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Relevant bibliographies by topics / Tomatoes Plant tissue culture

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Academic literature on the topic 'Tomatoes Plant tissue culture'

Author: Grafiati

Published: 4 June 2021

Last updated: 14 February 2022

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Journal articles on the topic "Tomatoes Plant tissue culture"

1

Davis, Jeanine M., Douglas C. Sanders, Paul V. Nelson, Laura Lengnick, and Wade J. Sperry. "Boron Improves Growth, Yield, Quality, and Nutrient Content of Tomato." Journal of the American Society for Horticultural Science 128, no. 3 (May 2003): 441–46. http://dx.doi.org/10.21273/jashs.128.3.0441.

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Boron deficiency in fresh-market tomatoes (Lycopersicon esculentum Mill.) is a widespread problem that reduces yield and fruit quality but is often not recognized by growers. Tomatoes were grown in field and hydroponic culture to compare the effects of foliar and soil applied B on plant growth, fruit yield, fruit quality, and tissue nutrient levels. Regardless of application method, B was associated with increased tomato growth and the concentration of K, Ca, and B in plant tissue. Boron application was associated with increased N uptake by tomato in field culture, but not under hydroponic culture. In field culture, foliar and/or soil applied B similarly increased fresh-market tomato plant and root dry weight, uptake, and tissue concentrations of N, Ca, K, and B, and improved fruit set, total yields, marketable yields, fruit shelf life, and fruit firmness. The similar growth and yield responses of tomato to foliar and root B application suggests that B is translocated in the phloem in tomatoes. Fruit from plants receiving foliar or root applied B contained more B, and K than fruit from plants not receiving B, indicating that B was translocated from leaves to fruit and is an important factor in the management of K nutrition in tomato.

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Sharma, V. K., and J. Nowak. "Enhancement of verticillium wilt resistance in tomato transplants by in vitro co-culture of seedlings with a plant growth promoting rhizobacterium (Pseudomonas sp. strain PsJN)." Canadian Journal of Microbiology 44, no. 6 (June 1, 1998): 528–36. http://dx.doi.org/10.1139/w98-017.

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The potential utilization of a plant growth promoting rhizobacterium, Pseudomonas sp. strain PsJN, to enhance the resistance of tomato transplants to verticillium wilt was investigated. Plant growth and disease development were tested on the disease-susceptible cultivar Bonny Best after Verticillium dahliae infection of tissue culture plantlets bacterized in vitro (by co-culturing with the bacterium) and seedlings bacterized in vivo (after 3 weeks growth in the greenhouse). Significant differences in both disease suppression and plant growth were obtained between in vitro bacterized and nonbacterized (control) plants. The degree of protection afforded by in vitro bacterization depended on the inoculum density of V. dahliae; the best and worst protection occurred at the lowest (103 conidia ·mL-1) and highest (106 conidia ·mL-1) levels, respectively. In contrast, the in vivo bacterized tomatoes did not show plant growth promotion when compared to the nonbacterized control plants. When challenged with Verticillium, significant growth differences between in vivo bacterized plants (26.8% for shoot height) and nonbacterized controls were only seen at the 3rd week after inoculation. Compared with the in vitro inoculation, there was no delay in the verticillium wilt symptom expression, even at the lowest concentration of V. dahliae, by in vivo PsJN inoculation. These results suggest that endophytic colonization of tomato tissues is required for the Verticillium-resistance responses. Plant growth promotion preceeds the disease-resistance responses and may depend on the colonization thresholds and subsequent sensitization of hosts.Key words: Pseudomonas sp., plant growth promoting rhizobacterium, Verticillium dahliae, tomato, colonization, plant growth promotion, disease suppression.

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Ikeda, Takashi, Kunio Okano, Yuka Sakamoto, and Shin-ichi Watanabe. "275 Water Relations of Fruit Cracking in Single-truss Tomato Plants." HortScience 34, no. 3 (June 1999): 489E—489. http://dx.doi.org/10.21273/hortsci.34.3.489e.

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This study was undertaken to investigate the water relations of tomato (Lycopersicon esculentum Mill.) fruit cracking for single-truss tomato plants. The tomato plants were cultured on a closed hydroponic system in greenhouse. Water status of culture solution and plant tissues was measured with psychrometers. Water potential of the culture solution for the stressed plant was changed from -0.06 MPa (control plants) to -0.36 MPa at 24 days after anthesis. Hardness of the fruit skin was not different significantly between the stressed plants and the control plants. Fruit cracking occurred frequently in the control plants, but not in the stressed plants. Water potential gradient between the tissue of fruit flesh and water source for the control plants was bigger than that of the stressed plants. Turgors were increased at the tissues of fruit flesh and fruit skin at the control plants between predawn and morning but not at the stressed plants. These results indicated that the water potential gradient and the increased turgor in these tissues might be a trigger for the occurrence of fruit cracking on single-truss tomato plants.

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Rao, Gonella S. R. L., J. H. Martin Willison, and W. M. Nimal Ratnayake. "Suberization of tomato (Lycopersicon esculentum) locule tissue." Canadian Journal of Botany 63, no. 12 (December 1, 1985): 2177–80. http://dx.doi.org/10.1139/b85-308.

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It was demonstrated by electron microscopy that wounded and cultured tomato fruit outer placental (locule) tissue generated lamellated (secondary) walls. BF3 – methanol depolymerization of an extract from these walls and its chromatographic analysis showed the presence of the polymer suberin in the tissue adjacent to the wound after 7 days in culture. Quantitative studies using Iatroscan thin-layer chromatography coupled with flame ionization detection showed close similarities between the aliphatics of this wound suberin (which constituted 70% of the total monomers recovered) and that generated by protoplasts isolated from the same tissue, particularly among the monofunctional products, but some striking differences among the difunctional products. It is proposed that the results support the concept that protoplast isolation elicits a wound response similar to that elicited by mechanical wounding of the mother tissue, but that the physiological conditions obtained during protoplast isolation and culture result in a modification of this response.

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Greer, Ann Francine, and Zohreh Tabaeizadeh. "Characterization and plant regeneration of cell suspension cultures of Lycopersicon chilense." Canadian Journal of Botany 69, no. 10 (October 1, 1991): 2257–60. http://dx.doi.org/10.1139/b91-283.

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To produce calli for the establishment of a cell suspension, leaf, stem, and petiole explants of Lycopersicon chilense Dun., grown in vitro and in the soil, were cultured on media containing 15 different combinations of benzylaminopurine, kinetin, and indole acetic acid. Among the three types of tissues, leaf explants showed the best response. Cell suspension cultures of L. chilense were established from leaf callus derived from soil grown plants using Murashige and Skoog's medium supplemented with casein hydrolysate (250 mg/L), coconut water (5%), and 2,4-dichlorophenoxyacetic acid (2 mg/L). Once established, cell suspensions showed a rapid growth rate with no marked lag phase. Shooting via organogenesis occurred from callus derived from cell suspensions on medium containing 2 mg/L benzylaminopurine. Regenerated plants had the same morphology as the original plants. Key words: Lycopersicon chilense, tomato, tissue culture, cell suspensions, organogenesis, plant regeneration.

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Sanjaya, I. Putu Wahyu, Rindang Dwiyani, I. Gede Putu Wirawan, and Bambang Sugiharto. "PRICK AND SOAK Agroacterium tumefaciens-MEDIATED IN PLANTA TRANSFORMATION IN TOMATO (Lycopersicon esculentum Mill.)." International Journal of Biosciences and Biotechnology 5, no. 2 (May 21, 2018): 124. http://dx.doi.org/10.24843/ijbb.2018.v05.i02.p05.

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One of the modern plant breedings through genetic engineering is Agrobacterium tumefaciens-mediated transformation. Agrobacterium tumefaciens-mediated transformation can be performed in vitro or in planta. In planta transformation arises from the weaknesses of the in vitro method such as need high hygiene standard, professional tissue culture experts, and more time to prepare explants and somaclonal variation. In planta transformation is a method to transfer the gene to the plant genome without any tissue culture stages. The aims of this research were to know the possibility of the prick and soak in planta method with the target of tomato seeds and to know the most suitable inoculation time for tomato seeds transformation by prick and soak method the transformation is done by pricking the seeds and soaking them in the A. tumefaciens suspension. The treatments in this study were 1 and 2 days inoculation time to test the efficacy of prick and soak in planta transformation method. Tomato seeds were pricked with a needle on the center once, and then soaked in A. tumefaciens strain LB4404 suspension carrying pKYS-SoSPS1 plasmid with Neomycin Phosphotransferase (NPTII) and Saccharum officinarum Sucrose Phosphate synthase (SoSPS1) genes. Visualization of tomato’s DNA samples after PCR showed that 1-day inoculation sample was positively integrated with NPTII gene and negative in the 2 days inoculation treatment.

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Maas, John L., Gene J. Galletta, and Barbara J. Smith. "529 PB 525 DETERMINING RESISTANCE IN STRAWBERRY TO ANTHRACNOSE USING TOXINS PRODUCED IN FUNGUS CULTURE." HortScience 29, no. 5 (May 1994): 507b—507. http://dx.doi.org/10.21273/hortsci.29.5.507b.

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We have determined in tests conducted both at Beltsville and Poplarville that several strawberry isolates of Colletotrichum acutatum, C. gloeosporioides and C. fragariae produce toxin-like compounds in culture. Crude culture filtrates (CFI elicited general and specific responses in tomato and strawberry plants. Tomato plants initially were used because they are highly responsive to toxins in general, whereas the reaction of strawberry plants apparently is greatly affected by environmental and nutritional growing conditions of the test plant. Toxin symptoms included leaf chlorosis and wilting, leaf midvein darkening, and plant death when CF was applied to leaves or if seedlings or petioles were immersed into CF. Juvenile tissues appear to be more susceptible to the effects of the toxins than mature tissue. No differences in response to culture filtrates were apparent among those from the Colletotrichum isolates. The putative toxins appear to act differentially with susceptible or resistant strawberry germplasm.

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Ajenifujah-Solebo, Shakirat Oloruntoyin, Isu N. A., Olorode O., and Ingelbrecht I. "Effect of Cultivar and Explants Type on Tissue Culture Regeneration of Three Nigerian Cultivars of Tomatoes." Sustainable Agriculture Research 2, no. 3 (May 2, 2013): 58. http://dx.doi.org/10.5539/sar.v2n3p58.

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<p>In order to assess the suitable explant(s) for <em>in-vitro</em> regeneration of three local cultivars of Nigerian tomatoes, Ibadan local (IbL), Ife and JM94/46, cotyledon, hypocotyls and radicle explants were cultured in shoot regeneration medium consisting of<strong> </strong>MS containing 30 g L<sup>-1</sup> sucrose and 8 g L<sup>-1 </sup>agar with no exogenous plant growth hormones. Forty-five of each explant type was cultured on the medium in triplicate experiments and results showed varied percentage survival and shooting for the various explants. Hypocotyl explants had the highest percentage of shooting explants at 13.3% for IbL; 6.67% for Ife and 20% in JM94/46. IbL cotyledon explants had 4.44% of shooting explants with no shoots recorded in Ife and JM94/46 cotyledon explants. IbL radicle explants had 2.22% shooting explants and no shoots recorded in Ife and JM94/46. Student Neuman Keuls (SNK) statistical analysis of cultivar-media interaction showed there was no significant difference (P > 0.05) among the three cultivars in number of calli and shooting calli. There was however significant difference among the cultivars in the number of shoots recorded. SNK values for explants-media interaction showed that cotyledon and radicle explants were significantly different (P < 0.05) from hypocotyl explants in the number of shoots produced.</p>

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Hanus-Fajerska, Ewa. "Studies on the reaction in tissue culture of tomato genotypes under biotic stress." Acta Societatis Botanicorum Poloniae 70, no. 1 (2014): 5–10. http://dx.doi.org/10.5586/asbp.2001.001.

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Plant regeneration in vitro from virus-infected somatic tomato (<em>Lycopersicon</em> sp.) tissue was performed. Regeneration experiments were started after the determination of virus presence, using enzyme-linked immunosorbent assay, in leaves used as a source of explants. Leaf explants infected with selected strains of tomato mosaic <em>Tobamovirus</em> or cucumber mosaic <em>Cucumovirus</em> respectively, were cultured on a standarised MS agar medium to induce adventitious shoots, which were afterwards excised, rooted in vitro and cultured to plants. Explants were also screened for their ability to produce callus. Diverse effects of viral infection, ranging from stimulation to inhibition of callus formation and of morphogenesis rate, were observed. The health condition of the tissue proved to affect regeneration potential of <em>Lycopersicon esculentum</em>, whereas wild accesions did not react in that case so distinctly. In cultivated tomato was encountered the decline in competence to reproduce shoots adventitiously in infected tissue. There was also relationship between donor plant health condition and adventitious root formation in regenerated shoots. Experiments with short-term cultures of <em>L. esculenum</em> reveled also that a certain number of shoots regenerated from diseased tissue can be virus-free.

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Lech, M., K. Miczyński, and A. Pindel. "Comparison of regeneration potentials in tissue cultures of primitive and cultivated tomato species (Lycopersicon sp.)." Acta Societatis Botanicorum Poloniae 65, no. 1-2 (2014): 53–56. http://dx.doi.org/10.5586/asbp.1996.009.

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Regeneration capacities of two tomato cultivars: Potentat and Rutgers, and of three accessions of wild tomato species: <em>Lycopersicon peruvianum</em> PI 128650, <em>L. peruvianum var. dentatum</em> PI 128655 and <em>L. glandulosum</em> were studied using an universal medium suitable for regeneration of those plants from leaf pieces in tissue culture. Fragments of leaf blades were taken from plants raised in greenhouse conditions and placed on a modified MS medium containing 0.3 mg/l IAA and 3.0 mg/l BAP solidified with 1% agar. The explants were transferred every 4-5 weeks on fresh medium of the same composition. It was shown that all the three primitive tomato species revealed much higher multiplication coefficients than the two cultivars. Appropriate values were: 11 - for <em>L. glandulosum</em>, 8 - for <em>L. peruvianum</em>, 7 - for <em>L. peruvianum var. dentatum</em>, 4 - for <em>L. esculentum</em> cv. Potentat and 2 - cv. Rutgers. Completely regenerated plants were obtained from all the tested species, but organogenesis occurred almost two weeks earlier in wild tomatoes than in the culitivated varieties of <em>L. esculentum</em>.

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Dissertations / Theses on the topic "Tomatoes Plant tissue culture"

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Compton, Michael E. "De novo morphogenesis on tomato thin cell layers and variation for genetic recombination among plantlets regenerated from tissue culture." Diss., This resource online, 1990. http://scholar.lib.vt.edu/theses/available/etd-09162005-115005/.

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Carvalho, Rogério Falleiros. "Uso de mutantes fotomorfogenéticos no estudo da competência para regeneração in vitro em micro-tomateiro (Lycopersicon esculentum CV Micro-Tom." Universidade de São Paulo, 2004. http://www.teses.usp.br/teses/disponiveis/11/11144/tde-19022004-103113/.

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Paralelamente ao modelo Arabidopsis thaliana, o tomateiro (Lycopersicon esculentum) tem sido crescentemente utilizados em abordagens genéticas de questões fisiológicas. Uma das principais vantagens de Arabidopsis como planta de laboratório tem sido seu pequeno porte e ciclo de vida curto. Contudo, a cultivar Micro-Tom (MT) de tomateiro possui tamanho muito reduzido (8 cm) e pode produzir até 5 gerações por ano. Mutantes fotomorfogenéticos em tomateiro deficientes na síntese do cromóforo do fitocromo (au), mutantes deficientes na síntese das apoproteínas PHYA e PHYB1 (fri e tri, respectivamente) e mutantes superexpressando o fitocromo (hp, atv e Ip) constituem-se em um modelo para estudos da fotomorfogênese. No que se refere à capacidade de regeneração in vitro como uma resposta fotomorfogenética, poucos trabalhos têm sido realizados. O presente trabalho teve como objetivo transferir as mutações au, fri, tri, hp, Ip e atv, bem como o locus de regeneração (Rg1) da cultivar MsK, para a cultivar Micro-Tom. As linhagens obtidas foram utilizadas para verificar o efeito da fotomorfogênese na competência para regeneração in vitro. Para tanto, foram realizados tratamentos com luz branca, vermelho (V) e vermelho-extremo (VE) em explantes radiculares, caulinares e foliares do genótipo micro-MsK em meio MS mais 5mM de BAP e tratamentos com luz branca em explantes radiculares, caulinares e foliares de micro-mutantes fotomorfogenéticos também em meio MS mais 5mM de BAP. Para todos os tratamentos utilizou-se a cultivar MT como controle. Sob V, as raízes de micro-MsK apresentaram-se diferenciadas, enquanto sob VE não ocorreu diferenciação. O maior número de gemas formadas tanto para caule quanto para folhas de micro-MsK ocorreu sob V, enquanto sob VE foi observado um decréscimo na formação de gemas. A partir destes resultados sugere-se que a forma ativa do fitocromo, induzida pelo V, interage com o Rg1 na aquisição de competência para regeneração. Nos tratamentos com luz branca, raízes de micro-MsK e de mutantes micro-hp, micro-atv e micro-Ip apresentaram-se diferenciadas, enquanto não houve diferenciação para o mutante micro-au ou para o controle MT. O número de gemas formadas alcançou maiores valores para folhas de micro-hp e micro-Ip e a para caules de micro-atv. Apenas um número muito reduzido de gemas foi formado a partir de folhas de micro-au. Com base na alta competência para regeneração de micro-MsK e de mutantes que superexpressam o fitocromo, sugere-se que o fitocromo promove, em uma via de sinalização, a indução de fatores de regeneração (Rg1). Alternativamente, o locus Rg1 poderia promover a alta capacidade regenerativa tornando os explantes mais competentes ao efeito da superexpressão do fitocromo, o qual poderia induzir outros fatores de regeneração.
Parallel to Arabidopsis thaliana model, the tomato (Lycopersicon esculentum) has been increasingly used as a genetic approach to address physiological questions. One of the main advantages of Arabidopsis as a laboratory plant has been its small size and short life cycle. However, the tomato cultivar Micro-Tom (MT) possesses reduced size (8 cm) and can produce up to 5 generations per year. Tomato photomorphogenic mutants deficient for the synthesis of phytochrome chromophore (au) or the apoprotein PHYA and PHYB1 (fri and tri, respectively), as well as mutants superexpressing phytochrome (hp, atv and Ip) consist on a model to study photomorphogenesis. Concerning the in vitro regeneration capacity as a photomorphogenic response, fewer works have been carried through. The current work aimed at transfering the mutations au, fri, tri, hp, Ip and atv, as well as the regeneration locus (Rg1) of cv MsK to the cv Micro-Tom (MT). The genotypes obtained were used to verify the effect of photomorphogenesis on the competence for in vitro regeneration. Root, stem and leaf explants from MT and Micro-MsK were incubated in MS plus 5mM BAP under white, red (R) and far-red (FR) light. Root, stem and leaf explants from MT and photomorphogenic micro-mutants were incubated in MS plus 5mM BAP under white light. Under R, roots of micro-MsK were presented differentiation, while under FR the differentiation did not occur. Under R, stem explants from micro-MsK formed more shoots than did leaf explants, while under FR was observed a decrease in shoot formation for all types of explants. These results suggest that the active form of phytochrome, induced by R, interacts with the Rg1 in the acquisition of competence for regeneration. In the treatments with white light, roots of micro-MsK and of mutants micro-hp, micro-atv and micro-Ip presented differentiation, while no differentiation was observed for the mutant micron-au or control MT. The number of shoots formed reached the highest values for leaf explants of micro-hp and micro-Ip and for stem explants of micron -atv. Only a low number of shoots was formed from micro-au leaf explants. On the basis of the high competence for regeneration of micro-MsK and mutants that super express phytochrome, it is suggested that the phytochrome promotes, in a signaling pathway, the induction of regeneration factors ( Rg1 ). Alternatively, the Rg1 locus may turn the explant most competent to respond to phytochrome, which could induces others regeneration factors.

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Slomka, Marek Jozef. "Studies of tomato golden mosaic virus in plants, protoplasts and tissue culture." Thesis, Imperial College London, 1987. http://hdl.handle.net/10044/1/46616.

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Sheibani, Ahmad. "Tissue culture studies of Pistacia." Thesis, University of Salford, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.238801.

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Al-Ani, Nabeel K. "Some epigenetic effects in plant tissue culture." Thesis, Aberystwyth University, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.659362.

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VanTine, Melissa C. "Effect of watering regime and media components on the production of organic tomato transplants." Morgantown, W. Va. : [West Virginia University Libraries], 2004. https://etd.wvu.edu/etd/controller.jsp?moduleName=documentdata&jsp%5FetdId=3619.

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Thesis (M.S.)--West Virginia University, 2004.
Title from document title page. Document formatted into pages; contains vii, 60 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 56-60).

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James, V. J. "Regulation of xenobiotic catabolism in plant tissue culture." Thesis, Cardiff University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.380205.

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Wardrop, Julie. "Biotechnological applications of perfluorochemical liquids in plant tissue culture." Thesis, University of Nottingham, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.389475.

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Al, Kaabi Helel Humaid Saed Humaid. "Date palm tissue culture and AFLP analysis of plant variability." Thesis, Imperial College London, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.409314.

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Ghadimzadeh, Mortaza. "Studies of protoplast and liposome techniques in plant tissue culture." Thesis, University of Salford, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.255239.

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Books on the topic "Tomatoes Plant tissue culture"

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Laimer, Margit, and Waltraud Rücker, eds. Plant Tissue Culture. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4.

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Kumar, Sandeep. Plant tissue culture. Jabalpur: Tropical Forest Research Institute, 1997.

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Trivedi, Pravin Chandra. Plant tissue culture & biotechnology. Jaipur: Pointer Publishers, 2006.

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Lindsey, K., ed. Plant Tissue Culture Manual. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0181-0.

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Lindsey, K., ed. Plant Tissue Culture Manual. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0303-9.

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Dutta Gupta, S., and Yasuomi Ibaraki, eds. Plant Tissue Culture Engineering. Berlin/Heidelberg: Springer-Verlag, 2006. http://dx.doi.org/10.1007/1-4020-3694-9.

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Lindsey, K., ed. Plant Tissue Culture Manual. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4899-3776-6.

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Lindsey, K., ed. Plant Tissue Culture Manual. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4899-3778-0.

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Lindsey, K., ed. Plant Tissue Culture Manual. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-009-0103-2.

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E, Vidaver William, ed. Glossary of plant tissue culture. Portland, Or: Dioscorides Press, 1988.

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Book chapters on the topic "Tomatoes Plant tissue culture"

1

McCormick, Sheila. "Transformation of tomato with Agrobacterium tumefaciens." In Plant Tissue Culture Manual, 311–19. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-009-0103-2_17.

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Loyola-Vargas, Víctor M., C. De-la-Peña, R. M. Galaz-Ávalos, and F. R. Quiroz-Figueroa. "Plant Tissue Culture." In Springer Protocols Handbooks, 875–904. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-375-6_50.

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Priyadarshan, P. M. "Tissue Culture." In PLANT BREEDING: Classical to Modern, 475–91. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7095-3_21.

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Haberlandt, G. "Culturversuche mit isolierten Pflanzenzellen." In Plant Tissue Culture, 1–24. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4_1.

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Lucca, Paolo, and Ingo Potrykus. "Genetic engineering technology against malnutrition." In Plant Tissue Culture, 167–74. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4_10.

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Zoglauer, Kurt, U. Behrendt, A. Rahmat, H. Ross, and Taryono. "Somatic embryogenesis — the gate to biotechnology in conifers." In Plant Tissue Culture, 175–202. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4_11.

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Wilhelm, Eva. "Tissue culture of broad-leafed forest tree species." In Plant Tissue Culture, 203–16. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4_12.

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Laimer, M. "The development of transformation of temperate woody fruit crops." In Plant Tissue Culture, 217–42. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4_13.

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Krikorian, A. D., and David L. Berquam. "Plant Cell and Tissue Cultures: The Role of Haberlandt." In Plant Tissue Culture, 25–53. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4_2.

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Härtel, O. "Gottlieb Haberlandt (1854-1945): a portrait." In Plant Tissue Culture, 55–66. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4_3.

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Conference papers on the topic "Tomatoes Plant tissue culture"

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"Stress-inducible and tissue-specific promoters in transgenic tomatoes." In Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, 2019. http://dx.doi.org/10.18699/plantgen2019-180.

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Suberliak, Sofia. "Method of tissue culture for biodiversity conservation of medical plants of Carpatians." In ASPB PLANT BIOLOGY 2020. USA: ASPB, 2020. http://dx.doi.org/10.46678/pb.20.1048274.

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Vazquez Rueda, Martin G., Federico Hahn, and Jose L. Zapata. "Adaptive image segmentation applied to plant reproduction by tissue culture." In AeroSense '97, edited by Steven K. Rogers. SPIE, 1997. http://dx.doi.org/10.1117/12.271476.

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Yang, Yanli, Qi Chu, Meizhang Gu, Hanhan Ji, and Song Gu. "Simulation analysis and experiment of unpowered roller conveying for culture bottle in tissue culture plant." In 2021 6th International Conference on Automation, Control and Robotics Engineering (CACRE). IEEE, 2021. http://dx.doi.org/10.1109/cacre52464.2021.9501338.

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"Alterations of differential gene expression during the morphogenesis induction in wheat tissue culture (transcriptome analysis)." In Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, 2019. http://dx.doi.org/10.18699/plantgen2019-029.

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Seelye, Jared T., Gourab Sen Gupta, and John Seelye. "Investigations into a low-cost TDS sensor for sterile plant tissue culture media." In 2017 IEEE International Instrumentation and Measurement Technology Conference (I2MTC). IEEE, 2017. http://dx.doi.org/10.1109/i2mtc.2017.7969839.

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Zhou, Hong, Xiating Yu, and Junlin Yu. "Non-destructive growth measurement of tissue-culture orchid plant based on machine vision." In 2011 International Conference on Electrical and Control Engineering (ICECE). IEEE, 2011. http://dx.doi.org/10.1109/iceceng.2011.6057913.

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Vazquez Rueda, Martin G., and Federico Hahn. "Pattern matching and adaptive image segmentation applied to plant reproduction by tissue culture." In AeroSense '99, edited by Kevin L. Priddy, Paul E. Keller, David B. Fogel, and James C. Bezdek. SPIE, 1999. http://dx.doi.org/10.1117/12.342894.

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adil, Muhammad. "Production of high valued medicinal compounds using plant cell tissue and organ culture." In 5th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2019. http://dx.doi.org/10.3390/ecmc2019-06308.

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Echeverri Del Sarto, Julieta, María Celeste Gallia, Ana Ferrari, and Guillermina A. Bongiovanni. "TISSUE PLANT CULTURE AS A NOVEL INDUSTRIAL STRATEGY TO PRODUCE BIOPHARMACEUTICALS FROM ENDANGERED PLANTS." In 24th International Academic Conference, Barcelona. International Institute of Social and Economic Sciences, 2016. http://dx.doi.org/10.20472/iac.2016.024.030.

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Reports on the topic "Tomatoes Plant tissue culture"

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Scott, C. D., and D. K. Dougall. Plant cell tissue culture: A potential source of chemicals. Office of Scientific and Technical Information (OSTI), August 1987. http://dx.doi.org/10.2172/5938126.

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