Procesos biotecnológicos In Vitro para la formación de callos a partir de tejidos foliares de cafeto (Coffea arabica L.)

This research study included both field and laboratory work during the period between May 2015 and January 2016. The field work entailed the gathering of vegetal material from a coffee sector of the Nambacola parish, which is part of the canton of Gonzanamá in the province of Loja. In a Plant Microp...

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Autor principal: Diaz Sigcho, Tania del Pilar (author)
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Publicado: 2019
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author Diaz Sigcho, Tania del Pilar
author_facet Diaz Sigcho, Tania del Pilar
author_role author
collection Repositorio Universidad Nacional de Loja
dc.contributor.none.fl_str_mv Encalada Córdova, Max
dc.creator.none.fl_str_mv Diaz Sigcho, Tania del Pilar
dc.date.none.fl_str_mv 2019-01-16T15:05:31Z
2019-01-16T15:05:31Z
2019-01-16
dc.format.none.fl_str_mv 45 p.
application/pdf
dc.identifier.none.fl_str_mv http://dspace.unl.edu.ec/jspui/handle/123456789/21596
dc.language.none.fl_str_mv spa
dc.publisher.none.fl_str_mv Loja
dc.rights.none.fl_str_mv http://creativecommons.org/licenses/by-nc-sa/3.0/ec/
info:eu-repo/semantics/openAccess
dc.source.none.fl_str_mv reponame:Repositorio Universidad Nacional de Loja
instname:Universidad Nacional de Loja
instacron:UNL
dc.subject.none.fl_str_mv CAFE
COFFEA ARABICA
IN VITRO
dc.title.none.fl_str_mv Procesos biotecnológicos In Vitro para la formación de callos a partir de tejidos foliares de cafeto (Coffea arabica L.)
dc.type.none.fl_str_mv info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/bachelorThesis
description This research study included both field and laboratory work during the period between May 2015 and January 2016. The field work entailed the gathering of vegetal material from a coffee sector of the Nambacola parish, which is part of the canton of Gonzanamá in the province of Loja. In a Plant Micropropagation Laboratory, two study phases were carried out, which included the disinfection of the plant material brought from the field as well as the application of auxins and cytokinins for the formation of calluses. In the first lab phase of disinfection, three concentrations of calcium hypochlorite were applied (15, 20 and 25%) in two immersion times (10 and 20 min), which produced a completely random design with a factorial arrangement of 3x2, six treatments, and three repetitions that evaluated the contamination of the explants. The analysis displayed an interaction between calcium hypochlorite and the immersion time, this determined that the treatment with the lowest percentage of contamination was T5 (25% Ca (ClO) 2 + 10 min) with a value of 37.62% with significant differences compared to T2 (15% Ca (ClO) 2 + 20 min) and T4 (20% Ca (ClO) 2 + 20 min), which showed a contamination of 86.19% and 74.76% respectively. T1, T3, and T6 treatments did not show significant differences in percentage of contamination. In the second lab phase, which was about in vitro callus formation of explants, a mixture of two growth hormones was used, namely, auxin: 2,4-dichlorophenoxyacetic acid (2,4-D) in concentrations of 1.0; 3.0; 3.0 and 6.0 ppm and a cytokinin: benziladenine (BAP) in three concentrations of 3.0; 10.0; 0.0 and 0.0 ppm ppm respectively. Also, a completely randomized design was established, where callus formation was evaluated in explants of Coffea arabica L. The treatment with the highest percentage of callus was T1 (1.0 ppm 2,4-D +3.0 ppm BAP), which was obtained through the analysis of variance (ANOVA) that determined that the treatments they presented high variability among them. In the same way the Tukey test showed significant differences between treatments with a p = <0.05. It should be noted that treatments without cytokinins (BAP) did not present callus formation. According to the days evaluated, the appearance of stranding was evident on the twentieth day of evaluation for treatments T1 and T2 with percentages of 60 and 20% respectively, while T3 and T4 did not present any value for this indicator. Stranding was stabilized at 30 days of evaluation in T1 and T2 reaching values of 73.33 and 26.67% respectively, on the other hand treatments T3 and T4 did not present callus formation. The calluses obtained showed homogenous as well as an inhomogeneous formation. For instance, the explants that formed calluses in T1 (1.0 ppm 2,4-D +3.0 ppm BAP) presented percentage values of 66.7 and 33.33 of homogenous and inhomogeneous callus respectively when comparing to T2 (3.0 ppm 2,4-D +10.0 ppm BAP) which presented a 100% non-homogeneous callus. In the present research work, disinfection and in vitro propagation protocols were generated in the Coffea arabica L. species, to contribute toward future in vitro studies for the of coffee trees. Keywords: Coffea arabica L., in vitro, spread.
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spelling Procesos biotecnológicos In Vitro para la formación de callos a partir de tejidos foliares de cafeto (Coffea arabica L.)Diaz Sigcho, Tania del PilarCAFECOFFEA ARABICAIN VITROThis research study included both field and laboratory work during the period between May 2015 and January 2016. The field work entailed the gathering of vegetal material from a coffee sector of the Nambacola parish, which is part of the canton of Gonzanamá in the province of Loja. In a Plant Micropropagation Laboratory, two study phases were carried out, which included the disinfection of the plant material brought from the field as well as the application of auxins and cytokinins for the formation of calluses. In the first lab phase of disinfection, three concentrations of calcium hypochlorite were applied (15, 20 and 25%) in two immersion times (10 and 20 min), which produced a completely random design with a factorial arrangement of 3x2, six treatments, and three repetitions that evaluated the contamination of the explants. The analysis displayed an interaction between calcium hypochlorite and the immersion time, this determined that the treatment with the lowest percentage of contamination was T5 (25% Ca (ClO) 2 + 10 min) with a value of 37.62% with significant differences compared to T2 (15% Ca (ClO) 2 + 20 min) and T4 (20% Ca (ClO) 2 + 20 min), which showed a contamination of 86.19% and 74.76% respectively. T1, T3, and T6 treatments did not show significant differences in percentage of contamination. In the second lab phase, which was about in vitro callus formation of explants, a mixture of two growth hormones was used, namely, auxin: 2,4-dichlorophenoxyacetic acid (2,4-D) in concentrations of 1.0; 3.0; 3.0 and 6.0 ppm and a cytokinin: benziladenine (BAP) in three concentrations of 3.0; 10.0; 0.0 and 0.0 ppm ppm respectively. Also, a completely randomized design was established, where callus formation was evaluated in explants of Coffea arabica L. The treatment with the highest percentage of callus was T1 (1.0 ppm 2,4-D +3.0 ppm BAP), which was obtained through the analysis of variance (ANOVA) that determined that the treatments they presented high variability among them. In the same way the Tukey test showed significant differences between treatments with a p = <0.05. It should be noted that treatments without cytokinins (BAP) did not present callus formation. According to the days evaluated, the appearance of stranding was evident on the twentieth day of evaluation for treatments T1 and T2 with percentages of 60 and 20% respectively, while T3 and T4 did not present any value for this indicator. Stranding was stabilized at 30 days of evaluation in T1 and T2 reaching values of 73.33 and 26.67% respectively, on the other hand treatments T3 and T4 did not present callus formation. The calluses obtained showed homogenous as well as an inhomogeneous formation. For instance, the explants that formed calluses in T1 (1.0 ppm 2,4-D +3.0 ppm BAP) presented percentage values of 66.7 and 33.33 of homogenous and inhomogeneous callus respectively when comparing to T2 (3.0 ppm 2,4-D +10.0 ppm BAP) which presented a 100% non-homogeneous callus. In the present research work, disinfection and in vitro propagation protocols were generated in the Coffea arabica L. species, to contribute toward future in vitro studies for the of coffee trees. Keywords: Coffea arabica L., in vitro, spread.La presente investigación se desarrolló en el campo y una fase de laboratorio dentro el período comprendido entre mayo 2015 enero 2016. En el campo se realizó la recolección del material vegetal en un sector cafetalero de la parroquia Nambacola perteneciente al cantón Gonzanamá de la provincia Loja. En el laboratorio de micropropagación vegetal se llevó a cabo dos fases de laboratorio las cuales comprendieron la desinfección del material vegetal traído del campo y la segunda fase en la aplicación de auxinas y citoquininas para la formación de callos. Para la primera fase de desinfección se aplicó hipoclorito de calcio en tres concentraciones (15, 20 y 25 %) y en dos tiempos de inmersión (10 y 20 min), estableciendo un diseño completamente al azar con un arreglo factorial de 3x2, con seis tratamientos y tres repeticiones evaluando la contaminación de los explantes. El análisis mostró interacción entre el hipoclorito de calcio y el tiempo de inmersión, obteniendo el tratamiento con menor porcentaje de contaminación el T5 (25 % Ca (ClO)2 + 10 min) con valor de 37,62 % con diferencias significativas frente al T2 (15 % Ca (ClO)2 + 20 min) y T4 (20 % Ca (ClO)2 + 20 min), que presentaron una contaminación de 86,19 %; 74,76 % respectivamente. Destacando que los tratamientos T1, T3, Y T6 no mostraron diferencias significativas de porcentaje de contaminación. En la segunda fase para a la formación de callos in vitro de explantes, se utilizó la mezcla de dos hormonas de crecimiento, la auxina: 2,4-ácido diclorofenoxiacético (2,4 -D) en concentraciones de 1,0; 3,0; 3,0 y 6,0 ppm y una citoquinina: benziladenina (BAP), en tres concentraciones 3,0; 10,0; 0,0 y 0,0 ppm respectivamente, para lo cual se estableció un diseño completamente al azar, donde se evaluó la formación de callo en explantes de Coffea arabica L. El tratamiento con mayor porcentaje de callo fue el T1 (1,0 ppm 2,4-D +3,0 ppm BAP), el cual se lo obtuvo mediante el análisis de varianza (ANOVA) que determino que los tratamientos presentaron alta variabilidad entre ellos. De la misma manera la prueba de Tukey, mostró diferencias significativas entre tratamientos con una p = < 0,05. Cabe destacar que los tratamientos sin citoquininas (BAP) no presentaron formación de callo. Según los días evaluados la aparición de encallamiento se evidenció al veinteavo día de evaluación para los tratamientos T1 y T2 con porcentajes del 60 y 20 % respectivamente, mientras que los T3 y T4 no presentaron ningún valor para este indicador. El encallamiento se estabilizó a los 30 días de evaluación en los T1 y T2 llegando a alcanzar valores de 73,33 y 26,67 % respectivamente, por otro lado los tratamientos T3 y T4 no se presentaron formación de callos. Los callos obtenidos mostraron formación homogénea y no homogénea, tomando en cuenta solo los explantes que formaron callos presentando porcentajes en el T1 (1,0 ppm 2,4-D +3,0 ppm BAP) valores de 66,7 y 33,33 de callo homogéneo y no homogéneo respectivamente, frente al T2 (3,0 ppm 2,4-D +10,0 ppm BAP) que presentó un 100 % de callo no homogéneo. En el presente trabajo de investigación se generaron protocolos de desinfección y propagación in vitro en la especie Coffea arabica L., para contribuir con estudios para futuras investigaciones in vitro en la propagación de cafeto. Palabras clave: Coffea arabica L., in vitro, propagación.LojaEncalada Córdova, Max2019-01-16T15:05:31Z2019-01-16T15:05:31Z2019-01-16info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/bachelorThesis45 p.application/pdfhttp://dspace.unl.edu.ec/jspui/handle/123456789/21596spahttp://creativecommons.org/licenses/by-nc-sa/3.0/ec/info:eu-repo/semantics/openAccessreponame:Repositorio Universidad Nacional de Lojainstname:Universidad Nacional de Lojainstacron:UNL2025-05-02T15:46:31Zoai:dspace.unl.edu.ec:123456789/21596Institucionalhttps://dspace.unl.edu.ec/Universidad públicahttps://unl.edu.ec/https://dspace.unl.edu.ec/oaiEcuador***opendoar:02025-05-02T15:46:31falseInstitucionalhttps://dspace.unl.edu.ec/Universidad públicahttps://unl.edu.ec/https://dspace.unl.edu.ec/oai*Ecuador***opendoar:02025-05-02T15:46:31Repositorio Universidad Nacional de Loja - Universidad Nacional de Lojafalse
spellingShingle Procesos biotecnológicos In Vitro para la formación de callos a partir de tejidos foliares de cafeto (Coffea arabica L.)
Diaz Sigcho, Tania del Pilar
CAFE
COFFEA ARABICA
IN VITRO
status_str publishedVersion
title Procesos biotecnológicos In Vitro para la formación de callos a partir de tejidos foliares de cafeto (Coffea arabica L.)
title_full Procesos biotecnológicos In Vitro para la formación de callos a partir de tejidos foliares de cafeto (Coffea arabica L.)
title_fullStr Procesos biotecnológicos In Vitro para la formación de callos a partir de tejidos foliares de cafeto (Coffea arabica L.)
title_full_unstemmed Procesos biotecnológicos In Vitro para la formación de callos a partir de tejidos foliares de cafeto (Coffea arabica L.)
title_short Procesos biotecnológicos In Vitro para la formación de callos a partir de tejidos foliares de cafeto (Coffea arabica L.)
title_sort Procesos biotecnológicos In Vitro para la formación de callos a partir de tejidos foliares de cafeto (Coffea arabica L.)
topic CAFE
COFFEA ARABICA
IN VITRO
url http://dspace.unl.edu.ec/jspui/handle/123456789/21596