Oat development in response to temperature / Desenvolvimento de aveia em respostaà temperatura

ABSTRACT: Temperature affects plant development therefore phyllochron has been used as a predictor for developmental events to define the time for agricultural managing practices. This study aims to evaluate changes in phyllochron and thermal sum required for flowering by oat genotypes developed at different decades at three temperature regimes; the effect of high temperature on phytomere development; and identify the development stage at the moment of meristem transition to reproductive stage. Three environments were obtained by sowing in the fall, in the spring, and under constant temperature (17oC), always at inductive photoperiod. Despite changes in nominal values small differences were found among genotypes' phyllochron. Adding specific optimal and maximum temperatures into the growing degree days' calculation demonstrated phyllochron stability among environments. Plant cycle length and thermal sum correlated with the number of developed phytomeres. UFRGS 078030-2 plants flowered earlier, had a small number of phytomeres, and greater tolerance to elevated temperatures than the other genotypes. More recent genotypes transit to reproductive stage at an earlier Haun stage than older ones.

RESUMO: A temperatura afeta o desenvolvimento das plantas, portanto o filocrono tem sido usado para prever eventos de desenvolvimento e estabelecer o momento adequado para práticas agrícolas. Esse estudo buscou avaliar mudanças em filocrono e soma térmica até o florescimento de genótipos de aveia desenvolvidos em diferentes décadas em três regimes térmicos; o efeito de altas temperaturas no desenvolvimento de fitômeros; e identificar o estágio de desenvolvimento em que ocorre a transição do meristema para a fase reprodutiva. Três ambientes foram estabelecidos pela semeadura no outono, na primavera e em temperatura constante (17oC), em fotoperíodo indutor. Apesar da alteração dos valores numéricos, houve pouca diferença entre os filocronos dos genótipos. A adição das temperaturas ótima e máxima específicas no cálculo de graus dias demonstrou a estabilidade de filocrono entre ambientes. O ciclo e a soma térmica correlacionaram-se com o número de fitômeros. UFRGS 078030-2 floresceu mais cedo, teve menos fitômeros e maior tolerância a altas temperaturas do que os demais genótipos. Os genótipos mais recentes transitam para a fase reprodutiva em estágios mais precoces da escala Haun, em comparação com os genótipos mais antigos.

Bioinformatics analysis and function prediction of ginseng TCP transcription factor family / 中国中药杂志

The longevity mechanism of ginseng(Panax ginseng) is related to its strong meristematic ability. In this paper, this study used bioinformatic methods to identify the members of the ginseng TCP gene family in the whole genome and analyzed their sequence characteristics. Then, quantitative real-time fluorescent PCR was performed to analyze the TCP genes containing elements rela-ted to meristem expression in the taproots, fibrous roots, stems, and leaves. According to the data, this study further explored the expression specificity of TCP genes in ginseng tissues, which facilitated the dissection of the longevity mechanism of ginseng. The ginseng TCP members were identified and analyzed using PlantTFDB, ExPASy, MEME, PLANTCARE, TBtools, MEGA and DNAMAN. The results demonstrated that there were 60 TCP gene family members in ginseng, and they could be divided into two classes: Class Ⅰ and Class Ⅱ, in which the Class Ⅱ possessed two subclasses: CYC-TCP and CIN-TCP. The deduced TCP proteins in ginseng had the length of 128-793 aa, the isoelectric point of 4.49-9.84 and the relative molecular mass of 14.2-89.3 kDa. They all contained the basic helix-loop-helix(bHLH) domain. There are a variety of stress response-related cis-acting elements in the promoter regions of ginseng TCP genes, and PgTCP20-PgTCP24 contained the elements associated with meristematic expression. The transcription levels of PgTCP20-PgTCP24 were high in fibrous roots and leaves, but low in stems, indicating the tissue-specific expression of ginseng TCP genes. The Class Ⅰ TCP members which contained PgTCP20-PgTCP23, may be important regulators for the growth and development of ginseng roots.

Genes involved in the deformations of the shoot apical meristem in somatic embryos of Capsicum chinense Jacq.

Somatic embryos (SE) of habanero pepper (Capsicum chinense Jacq.) represent persistent deformations in the shoot apical meristem (SAM), which inhibits their capacity to form organs and subsequently plants. In dicotyledonous plants, SAM is formed in the apex, between cotyledons and it plays a central role in postembryonic shoot organ formation. Based on the previous knowledge on the role of some families of gene in the formation, organization and maintenance of the SAM, the expression patterns of WUS, WOX2, NAM, STM, PIN1 and PIN7 genes were analysed, which would allow us to elucidate the possible implication of these genes in SAM deformations in the SE of C. chinense. The results show that the expression patterns of STM and PIN1 in the SE were completely opposite to the respective expression pattern obtained in zygotic embryos (ZE). Moreover, NAM and PIN7 showed an over accumulation of transcripts in SE, compared with ZE. This is the first time in the genus Capsicum that alterations in the expression pattern of key genes of the SE development are reported, as well as its possible implication in the persistent deformations of the SAM.

Advances in plant stem cell culture / 生物工程学报

Plant stem cells are the cells that are located in meristems and are kept in a state of undifferentiation. Plant stem cell possesses lower vacuolization, higher mitochondrial activity, more genetic stability and stronger self-renewal capacity compared with calli. Plant stem cell culture has a wide application in pharmaceutical, functional food as well as cosmetic industries. Here we describe the procedure of induction, isolation and identification of plant stem cells, to provide a reference for further research in this field.

Processed fruit juice ready to drink: screening acute toxicity at the cellular level / Sucos de frutas industrializados prontos para consumo: screening da toxicidade aguda em nível celular

The present study evaluated the acute toxicity at the cellular level of processed juice ready for consumption Orange and Grape flavors, produced by five companies with significant influence on the food market of South American countries, especially in Brazil. This evaluation was performed in root meristem cells of Allium cepa L., at the exposure times of 24 and 48 hours, directly with marketed liquid preparations. Based on the results, it was found that fruit juices, of all companies considered, promoted significant antiproliferative effect to root meristems at the exposure time of 24 hours and resulted in at both exposure times, statistically significant number of mitotic spindle changes and chromosomal breaks. Therefore, under the study conditions, all juice samples analyzed were cytotoxic, genotoxic and mutagenic to root meristem cells. These results indicate that such beverages have relevant potential to cause cellular disorders and, thus, need to be evaluated more fully in more complex test systems, as those in rodents, and then establish specific toxicity at the cellular level of these juices and ensure the well-being of those who consume them.

Objetivou-se neste trabalho avaliar a toxicidade aguda em nível celular de sucos industrializados prontos para beber, sabor laranja e uva, de cinco empresas alimentícias de reconhecida reputação no mercado de alimentos em países da América do Sul, especialmente o Brasil. Esta avaliação se deu por meio das células meristemáticas de raízes de Allium cepa L., nos tempos de exposição 24 e 48h, diretamente nos preparados líquidos comercializados. Com base nos resultados obtidos verificou-se que os sucos de frutas, de todas as empresas consideradas, promoveram expressivo efeito antiproliferativo aos meristemas de raízes já no tempo de exposição 24h, e ocasionaram número estatisticamente significativo de alterações de fuso mitótico e quebras cromossômicas nas células do tecido analisado em todo o tempo de análise. Portanto, nas condições de estudo estabelecidas, os sucos das empresas avaliadas foram citotóxicos, genotóxicos e mutagênicos. Estes resultados são importantes em razão de indicarem que tais alimentos têm relevante potencial em causar distúrbios celulares e, portanto, devem ser avaliados em sistemas com testes mais complexo, como os em roedores, para, dessa forma, estabelecer com propriedade a toxicidade em nível celular desses alimentos e assegurar o bem-estar daqueles que os consomem.

Processed fruit juice ready to drink: screening acute toxicity at the cellular level / Sucos de frutas industrializados prontos para consumo: screening da toxicidade aguda em nível celular

The present study evaluated the acute toxicity at the cellular level of processed juice ready for consumption Orange and Grape flavors, produced by five companies with significant influence on the food market of South American countries, especially in Brazil. This evaluation was performed in root meristem cells of Allium cepa L., at the exposure times of 24 and 48 hours, directly with marketed liquid preparations. Based on the results, it was found that fruit juices, of all companies considered, promoted significant antiproliferative effect to root meristems at the exposure time of 24 hours and resulted in at both exposure times, statistically significant number of mitotic spindle changes and chromosomal breaks. Therefore, under the study conditions, all juice samples analyzed were cytotoxic, genotoxic and mutagenic to root meristem cells. These results indicate that such beverages have relevant potential to cause cellular disorders and, thus, need to be evaluated more fully in more complex test systems, as those in rodents, and then establish specific toxicity at the cellular level of these juices and ensure the well-being of those who consume them.

Objetivou-se neste trabalho avaliar a toxicidade aguda em nível celular de sucos industrializados prontos para beber, sabor laranja e uva, de cinco empresas alimentícias de reconhecida reputação no mercado de alimentos em países da América do Sul, especialmente o Brasil. Esta avaliação se deu por meio das células meristemáticas de raízes de Allium cepa L., nos tempos de exposição 24 e 48h, diretamente nos preparados líquidos comercializados. Com base nos resultados obtidos verificou-se que os sucos de frutas, de todas as empresas consideradas, promoveram expressivo efeito antiproliferativo aos meristemas de raízes já no tempo de exposição 24h, e ocasionaram número estatisticamente significativo de alterações de fuso mitótico e quebras cromossômicas nas células do tecido analisado em todo o tempo de análise. Portanto, nas condições de estudo estabelecidas, os sucos das empresas avaliadas foram citotóxicos, genotóxicos e mutagênicos. Estes resultados são importantes em razão de indicarem que tais alimentos têm relevante potencial em causar distúrbios celulares e, portanto, devem ser avaliados em sistemas com testes mais complexo, como os em roedores, para, dessa forma, estabelecer com propriedade a toxicidade em nível celular desses alimentos e assegurar o bem-estar daqueles que os consomem.

Effect of tumor necrosis factor-α on the proliferation and multi-directional differentiation of stem cells from rat apical papilla / 重庆医学

Objective To evaluate the biological effect of tumor necrosis factor-α(TNF-α) on the proliferation and multi-directional differentiation of stem cells from rat apical papilla(SCAP).Methods SCAP was extracted by combining enzyme digestion method with tissue block method.The cells were divided into control group(TNF-α 0 ng/mL) and experimental group(TNF-α 5,10,20,50 ng/mL).The ability of proliferation of SCAP was measured by MTT method.The ability of osteogenic/dentinogenic differentiation of SCAP was measured by alizarin red staining and quantitative real-time PCR.The ability of adipogenic of SCAP was measured by oil red O staining.The expression of vascular related genes of SCAP was measured by quantitative real-time PCR.Results SCAP was consistent with the characteristics of mesenchymal stem cells and possessed the ability of multi-directional differentiation.The MTT results showed that experimental group promoted the proliferation of SCAP in comparison with the control group.The difference was statistically significant(P<0.05),and 10 ng/mL was the optimum concentration.The results of alizarin red staining showed that with the increase of the concentration of TNF-α,the mineralized nodules in the experimental group gradually became smaller,and the number of the formation decreased gradually.The results of quantitative real-time PCR showed that the expression of OC,DMP-1 and DSPP in the experimental group was significantly lower than that of the control group at 3 and 7 days,in which the expression of OC was statistically significant different(P<0.05);at 14 days,the expression of OC,DMP-1 in the experimental group was significantly lower than that of the control group(P<0.05).The result of Oil red O staining showed that with the increase of the concentration of TNF-α,the lipid droplets formation in the experimental group gradually decreased.The result of quantitative real-time PCR showed that the expression of ANGPT1,VEGFA,PECAM-1 in the experimental group was significantly lower than that of the control group(P<0.05).Conclusion TNF-α might promote the proliferation and inhibit the multi-directional differentiation of SCAP.

Meristem culture and subsequent micropropagation of Chilean strawberry (Fragaria chiloensis (L) Duch. )

BACKGROUND: Vegetative propagation of Fragaria sp. is traditionally carried out using stolons. This system of propagation, in addition to being slow, can spread plant diseases, particularly serious being viral. In vitro culture of meristems and the establishment of micropropagation protocols are important tools for solving these problems. In recent years, considerable effort has been made to develop in vitro propagation of the commercial strawberry in order to produce virus-free plants of high quality. These previous results can serve as the basis for developing in vitro-based propagation technologies in the less studied species Fragaria chiloensis. RESULTS: In this context, we studied the cultivation of meristems and establishment of a micropropagation protocol for F. chiloensis. The addition of polyvinylpyrrolidone (PVP) improved the meristem regeneration efficiency of F. chiloensis accessions. Similarly, the use of 6-benzylaminopurine (BAP) in the culture media increased the average rate of multiplication to 3-6 shoots per plant. In addition, the use of 6-benzylaminopurine (BAP), had low levels (near zero) of explant losses due to oxidation. However, plant height as well as number of leaves and roots were higher in media without growth regulators, with average values of 0.5 cm, 9 leaves and 4 roots per plant. CONCLUSIONS: For the first time in Chilean strawberry, meristem culture demonstrated to be an efficient tool for eliminating virus from infected plants, giving the possibility to produce disease free propagation material. Also, the addition of PVP into the basal MS medium improved the efficiency of plant recovery from isolated meristems. Farmers can now access to high quality plant material produced by biotech tools which will improve their technological practices.

Obtención de semilla biotecnológica de caña de azúcar (Saccharum spp. híbrido) de alta calidad genética y fitosanitaria en el Ecuador / Obtainment of sugarcane (Saccharum spp. hybrid) biotechnological seed of high genetic and phytosanitary quality in Ecuador

Los métodos de saneamiento de plantas se basan fundamentalmente en el empleo combinado de cultivo in vitro de meristemos con tratamientos mediante hidrotermoterapia. Este trabajo se realizó con el objetivo de obtener plantas para usar como semilla libre de patógenos sistémicos, con énfasis en la enfermedad raquitismo de los retoños de la caña de azúcar (RSD). El trabajo se llevó a cabo con diferentes cultivares de caña de azúcar, los cuales fueron previamente identificados mediante marcadores bioquímicos basados en los patrones electroforéticos de isoenzimas peroxidasas. El saneamiento se realizó en tres etapas sucesivas mediante tratamiento hidrotérmico a 52 ºC durante 2h y uso del fungicida vitavax, un segundo tratamiento hidrotérmico a los meristemos a 51 ºC durante 10 min y una tercera etapa donde las vitroplántulas se propagaron en presencia del antibiótico gentamicina. La detección de RSD se efectuó mediante el empleo de la técnica de tinción de haces vasculares funcionales. Los resultados permitieron la creación de un banco de germoplasma de plantas libres de los principales patógenos bacterianos sistémicos y con alta calidad genética, lo que aportó semilla básica de excelente calidad para establecer semilleros. La conservación incluyó el mantenimiento de plántulas in vitro y la creación de un "banco de ADN" que permite conservar el genofondo en condiciones de laboratorio. Se propone finalmente una metodología para la obtención de plantas saneadas a partir de yemas y meristemos.

Methods for obtaining healthy plants are mainly based on the combined use of meristem in vitro culture and hydrothermotherapy. This work was carried out in order to obtain free- pathogen plants for using as seeds, emphasizing ratoon stunting disease (RSD) of sugarcane. The work was performed using a group of sugarcane cultivars, which was confirmed the variety identification by means of peroxidases isozymes electrophoretic patterns. Plant sanitation was performed in three successive steps by means of hydrothermal treatment at 52 ºC during 2h and using the fungicide vitavax, a second hydrothermal treatment at 51 °C during 10 min to the meristem and a third step in which vitroplantlets were propagated in presence of the antibiotic gentamicin. RSD detection was done by using the staining transpiration methods (STM) of functional bundles. Results allowed the creation of a germoplasm bank of sugarcane plants free of the most important systemic bacterial pathogens, with high genetic quality, which provided basic seed of excellent quality for establishing seedlings. Conservation included an in vitro-plantlets bank and the creation of a "DNA bank" which allows preserving the genetic fond in laboratory conditions. Finally a methodology for obtaining free-pathogens plants from buds and meristems is included.

Primary Somatic Embryos from Axillary Meristems and Immature Leaf Lobes of Selected African Cassava Varieties.

The study evaluated high-value African cassava varieties for primary somatic embryogenesis using axillary meristems (AM) and immature leaf lobes (LL) on piclorambased medium. The study was conducted at the Central Biotech Lab, International Institute of Tropical Agriculture (IITA), Ibadan, Nigeria between 2006 and 2009. Completely randomized design with four replicates was used for the study. Using LL explants, there were significant (P=.05) differences in percent responding leaf lobes, percent explant with pre-embryogenic structure, PSEF and PSEE among cassava varieties. The PSEF of the only three varieties that produced mature somatic embryo were 93.6, 88.5 and 85.7% for TME 12, Kibaha and Albert, respectively. Similarly, significant (P=.05) differences existed among the varieties in percent enlarged axillary meristem, percent explant with pre-embryogenic structure, PSEF and PSEE when AM was the explant. The PSEFs of the only three varieties that produced mature somatic embryo were 83.6, 77.5 and 72.7% for TME 12, Kibaha and Albert, respectively. The PSEF and PSEE of LL explant were greater than those of AM by an average of 86.1% and 82.7%, respectively. The study concluded that both AM and LL were good explants for production of primary somatic embryo in cassava.

Introducción y multiplicación in vitro del cultivo de ajo variedad Morado Barranquino

En este trabajo determinamos el efecto de medios de cultivo modificados usando diferentes concentraciones de reguladores de crecimiento (auxinas/citoquininas) para la regeneración y multiplicación in vitro del ajo (Allium sativum L.) variedad Morado Barranquino. En la fase de introducción se cultivó meristemos apicales en tubos de prueba hasta su regeneración y se determinó que el medio MSM + AIB 0,6 mg/L es el más adecuado para la diferenciación y desarrollo del meristemo. Para la multiplicación se utilizaron las microplantas (13 semanas) de la fase de introducción, obteniéndose formación de macollos en cada subcultivo; se logró mejor tasa de multiplicación en el medio MMA + AIA 2,5 mg/L + KIN 5 mg/L y el medio MSM + 2ip 1,5 mg/L con 4,71 y 4.79 respectivamente

We determine the effect of modified culture medium using different growth regulators concentrations (auxins / cytokinins) for regeneration and propagation of in vitro garlic plants (Allium sativum L.) var. ‘Morado Barrranquino. In the introduction stage meristem tips were cultured in test tubes up to regeneration. It was determined that medium MSM + IBA 0.6 mg/L was most suitable for the meristem tip differentiation and development. 13 weeks old microplants obtained on introduction stage were used for multiplication, obtaining the formation of a cluster after each subcultive. The best multiplication ratio was obtained in MMA medium + IAA 2.5 mg/L + KIN 5.0 mg/L and MSM medium + 2iP 1.5 mg/L with 4.71 and 4.79 respectively

Elimination of TSWV from impatiens hawkerii Bull. and regeneration of virus-free plant

The possibility for obtaining virus free plants from Impatiens hawkerii Bull. shoots infected with Tomato spotted wilt virus (TSWV) through meristem-tip culture was examined. TSWV presence in I. hawkerii plants was detected by DAS-ELISA and RT-PCR and identification of the virus was confirmed by sequencing one of the chosen isolate (GenBank Accesion CQ132190). Meristem-tip explants (0.3-1.5 mm) from virus-infected shoots are cultured on MS media supplemented with different concentrations of the cytokinins, CPPU or TDZ (0.01-1.0 uM), respectively. Using this system, a large number of in vitro shoots could be produced from a single explant. Also, cytokinins showed a stimulatory effect on the length, fresh and dry weights of the newly formed shoots. Plant pigments content in I. hawkerii shoots increased significantly in the presence of cytokinins. Rooting of shoots was spontaneous on the same media. Rooted plantlets were transferred to soil where 97 percent successfully acclimatized. By DAS-ELISA and RT-PCR, 80 percent of the in vitro plantlets were shown to be a virus-free. Considering these, the present protocol seems to be an efficient method for in vitro generation of virus-free I. hawkerii plantlets by meristem tip cultures.

Avaliação do potencial citotóxico dos chás de Camellia sinensis L. e Cassia angustifolia vahl em sistema teste vegetal / Cytotoxic potencial evaluation from the Camellia sinensis and Cassia angustifolia vahl teas, in vegetal test system

Os chás de Camellia sinensis (chá verde) e Cassia angustifolia (chá sene) são amplamente consumidos pela população brasileira, em função de suas propriedades antioxidantes e laxativas, respectivamente. Neste trabalho, foi avaliada a citotoxicidade do chá de Camellia sinensis e do chá de Cassia angustifolia, dos quais se obteve três amostras (soluções-tratamento) para cada chá: chá verde - 0,57; 1,15 e 2,30%m/V e chá sene - 0,85; 1,70 e 3,40%m/V. Para esta avaliação, utilizou-se as células meristemáticas de raiz de Allium cepa L. e estabeleceram-se 3 grupos: CO (0h), TR (24h) e RE (24h). Foram analisadas 5.000 células por grupo, para o cálculo do índice mitótico médio de cada grupo e a análise estatística foi feita pelo teste do Qui-quadrado. A partir dos resultados obtidos, verificou-se que as amostras testadas dos chás das duas plantas não causaram ação citotóxica, estatisticamente significativa, e nem alterações cromossômicas no sistema teste utilizado.

The Camellia sinensis (green tea) and Cassia angustifolia (sene tea) teas are very consumed by the Brazilian population for its antioxidants and laxative properties, respectively. In this work it was evaluated the Camellia sinensis tea and Cassia angustifólia cytotocity, where it was obtained three samples (treatment-solutions) for each tea: green tea - 0,57; 1,15 e 2,30%m/V e sene tea - 0,85; 1,70 e 3,40%m/V. For this evaluation it was used the embryonic tissue from the Allium cepa roots and it was established three groups: CO (0h), TR (24h) and RE (24h). 5.000 cells were analyzed in each group and the statistic was made by the Qui-square test. As of the obtained results, it was verified that the both plants tested samples tea didn?t cause cytotoxic action, statistically significant, not even chromosome alterations, in the used test system.

Ação do BAP na regeneração in vitro de Blc Owen Holmes Ponkan x Brassavola digbiana nº 2 / BAP (6-benzylaminopurine) in the regeneration in vitro of Blc Owen Holmes Ponkan x Brassavola digbiana nº 2

A Cattleya é considerada a mais bela e procurada de todas as orquídeas. Esta demanda cria a necessidade do desenvolvimento de técnicas mais eficazes de propagação que ofereçam maior número de indivíduos em período de tempo e espaço físico reduzido, além de manterem a uniformidade e a identidade genotípica para atender às exigências do mercado. Objetivou-se neste trabalho avaliar a regeneração de meristemas provenientes de gemas cultivadas in vitro do híbrido Blc Owen Holmes Ponkan x Brassavola digbiana nº 2, em diferentes concentrações de BAP (6-benzilaminopurina). Gemas com 37 dias de cultivo foram inoculadas em meio de cultura líquido com reguladores vegetais, nos respectivos tratamentos: T1 - MS líquido + água de coco; T2 - MS + água de coco + 0,1 mg L-1 ANA (ácido naftaleno acético) + 0,2 mg L-1 BAP; T3 - MS + água de coco + 0,1 mg L-1 ANA + 0,5 mg L-1 BAP; T4 - MS + água de coco + 0,1 mg L-1 ANA + 1,0 mg L-1 BAP. Os subcultivos se realizaram aos 18, 32, 62, 93, 123, 153 e 184 dias e as avaliações foram feitas observando-se a porcentagem de sobrevivência, contaminação, oxidação e regeneração dos explantes. Observou-se que 86,7 por cento dos explantes sobreviveram e aos 93 dias ocorreu o primeiro sinal de regeneração. BAP (1,0 mg L-1) promoveu resultados satisfatórios com a formação de 132 perfilhos aos 184 dias de cultivo, potencializando a técnica para produção em escala comercial dessa espécie.

Cattleya is considered the most beautiful and searched among all orchids. This fact creates the need of developing more effective propagation techniques to become available a greater number of individuals in reduced periods of time and physical space, besides maintenance of uniformity and genotipic identity to meet the needs of the market. The objective of this work was to evaluate the regeneration of the cultivated shoot meristematic in vitro of the hybrid Blc Owen Holmes Ponkan x Brassavola digbiana nº 2 in the different BAP (6-benzylaminopurine) concentrations. The explants were inoculated in the liquid medium with or without growth regulators in the following combinations: T1: MS liquid + coconut water; T2: MS + coconut water + 0.1 mg L-1 NAA + 0.2 mg L-1 BAP; T3: MS + coconut water + 0.1 mg L-1 NAA + 0.5 mg L-1 BAP and T4: MS + coconut water + 0.1 mg L-1 NAA + 1.0 mg L-1 BAP. Subcultivatings and evaluations (percentage of survival, contamination, medium color, oxidation and regeneration) were made at 18, 32, 62, 93, 123, 153, and 184 days. At 93 days the first signs of regeneration were observed. BAP (1.0 mg L-1) enhanced good results with the formation of 132 sprouts in the 184 days, concluded that the utilization of BAP improved morphogenic response with a higher number of shoots.

Plant tissue culture techniques

Plant cell and tissue culture in a simple fashion refers to techniques which utilize either single plant cells, groups of unorganized cells (callus) or organized tissues or organs put in culture, under controlled sterile conditions.