycine max (L.) Merr.) inoculada com as bactérias endofítica e epifítica e sua exposição à ferrugem.

Os compostos fenólicos são formados no metabolismo secundário dos vegetais e estão envolvidos no mecanismo de defesa. O objetivo do trabalho foi avaliar o efeito dos isolados 0G e EN78 na produção de fenólicos totais na soja, frente à exposição à ferrugem da soja (Phakospora pachyrhizi), e no crescimento radicular. O isolado EN78 induziu um aumento no teor de fenólicos totais quando exposto à ferrugem, mesmo antes da manifestação do sintoma. Esse mesmo isolado apresentou eficiência simbiótica com o Biorhizo 10 (Bradyrhizobium elkanii e japonicum), promovendo o desenvolvimento radicular, enquanto que o isolado 0G não influiu no teor de fenólicos totais, mas induziu aumento da biomassa radicular.

Validación de la prueba de tetrazolio como método de vigor para semillas de Glycine max.

El objetivo de este estudio fue demostrar que la Prue- ba de Tetrazolio es un Método de Vigor para Glycine max, repetible dentro de los laboratorios y reproducible entre ellos. Se analizaron tres lotes de semillas de Glycine max, con una germinación de maior ou igual a 80% (lote 1: 92%; lote 2: 89% y lote 3: 80%), empleando la Prueba de Tetrazolio. En la validación participaron 6 laboratorios. Las semillas fueron clasificadas en cuatro categorías: vigor alto, vigor medio, vigor bajo y otras tinciones (semillas viables no vigoro- sas + semillas no viables). La suma de la proporción de las categorías de semillas de vigor alto, medio y bajo se expresó como Vigor-TZ (%). Los valores de Vigor-TZ (%) se encontraron dentro de los niveles de tolerancia esta- blecidos por ISTA. El dato de Vigor-TZ fue analizado sepa- radamente, usando el cálculo del valor z-scores, valores h y valores k. El cálculo de los valores z-scores reveló que los datos de Vigor-TZ no excedieron el valor 2, por lo tanto los resultados son considerados satisfactorios. Los valores h mostraron que cinco laboratorios no sobreesti- maron ni subestimaron los resultados de todos los lotes de semillas. Los valores k mostraron la variabilidad entre las repeticiones de cada uno de los lotes dentro de cada laboratorio. Las repeticiones estuvieron en tolerancia para todos los lotes y todos los laboratorios. La prueba fue re- petible dentro de los laboratorios y reproducible en diferen- tes laboratorios. Concluimos que el dato para Vigor-TZ (%) muestra una variación aceptable y, por lo tanto, la Prueba de Tetrazolio puede ser aplicada como un método de vigor para soja.

Avaliação do glifosato na interação entre Phakopsora pachyrhizi e Glycine max por meio do ácido Chiquímico. II: efeito curativo.

2009

Avaliação do glifosato na interação entre Phakopsora pachyrhizi e Glycine max por meio do ácido Chiquímico. I: efeito preventivo

2009

Contents and bioconversion of B-glycoside isoflavones to aglycones in the processing conditions of soybean tempeh.

The objective of this work was to evaluate the effect of the processing conditions of soybean tempeh on the contents of ??glycoside isoflavones and on their bioconversion into aglycones. Different times of soaking (6, 12, and 18 hours), cooking (15, 30, and 45 minutes), and fermentation (18, 24, and 30 hours) with Rhizopus oligosporus at 37°C were evaluated for tempeh preparation. Grains from the cultivar 'BRS 267' were used, and the experiment was carried out according to a central composite design (23). The response functions comprised the contents of genistin, malonyldaidzin, malonylgenistin, daidzein, and genistein, quantified by ultraperformance liquid chromatography (UPLC). Soaking, cooking, and fermentation times change the content, profile, and distribution of the different forms of isoflavones in tempeh. The highest bioconversion of glycoside isoflavones into aglycones occurred in 6?hour soaked soybean grains, whose cotyledons were cooked for 15 minutes and subjected to 18?hour fermentation. RESUMO:O objetivo deste trabalho foi avaliar o efeito das condições de processamento do tempeh de soja sobre o conteúdo de isoflavonas ??glicosídeos e sobre sua bioconversão em agliconas. Diferentes tempos de maceração (6, 12 e 18 horas), cozimento (15, 30 e 45 minutos) e fermentação (18, 24 e 30 horas) com Rhizopus oligosporus a 37°C foram avaliados na preparação do tempeh. Foram utilizados grãos da cultivar 'BRS 267', e o experimento foi realizado de acordo com um delineamento composto central (23). As funções?respostas compreenderam o teor de genistina, malonildaidzina, malonilgenistina, daidzeína e genisteína, quantificadas por cromatografia líquida de ultraeficiência (CLUE). Os tempos de maceração, cozimento e fermentação alteraram o conteúdo, o perfil e a distribuição das diferentes formas de isoflavonas no tempeh. A maior bioconversão de ??glicosídeos em agliconas ocorreu em grãos de soja macerados por 6 horas, cujos cotilédones foram cozidos por 15 minutos e submetidos à fermentação por 18 horas.

Decomposição e liberação de nutrientes de resíduos culturais em áreas de plantio de soja (Glycine max) sob plantio direto no Cerrado Goiano.

A avaliação da decomposição dos resíduos vegetais adicionados ao solo pelas plantas de cobertura permite uma melhor compreensão do fornecimento de nutrientes para as culturas de interesse comercial. O objetivo do trabalho foi avaliar a taxas de decomposição e a dinâmica da liberação de N de resíduos culturais na entre safra da Soja sob plantio direto. Os resíduos utilizados foram a braquiária (Brachiaria sp.) e sorgo (Sorghum bicolor L. Moench). A produção média de biomassa de braquiária foi de 6,1 Mg ha-1 e de 3,8 Mg ha-1 no tratamento com sorgo. A decomposição da matéria seca e a liberação de nutrientes foram monitoradas por meio de coletas dos resíduos contidos em sacolas de decomposição, realizadas 15, 30, 60, 90, 120 dias após a adição das sacolas de decomposição nas áreas de estudo. Os T1/2 da massa seca remanescente diferiram estatisticamente entre os sistemas avaliados. A braquiária apresentou menores valores de meia vida quando comparados ao sorgo. Este comportamento pode ser atribuído provavelmente, às grandes quantidades de biomassa acumulada pela braquiária, favorecendo maiores teores de umidade no solo, e uma menor relação C/N da braquiária quando comparada ao sorgo.

Avaliação do uso do número de folhas de plantas de soja (Glycine max) para o monitoramento da interferência de plantas daninhas na cultura.

No ano agrícola 1990/91, em Jaguariúna, Estado de São Paulo, Brasil, foi realizado um experimento com o objetivo de avaliar o uso do numero de folhas trifolioladas da soja para o monitoramento da interferência das plantas daninhas, dando subsídios para a definição de parâmetros para o processo de tomada de decisão de controle. Foi usado o delineamento no campo em blocos casualizados, onde os tratamentos consistiram de diferentes épocas de controle através da capina, e uma testemunha sem capina e outra capinada durante todo o ciclo da cultura. As plantas daninhas predominantes na área do experimento foram: Brachiaria plantaginea e Sida gleziovii. Os dados de produtividade da cultura ajustaram-se ao modelo polinomial quadrático, através do qual determinou-se que a melhor época de controle foi aos 43 dias após a emergência da soja. A diferença entre o numero de folha de plantas de soja convivendo com a comunidade de plantas daninhas na produtividade da cultura, apostando diferença significativa aos 35 dias.