Submitted by Ricardo Cedraz Duque Moliterno (ricardo.moliterno@uefs.br) on 2017-04-11T21:06:17Z No. of bitstreams: 1 Tese final Ana Carolina-.pdf: 2069305 bytes, checksum: d639d8880ea9572c9a3ab7a9e940b690 (MD5) / Made available in DSpace on 2017-04-11T21:06:17Z (GMT). No. of bitstreams: 1 Tese final Ana Carolina-.pdf: 2069305 bytes, checksum: d639d8880ea9572c9a3ab7a9e940b690 (MD5) Previous issue date: 2016-09-26 / (In vitro propagation and acclimatization of medicinal species: Alpinia zerumbet (Pers.) B.L.Burtt&R.M.Sm. (Zingiberaceae) and Solidago chilensis Meyen (Asteraceae). Alpinia zerumbet and Solidago chilensis are known for their ornamental and medicinal values. There are few reports in the literature on micropropagation of Alpinia zerumbet and none about Solidago chilensis, which demonstrates the need for studies. This work aimed to study in vitro propagation of the species, involving micropropagation and developing protocols for organogenesis. For in vitro establishment were tested different types of explants, disinfestation methods and antioxidants. For multiplication, these explants were tested with plant growth regulators naftalen acetic acid and benzilaminopurin isolated and combined, and dichlorophenoxyacetic acid and kinetin, isolated and combined. It was made anatomical characterization of callus formation. For acclimatization, after pre-acclimatization, the seedlings were transferred to plastic cups containing sterilized substrate, capped with plastic bottles and taken to a greenhouse with 50% shading, where the bottle caps were unscrewed slowly. The results showed success in establishing in vitro of A. zerumbet crucial step to start large-scale cultivation. Against contamination, the most effective treatment was 4ml PPM/L (Plant Preservative Mixture), controlling 100% of pathogens. As an antioxidant, ascorbic acid (2%) was the most efficient. There was budding A. zerumbet derivatives bud explants. There was no decline in the propagation rate during in vitro subcultures, however growth is very slow. S. chilensis, explants nodal segments showed a higher rate of multiplication. There was no decline in the spread rate over four subcultures in vitro and the seedlings had a high survival rate in the acclimatization phase. / Alpinia zerumbet e Solidago chilensis s?o conhecidas pelos valores ornamental e medicinal. Existem poucos relatos na literatura sobre micropropaga??o de Alpinia zerumbet e nenhum sobre Solidago chilensis, o que demonstra necessidade de estudos. Este trabalho objetivou estudar a propaga??o in vitro das esp?cies, envolvendo micropropaga??o e desenvolvendo protocolos para organog?nese. Para o estabelecimento in vitro foram testados diferentes tipos de explantes, m?todos de desinfesta??o e antioxidantes. Para multiplica??o, esses explantes foram testados com reguladores vegetais: ?cido naftalenoac?tico e benzilaminopurina isolados e combinados, al?m de ?cido 2,4-diclorofenoxiac?tico e cinetina, isolados e combinados. Foi feita caracteriza??o anat?mica da calog?nese. Para aclimatiza??o, ap?s a pr?-aclimatiza??o, as mudas foram transferidas para copos pl?sticos contendo substrato esterilizado, tampados com garrafas pet e levados para casa de vegeta??o com sombrite 50%, onde as tampas das garrafas foram desenroscadas aos poucos. Os resultados mostraram sucesso no estabelecimento in vitro de A. zerumbet, etapa crucial para iniciar cultivo em larga escala. Contra contamina??o, o tratamento mais efetivo foi 4mL de PPM/L (Plant Preservative Mixture), controlando 100% dos pat?genos. Como antioxidante, o ?cido asc?rbico (2%) foi o mais eficiente. Houve brota??o de A. zerumbet em explantes derivados de gemas. N?o foi observado decl?nio na taxa de propaga??o no decorrer dos subcultivos in vitro, contudo o crescimento ? muito lento. Para S. chilensis, explantes de segmentos nodais apresentaram maior taxa de multiplica??o. N?o foi observado decl?nio na taxa de propaga??o no decorrer de quatro subcultivos in vitro e as mudas apresentaram alto ?ndice de sobreviv?ncia na fase de aclimatiza??o.

Submitted by Ricardo Cedraz Duque Moliterno (ricardo.moliterno@uefs.br) on 2017-10-05T21:58:20Z No. of bitstreams: 1 TESE- MARIA MAIANY DE OLIVEIRA.pdf: 1486275 bytes, checksum: 077fcda867394bf1737e7758d79af6a2 (MD5) / Made available in DSpace on 2017-10-05T21:58:20Z (GMT). No. of bitstreams: 1 TESE- MARIA MAIANY DE OLIVEIRA.pdf: 1486275 bytes, checksum: 077fcda867394bf1737e7758d79af6a2 (MD5) Previous issue date: 2017-03-29 / Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior - CAPES / Banana (Musa spp.) is considered one of the most important fruits in world trade due to its nutritional and economic potential.But although there is a large number varieties on the market, the banana is still affected by many diseases.The application of the method of crosses in this species is very difficult because the majority of cultivated varieties is triploid presenting low fertility. In this case, it is necessary to use biotechnology and its tools applied to non-conventional genetic improvement to develop new varieties that have resistance to their different types of pathogens.This work was carried out with the objective of adapting the technique of obtaining embryogeniccallus of banana by means of the Scalp method in cultivars Brazilian Ma?? and Pacovan, adjusting the processes of induction of meristematic structures and multiplication of shoots and induce increased genetic variability by in vitro mutagenesis using the chemical agent ethylmethanesulfonate and, of the genetic transformation by the bombardment of microparticles. Was evaluated the callus formation, the effect of mutagenic in the in vitro cultivation of shoots and the effects of genetic transformation on shoot resistance in selection medium containing the herbicide Imazapyr. The results showed that the merystematic structures obtained have the capacity to origin callus with only one month of cultivation, and both cultivars developed friable callus with average values above 90%.The efficiency of this method was evidenced by the high capacity of induction of friable callus in the two evaluated cultivars but also by the rapidity in the process of obtaining calluses, being the first study of adaptation of the methodology for Brazilian banana cultivars.On the other hand, the evaluation of the mutation induction allowed to conclude that the survival and the capacity of bud formation decreased as a function of the increase of the concentration and the immersion time in the ethylmethanesulfonate.The surviving plants underwent a sorting with the fusaric acid selective agent in which it was possible to regenerate in vitro plants of the cultivars submitted to treatment with the mutagen and to select possible mutants with fusaric acid resistance for cultivarsMa?? and Pacovan.And the genetic transformation method proved efficient in the regeneration of shoots resulting in high values of survival and multiplication, where possible transgenic plants of banana cv. Ma?? were obtained after selection of resistance to the herbicide.Therefore, it is concluded that all the material produced, both in the mutagenic phase and in the genetic transformation, presents a greater genetic variability potentially applicable to the banana improvement. / A banana (Musa spp.) ? considerada um dos mais importantes frutos no com?rcio mundial em virtude seu potencial nutritivo e econ?mico. Mas, apesar de existir um grande n?mero de variedades no mercado, a bananeira ainda ? acometida por muitas doen?as. A aplica??o do m?todo de cruzamentos nesta esp?cie ? muito dif?cil, pois a maioria das variedades cultivadas ? triploide apresentando baixa fertilidade. Nesse caso, faz-se necess?rio o uso da biotecnologia e de suas ferramentas aplicadas ao melhoramento gen?tico n?o convencional para desenvolver novas variedades que tenham resist?ncia aos seus diferentes tipos de pat?genos. Este trabalho foi realizado com os objetivos de adaptar a t?cnica de obten??o de calos embriog?nicos de bananeira por meio do m?todo Scalp nas cvs. Ma?? e Pacovan, ajustando os processos de indu??o de estruturas polimeristem?ticas ede multiplica??o de brotos e induzir o aumento da variabilidade gen?tica por meio da mutag?nese in vitro com o uso do agente qu?mico etilmetanosulfonato e, da transforma??o gen?tica pelo bombardeamento de micropart?culas.Foram avaliados os calos formados, o efeito do mutag?nico no cultivo in vitro de brotos e, os efeitos da transforma??o gen?tica quanto ? resist?ncia dos brotos em meio de sele??o contendo o herbicida Imazapyr. Os resultados mostraram que as estruturas polimeristem?ticas obtidas t?m capacidade de originar calos com apenas um m?s de cultivo e, ambas as cultivares desenvolveram calos fri?veis com rendimentos m?dios acima de 90%. A efici?ncia desse m?todo foi comprovada pela alta capacidade de indu??o de calos fri?veis nas duas cultivares avaliadas, como tamb?m pela rapidez no processo de obten??o de calos, sendo este o primeiro estudo de adapta??o da metodologia para as cultivares Ma?? e Pacovan. Por outro lado, a avalia??o da indu??o de muta??o permitiu concluir que a sobreviv?ncia e a capacidade de forma??o de brotos diminu?ram em fun??o do aumento da concentra??o e do tempo de imers?o no etilmetanosulfonato. As plantas sobreviventes passaram por uma triagem com o agente seletivo ?cido fus?rico na qual, foi poss?vel regenerar plantas in vitro das cultivares submetidas ao tratamento com o mutag?nico e selecionar poss?veis mutantes com resist?ncia ao ?cido fus?rico para as cvs. Ma?? e Pacovan. O m?todo da transforma??o gen?tica mostrou-se eficiente na regenera??o dos brotos resultando em altos valores de sobreviv?ncia e multiplica??o, onde poss?veis plantas transg?nicas de bananeira cv. Ma?? foram obtidas, ap?s a sele??o de resist?ncia ao herbicida. Portanto, conclui-se que todo material produzido, tanto na fase mutag?nica quanto na transforma??o gen?tica, apresenta uma maior variabilidade gen?tica potencialmente aplic?vel ao melhoramento da bananeira.

Submitted by Jadson Francisco de Jesus SILVA (jadson@uefs.br) on 2018-01-30T22:51:06Z No. of bitstreams: 1 Tese Definitivo ZERGurgel.pdf: 2392487 bytes, checksum: 97870ae444449d037535f874c18b1d37 (MD5) / Made available in DSpace on 2018-01-30T22:51:06Z (GMT). No. of bitstreams: 1 Tese Definitivo ZERGurgel.pdf: 2392487 bytes, checksum: 97870ae444449d037535f874c18b1d37 (MD5) Previous issue date: 2017-07-24 / Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior - CAPES / Comanthera mucugensis Giul. subsp. mucugensis, an endemic species of the municipality of Mucug?-BA is threatened with extinction. To reduce extractivism in natural populations, it is necessary to develop efficient multiplication protocols; In this sense somatic embryogenesis and organogenesis may be viable and preservation cryopreservation may be a strategy for its long-term. The objectives of this study were: (1) to analyze the embryogenic competence and the indirect organogenesis of C. mucugensis; (2) to evaluate the cryopreservation of seeds and different methods of cryopreservation of C. mucugensis plants and (3) to identify the best way to store seeds in the long term. Experiments were performed to induce somatic embryogenesis with different concentrations of 2,4-D X BAP and Picloran X BAP and for indirect organogenesis BAP and ANA were used. Seeds were cryopreserved for 0 (control), 1, 7, 30, 360 and 540 days and other seeds were stored at different temperatures to verify the best form of storage. Plants were cryopreserved with the technique of vitrification and encapsulation-desiccation. Plants from cryopreserved seeds were acclimatized in sand and vegetal soil (1: 1) for 60 days. The work showed that the plant regulators Picloran and 2,4-D are promising in the induction of callus with embryogenic potential and that the plant regulator ANA at 4.9 ?M is efficient in indirect organogenesis. The seeds of C. mucugensis can be cryopreserved without compromising their physiological quality, but the techniques for cryopreservation of plants have not been efficient. / Comanthera mucugensis Giul. subsp. mucugensis, possui flor de interesse comercial que devido ao extrativismo excessivo encontra-se amea?ada de extin??o. Para suprir a demanda do mercado e evitar o decl?nio populacional, faz-se necess?rio desenvolver protocolos para sua multiplica??o, podendo a embriog?nese som?tica e a organog?nese serem alternativas vi?veis. Al?m disso, ? importante investir em estudos de conserva??o a longo prazo como, por exemplo, a criopreserva??o. O trabalho teve como objetivos: realizar estudos para tornar a micropropaga??o mais eficiente e avaliar a conserva??o de C. mucugensis em diferentes temperaturas como estrat?gia para a conserva??o do seu germoplasma. Foram testados para a indu??o da embriog?nese som?tica 2,4-D x BAP e Picloram x BAP e para organog?nese indireta BAP e ANA. Na criopreserva??o foram avaliadas sementes mantidas em nitrog?nio l?quido (-196?C) por 0, 1, 7, 30, 360 e 540 dias e as plantas inteiras foram submetidas a duas t?cnicas: vitrifica??o e encapsulamento-desidrata??o. Para avaliar o armazenamento, as sementes foram mantidas em temperatura ambiente, 4?C, -20?C, -80?C e -196?C por 30, 90 e 180 dias. Visando observar se a criopreserva??o das sementes interfere no desenvolvimento, plantas oriundas da germina??o in vitro de sementes criopreservadas foram aclimatizadas em areia e terra vegetal (1:1) por 60 dias. O trabalho demonstrou que os reguladores vegetais Picloram e 2,4-D s?o promissores na indu??o de calos com potencial embriog?nico e que o regulador vegetal ANA (4,9 ?M) ? eficiente na organog?nese indireta. As sementes de C. mucugensis podem ser criopreservadas sem comprometer sua qualidade fisiol?gica, entretanto, n?o foram eficientes as t?cnicas para criopreserva??o de plantas inteiras.

Submitted by Natalie Mendes (nataliermendes@gmail.com) on 2015-08-04T01:30:32Z No. of bitstreams: 1 CRIS TESE FINAL.pdf: 3970188 bytes, checksum: 37240b01333f3a3c2c98ce2597450f53 (MD5) / Made available in DSpace on 2015-08-04T01:30:32Z (GMT). No. of bitstreams: 1 CRIS TESE FINAL.pdf: 3970188 bytes, checksum: 37240b01333f3a3c2c98ce2597450f53 (MD5) Previous issue date: 2015-03-13 / Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior - CAPES / The life cycle of a seed plant involves subsequent stages of development including seed formation, germination and seedling establishment. Together these stages represent the critical phase of intersection between two generations and are characterized by deep cytological, morphological, metabolic and physiological changes. Jatropha curcas L. (Euphorbiaceae) is popularly known as physic nut and produces seeds rich in oil with properties that allow its use in various industries, including the production of biodiesel. This study aimed to advance on the understanding of morphophysiological patterns and elucidate morphoanatomical adaptations involving embryogenesis, maturation, germination and seedling growth in J. curcas. Therefore, it was initially analysed and described the morphophysiological profile based on 13 stages of development and maturation associated to color of the fruit exocarp and seed coat, and description of the structures present at each stage (Chapter 1). Analysis of microtubular cytoskeleton configurations during embryogenesis showed cell cycle activity by the presence of cortical and mitotic microtubules during histodifferentiation and organogenesis, whilst it was possible to characterize a new organogenetic profile of embryogenesis revealed by the presence of a multimeristematic radicle and stomata in embryos of J. curcas seeds (Chapter 2). The multimeristematic embryos formed by a central apical meristem and four lateral meristems interconnected by a complex vascular system have revealed a new model of root formation during seed germination and seedling development, in which there is simultaneous protrusion of a larger main root and four smaller adventitious roots, all growing at the same time during the formation of the seedling root system (Chapter 3). The stomata occurred in the radicle-hypocotyl transition area, exhibited different sizes and ontogenic phases and short lifespan by degenerating during seedling development. This demonstrates it?s functioning as restricted to the simultaneous growth stage of the five roots during germination, apparently due to high demand in gas exchange and energy metabolism, and a likely evolution onto the lenticels present in the stem of this species (Chapter 4). / O ciclo de vida de uma planta com sementes envolve est?dios subsequentes de desenvolvimento, como a forma??o da semente, a germina??o e o estabelecimento da pl?ntula. Essas etapas juntas representam a fase cr?tica de interse??o entre duas gera??es e s?o caracterizadas por profundas mudan?as citol?gicas, morfol?gicas, metab?licas e fisiol?gicas. Jatropha curcas L. (Euphorbiaceae) conhecida popularmente como pinh?o-manso, produz sementes ricas em ?leo com propriedades e aplica??es em diversos setores industriais, incluindo a produ??o de biodiesel. O presente estudo teve como objetivo caracterizar padr?es morfofisiol?gicos e elucidar adapta??es morfoanat?micas envolvendo a embriog?nese, matura??o, germina??o e o crescimento de pl?ntulas de J. curcas. Para tanto, foi inicialmente analisado e descrito o perfil morfofisiol?gico baseado em 13 est?dios de desenvolvimento e matura??o, associados ? colora??o do exocarpo do fruto e do tegumento das sementes e descri??o das estruturas presentes em cada est?dio (Cap?tulo 1). A an?lise das configura??es do citoesqueleto microtubular durante embriog?nese evidenciou atividade do ciclo celular por meio da presen?a de microt?bulos corticais e mit?ticos durante a histodiferencia??o e organog?nese. Foi poss?vel caracterizar um novo padr?o organogen?tico de embriog?nese revelado pela presen?a de rad?cula multimeristem?tica e de est?matos em embri?es de sementes de J. curcas (Cap?tulo 2). Os embri?es multimeristem?ticos, providos de um meristema apical central e quatro meristemas laterais, revelaram um novo modelo de forma??o de sistema radicular durante a germina??o de sementes e desenvolvimento de pl?ntulas, em que h? protrus?o simult?nea de uma raiz principal maior e quatro ra?zes advent?cias menores, todas crescendo ao mesmo tempo, durante a forma??o inicial do sistema radicular da pl?ntula (Cap?tulo 3). Os est?matos ocorrem na ?rea de transi??o hipoc?tilo-rad?cula e exibem diferentes tamanhos e fases ontog?nicas. Estas estruturas apresentaram um curto per?odo de vida, degenerando-se durante o desenvolvimento da pl?ntula, sugerindo seu funcionamento restrito ? etapa de crescimento simult?neo das cinco ra?zes durante a germina??o, aparentemente devido ? alta demanda em trocas gasosas e metabolismo energ?tico, e uma prov?vel evolu??o para as lenticelas presentes no caule desta esp?cie (Cap?tulo 4).

Submitted by Ricardo Cedraz Duque Moliterno (ricardo.moliterno@uefs.br) on 2015-10-08T22:13:49Z No. of bitstreams: 1 Disserta??o Final_Fabio Ribeiro Garcia.pdf: 1235311 bytes, checksum: 99c4c15b4044b2e3d060b0f7f4d595d4 (MD5) / Made available in DSpace on 2015-10-08T22:13:49Z (GMT). No. of bitstreams: 1 Disserta??o Final_Fabio Ribeiro Garcia.pdf: 1235311 bytes, checksum: 99c4c15b4044b2e3d060b0f7f4d595d4 (MD5) Previous issue date: 2013-05-07 / Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior - CAPES / bromeliad species are native to Brazil and have great potential for use as an ornamental plant, and a relevant ecological importance. Considering the devastation of the Atlantic, currently 7.3% of its original area preserved and where about 70% are endemic bromeliad is important to establish methods of propagation and ex situ conservation in order to preserve this germplasm and avoid irreversible genetic erosion. Thus, the aim of this work was to establish protocols and micropropagation in vitro conservation of A. blancheteana and A. miniata. In the first chapter, for multiplication in vitro, we used different concentrations of BAP and for rooting tested different concentrations of auxins IAA, IBA and NAA. In the second chapter we tested two protocols, was first used in MS medium supplemented with different concentrations of auxin Picloram and 2,4-D combined with BAP and the second experiment evaluated MS medium supplemented with 2,4-D or picloram in different concentrations. In the third chapter, we investigated the effect of osmotic agents, sucrose, sorbitol and mannitol in vitro conservation A. blancheteana. For the best result micropropagation for multiplication was for medium supplemented with 4.44 ?M BA. To induce somatic embryos and regeneration of the concentration of 22.5 ?M 2,4-D was the most efficient. Independent of concentration, mannitol was more efficient for in vitro conservation of A. blancheteana for 12 months. / Aechmea blancheteana (Baker) L.B. Smith e Aechmea miniata (Beer) Baker s?o esp?cies de brom?lias nativas do Brasil que possuem grande potencial para uso como planta ornamental, al?m de relevante import?ncia ecol?gica. Considerando a grande devasta??o de Mata Atl?ntica, atualmente com 7,3% de sua ?rea original preservada, onde cerca de 70% das brom?lias s?o end?micas ? importante o estabelecimento de m?todos propaga??o e conserva??o ex situ com o objetivo de preservar esse germoplasma e evitar uma eros?o gen?tica irrevers?vel. Assim, o objetivo deste trabalho estabelecer os protocolos de micropropaga??o e conserva??o in vitro de A. blancheteana e A. miniata. No primeiro cap?tulo, para a multiplica??o in vitro, foram utilizadas diferentes concentra??es de BAP e na fase de enraizamento foram testadas diferentes concentra??es das auxinas AIA, AIB e ANA. No segundo cap?tulo foram testadas a combina??o de diferentes concentra??es das auxinas Picloram e 2,4-D e da auxina 2,4-D combinada com a citocinina BAP na indu??o de embri?es som?ticos. No terceiro cap?tulo, foi avaliado o efeito dos agentes osm?ticos, sacarose, sorbitol e manitol na conserva??o in vitro de A. blancheteana. Para a micropropaga??o o melhor resultado foi obtido em meio MS suplementado com 4,44?M de BAP. Para a indu??o e regenera??o de embri?es som?ticos, a concentra??o 22,5?M de 2,4-D foi a mais eficiente. Independente da concentra??o, o manitol foi mais eficiente para a conserva??o in vitro de A. blancheteana por 12 meses.