Isolation of peroxidase from bean and millet compared with that from peanut

1994 ◽  
Vol 72 (10) ◽  
pp. 1432-1435 ◽  
Author(s):  
R. B. van Huystee ◽  
M. Malko ◽  
K. Wen ◽  
M. Gijzen

Purification of peanut (Arachis hypogaea L.) peroxidase in milligram amounts is feasible through its isolation from spent medium of cultured cells. Using the same and modified approaches for another cultured dicot and a monocot yielded only low amounts of peroxidase for bean (Phaseolus vulgaris) and millet (Setaria italica Beav.). We showed that the procedures used for millet rendered a purer fraction than the commercial crude fraction available for horseradish. The data suggest that cultured peanut cells in suspension culture are an ideal system for isolation of peroxidase in terms of the ease of purification and yield. Key words: peanut, bean, millet, peroxidase, purification, tissue.

2020 ◽  
Vol 55 (3) ◽  
pp. 189-196
Author(s):  
AH Erhenhi

Effects of drought and flooding on bean (Phaseolus vulgaris L.) and groundnut (Arachis hypogaea L.) were carried out and compared. Plant growth parameters, biomass content, chlorophyll, ash and soil metal content were studied. The result showed that bean was 21.3cm, 21.8cm and 21.1cm for control, drought and flooding while groundnut recorded 19.9cm, 102.3cm and 18.6cm for control, drought and flooding respectively. Biomass composition recorded little or no variation in fresh weight of stem in bean while groundnut varies from 4.77g – 5.05g accordingly. Leaf recorded highest value of fresh weight to be 6.44g recorded in bean cultivated in drought soil with the least recorded to be 3.61 in the control and flooded soil for groundnut plant. The result of the study showed that drought and flooding had relatively positive effects on the growth properties of bean and groundnut as both plants were able to germinate and grow under both conditions. Bangladesh J. Sci. Ind. Res.55(3), 189-196, 2020


2013 ◽  
Vol 1 (1) ◽  
pp. 45
Author(s):  
Yudiwanti Wahyu ◽  
Dede Rosyana Budiman

<p style="text-align: justify;">This research was aimed to evaluate the yield of 16 peanut leafspot resistant lines derived from cross between Gajah variety and GPNC-WS 4 line with four check varieties of peanut. The four check varieties of peanut consist of Gajah, Jerapah, Zebra Putih, and Sima. The experiment was carried out at Ciranjang District, Cianjur Regency, West Java, from February to May 2011. This research was arranged in randomized complete block design with three replications. Result showed that GWS 39 D, GWS 110 D, GWS 18 A1, GWS 79 A, and GWS 110 A2 were identified as lines with high yield. GWS 74 D, GWS 39 B, GWS 79 A, GWS 73 D, GWS 18 A1, GWS 134 A1, and GWS 110 A1 were identified as lines with high resistant level to leafspot of peanut. Two of sixteen lines had high yield and high resistant level to leafspot, they were GWS 79 A and GWS 18 A1.</p><p>Key words : peanut, yield evaluation, leaf spot resistant</p>


Plant Disease ◽  
2021 ◽  
Author(s):  
Saira Martínez-Salgado ◽  
Omar Romero-Arenas ◽  
Luis A. Morales-Mora ◽  
Alfonso Luna-Cruz ◽  
José A. Rivera-Tapia ◽  
...  

Peanut (Arachis hypogaea L.) is the third most important oilseed crop in the world. The cultivated area in Mexico is currently 52,046 ha with a production of 91,109 ton in 2018 (FAO, 2020). Puebla state ranks third in the national production with 9,313 ton (SIAP, 2020). In September 2019, typical symptoms of charcoal rot (Macrophomina phaseolina (Tassi) Goid.) were observed in about 50% of cultivar Virginia Champs peanuts, and it affecting 1.5 ha located in Chietla (18° 27' 39" N; 98° 37' 11" W), Puebla, Mexico. Diseased plants showed brown discoloration in stem and root rot, with chlorotic foliage, dark microsclerotia were observed on the stem and premature dying. To isolate the causal agent of these symptoms, 20 infected plants were recovered and processed in the laboratory. Ten pieces of stem and root tissue were selected from each plant, cut into small pieces 5-mm in length, superficially disinfested with 1% sodium hypochlorite for 3 min, followed by three rinses with sterile distilled water. Later, dried on sterile paper and placed on Petri plates containing potato dextrose agar (PDA) medium, which were kept at 28°C for 7 days (12 h light and 12 h dark). Four colonies were purified via hyphal tip culture, fungus was consistently isolated from the analyzed tissues; additional microcultures were prepared to observe phenotypic characteristics. Colonies showed dense growth, with a gray initial mycelium, becoming black after 7 days. Microesclerotia with spherical to oblong in shape were observed after 5 days on PDA, with a black coloration, measuring an average of 74 µm width × 110 µm length (n=40). Phylogenetic analysis was conducted by amplification and sequencing of the internal transcribed spacer (ITS) region with the ITS5 and ITS4 primers (White et al. 1990). The obtained sequences were deposited in GenBank database under accession numbers: MW585378, MW585379, MW585380, and MW585381 containing approximately 601 bp of the ITS1-5.8S-ITS2 region (complete sequence); they were 99% identical with the reference sequence of Macrophomina phaseolina (GenBank accession KF951698) isolated in Phaseolus vulgaris from Mexico. Based on the symptoms in the field, colony morphology, color, and shape of the microsclerotia, and molecular identification, the fungus was identified as M. phaseolina (Tassi) Goid. The pathogenicity test was performed on peanut plants cultivar Virginia Champs grown on plastic pots with an autoclaved peat/soil mixture under greenhouse conditions (70% relative humidity and 28°C). Fifty two-month-old peanut plants were inoculated using the toothpick method. The toothpicks were previously sterilized and then placed in Petri plates with each of the four colonies of M. phaseolina until colonization. Small wounds were made with those toothpicks in the roots, and a sterile toothpick was used in the control plants, the assays were performed twice. After three weeks, the inoculated plants exhibited symptoms of wilting chlorosis on the leaves and brown to dark brown discoloration of the vascular ring, while control plants remained healthy. M. phaseolina was re-isolated from symptomatic root tissues and identified by phylogenetic approach, fulfilling Koch’s postulates. To date, this fungus affects at least 372 hosts globally causing yield losses. Although in Mexico this fungus has been documented in Glycine max, Ipomoea batatas, Phaseolus vulgaris, Physalis ixocarpa, Saccharum officinarum, Sesamum indicum, Solanum melongena, S. tuberosum, and Sorghum bicolor (Farr and Rossman 2021). However, there are no reports of M. phaseolina as a potential pathogen on peanut; therefore, according to our knowledge, this is the first report of this fungus affecting A. hypogaea in Mexico.


2017 ◽  
Author(s):  
Marcelo Tacán ◽  
César Tapia ◽  
César Pérez

The effects of artificial aging and cryopreservation methods on the germination of seeds and embryonic axes of Phaseolus vulgaris and Arachis hypogaea , were studied. Aging and cryopreservation treatments in bean seeds not affect the germination percentage, reaching values not significantly different from control. Germination percentage was higher when isolated embryonic axes were studied. Aging treatments gave rise to larger bean seedlings than the controls and cryopreservation treatments affected the size depending on the explant used. In groundnut seeds, aging treatments and cryopreservation positively affected germination and vigor of seedlings, but embryonic axes from not rehydrated aging seeds not germinate. Undried groundnut seeds not survive cryopreservation, while the dried ones showed a germination behavior superior to the control. Embryonic axes tolerate immersion in liquid nitrogen but when droplet-vitrification was used, formed callus instead of seedlings. Electrolyte leakage was always higher in embryonic axes than in seeds, both in beans and groundnut, and not to have a significant effect, under the conditions studied, on germination and vigor of seedlings. The present study evidences the possibility of cryopreserving, by simple procedures, germplasm of beans and groundnut, and to verify the aging tolerance of the seeds and embryonic axes of these important species.


1970 ◽  
Vol 48 (2) ◽  
pp. 429-431 ◽  
Author(s):  
D. P. S. Verma ◽  
R. B. van Huystee

A suspension culture obtained from peanut (Arachis hypogaea L.) cotyledons was passed through three standard sieves of 0.15, 0.5, and 2.0 mm and the subsequent four fractions were studied for morphological differences and molecular heterogeneity in peroxidase isozymes. Quantitative and qualitative differences occur in this enzyme between groups of cells of different sizes. The appearance of two new peroxidase isozymes is correlated with cellular differentiation as the cell mass enlarges from 0.5 to 4.0 mm in diameter.


1992 ◽  
Vol 70 (6) ◽  
pp. 1131-1133 ◽  
Author(s):  
J. P. O'Donnell ◽  
R. B. van Huystee

Secreted peroxidase (EC 1.11.1.7) from cultured peanut (Arachis hypogaea L.) cells has two main isozymes, one cationic and one anionic. The cationic isozyme has been studied intensively owing to its greater availability. However, the several-fold lower yield of anionic peroxidase has limited study of this isozyme. In the current investigation, the yield of this isozyme from the spent medium is quantified. In addition, feedback by cationic peroxidase on its own synthesis is investigated. Key words: peanut, peroxidase, anionic, cationic, yield, feedback.


2017 ◽  
Author(s):  
Marcelo Tacán ◽  
César Tapia ◽  
César Pérez

The effects of artificial aging and cryopreservation methods on the germination of seeds and embryonic axes of Phaseolus vulgaris and Arachis hypogaea , were studied. Aging and cryopreservation treatments in bean seeds not affect the germination percentage, reaching values not significantly different from control. Germination percentage was higher when isolated embryonic axes were studied. Aging treatments gave rise to larger bean seedlings than the controls and cryopreservation treatments affected the size depending on the explant used. In groundnut seeds, aging treatments and cryopreservation positively affected germination and vigor of seedlings, but embryonic axes from not rehydrated aging seeds not germinate. Undried groundnut seeds not survive cryopreservation, while the dried ones showed a germination behavior superior to the control. Embryonic axes tolerate immersion in liquid nitrogen but when droplet-vitrification was used, formed callus instead of seedlings. Electrolyte leakage was always higher in embryonic axes than in seeds, both in beans and groundnut, and not to have a significant effect, under the conditions studied, on germination and vigor of seedlings. The present study evidences the possibility of cryopreserving, by simple procedures, germplasm of beans and groundnut, and to verify the aging tolerance of the seeds and embryonic axes of these important species.


Author(s):  
S.A. García Muñoz

Objetivo: Evaluar la germinación de cacahuate (Arachis hypogaea L.) mediante el uso de diferentes dosis de ácido giberélico (GA3). Diseño/metodología/aproximación: Se empleó un diseño completamente al azar. Se utilizaron tres tratamientos con 20 repeticiones. Tratamiento 1: 0.05gr/L de ácido giberélico (GA3), Tratamiento 2: 0.10gr/L de ácido giberélico (GA3), Tratamiento 3: 0.15gr/L de ácido giberélico (GA3) y Tratamiento 0: Testigo. Se utilizaron semillas de cacahuate de la variedad Virginia. Los parámetros a evaluar fueron, la altura de plántula, número de hojas, medida de raíz y biomasa.  Las medias fueron comparadas por la prueba de Tukey a un nivel del 5% de confianza. Resultados: Los tratamientos indicaron que el Tratamiento 0 (Testigo) obtuvo un porcentaje de germinación de 85%, siendo mayor que el tratamiento 3 (0.15gr/L de GA3) con un 75% de germinación, sin embargo, el tratamiento 1 (0.05gr/L de GA3) y 2 (0.10gr/L de GA3) presentaron una mejor respuesta al obtener un 95% de germinación cada uno. Limitaciones del estudio/implicaciones: El tratamiento 3 causa efectos negativos en la germinación de la planta. Hallazgos/conclusiones: Es necesario dar seguimiento a la investigación para un mejor control del ambiente y ampliar las dosis de GA3, así como aumentar la velocidad de germinación aplicando 0.15gr/L de GA3.


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