http://pccm.ufla.br/index.php/plantcellculturemicropropagation/issue/feed Plant Cell Culture & Micropropagation - ISSN 1808-9909 2023-03-30T20:52:30-03:00 Plant Cell Culture & Micropropagation plantcellcm@gmail.com Open Journal Systems <p><strong>Plant Cell Culture &amp; Micropropagation</strong> is a journal that publishes scientific papers in the area of plant tissue culture and applied plant biotechnology, including micropropagation; genetic transformation; plant regeneration; organogenesis, and somatic embryogenesis, morphogenesis; functional genomics and metabolic engineering.</p><p><span>Submitted manuscripts must be written in English, be original, and be in accordance with the journal's standards and not be submitted for publication elsewhere. Its content (data, ideas, opinions, and concepts) is the sole responsibility of the author(s). </span></p><p><strong><span style="font-size: 1.17em;"><br /></span></strong></p><p><strong><span style="font-size: 1.17em;">ONLINE SUBMISSIONS</span></strong></p><p>Already have a Username/Password for Plant Cell Culture &amp; Micropropagation?<br /><a class="action" href="/ojs/index.php/PlantCellCultureMicropropagation/login">GO TO LOGIN</a></p><p>Need a Username/Password?<br /><a class="action" href="/ojs/index.php/PlantCellCultureMicropropagation/user/register">GO TO REGISTRATION</a></p><p>Registration and login are required to submit items online and to check the status of current submissions.</p><p><span><br /></span></p><p><span style="font-size: 1.17em;"><strong>AUTHOR GUIDELINES</strong> (<a href="/ojs/index.php/PlantCellCultureMicropropagation/about/submissions#authorGuidelines">http://177.105.2.193/ojs/index.php/PlantCellCultureMicropropagation/about/submissions#authorGuidelines</a>)</span></p><p> </p><p> </p><p><strong>INFORMATION</strong></p><p><strong>PREZADOS USUÁRIOS AO SE CADASTRAREM NO SISTEMA VERIFIQUEM SE TODOS OS DADOS FORAM PREENCHIDOS E NA OPÇÃO URL ADICIONEM O LINK PARA O CURRÍCULO LATTES. </strong></p><p><strong>É IMPORTANTE QUE TANTO OS AUTORES COMO OS CO-AUTORES SE CADASTREM NO SISTEMA NO MOMENTO DA SUBMISSÃO DE ARTIGOS.</strong></p> http://pccm.ufla.br/index.php/plantcellculturemicropropagation/article/view/190 Establishment and clonal propagation of Lippia dulcis Trevir. through in vitro single node cultures 2023-01-26T15:00:30-03:00 Taina Teixeira Rocha tainarocha@yahoo.com.br Diene Xavier Araújo diennearaujo@yahoo.com.br Rafael Marlon Alves de Assis rafamarlon7@gmail.com Alexandre Alves de Carvalho alexandre.ufla@yahoo.com.br Suzan Kelly Vilela Bertolucci suzan@ufla.br José Eduardo Brasil Pereira Pinto jeduardo@ufla.br <p>Lippia dulcis Trevir. (Verbenaceae) is a species with medicinal potential that is used as a tranquilizer and to control diabetes in the western region of Pará, Brazil. The objective of this study was to determine the establishment and clonal propagation of Lippia dulcis through single nodal segments grown in different concentrations of salts in a MS (Murashige and Skoog) medium (MS, MS/2, MS/4) and determine the best period for subculturing the species. Nodal segments cultivated in the MS medium showed a higher survival percentage and better development than those grown in more dilute media (MS/2, MS/4). The concentration of the salts affected the dry weight gain of some plant parts. Plantlets cultivated in the MS medium obtained better leaf dry weight and total leaf area than plantlets cultivated in half-strength MS. The half-strength MS medium proved to be most effective for root length growth and root dry weight gainin vitro. The growth curve showed that day 30 was the time for subculturing the species. Starting with only one nodal segment, 3125 plantlets were obtained after sixth months of cultivation at a multiplication rate of five. The plantlets of Lippia dulcis were removed from the flasks and acclimatized with success in a greenhouse.<br />Index terms: Growth analysis; micropropagation; shoot proliferation; nodal segment.</p> 2023-03-28T00:00:00-03:00 Copyright (c) 2023 Plant Cell Culture & Micropropagation - ISSN 1808-9909 http://pccm.ufla.br/index.php/plantcellculturemicropropagation/article/view/185 Control of in vitro contamination during the establishment of Pyrus communis explants using Plant Preservative MixtureTM 2022-10-11T19:18:30-03:00 Fernanda Grimaldi fernandagrimaldi@outlook.com Fernanda Espíndola Assumpção Bastos feabastos@hotmail.com <p>The presence of fungal and bacterial contamination in in vitro propagation is a determinant of the culture establishment. The biocide PPM (Plant Preservative Mixture™) has been utilized to control in vitro contamination. According to the manufacture’s label, it is a heat-stable, broad-spectrum product, non-selective, that affects directly microorganisms without causing damage to plant cells. The purpose of this study was to evaluate the influence of PPM asepsis on the control of contamination during the in vitro establishment and survival of Pyrus communis rootstock explants. Six compositions were tested for asepsis and explants from two locations (field and greenhouse). The results showed that asepsis with Alcohol 70% (1 minute) + NaOCl 2.5% + Tween 20 (15 minutes), plus 4.0 ml L-1 PPM added to media performed on explants from greenhouse plants and asepsis, with PPM 5% solution bath and PPM 5% solution bath plus 2.0 ml L-1 PPM added to media performed on explants from field-grown plants presented a good microbial control and good rate of survival.</p> <p>Index terms: Biocide; tissue culture; micropropagation; pear tree; PPM.</p> 2023-03-14T00:00:00-03:00 Copyright (c) 2023 Plant Cell Culture & Micropropagation - ISSN 1808-9909 http://pccm.ufla.br/index.php/plantcellculturemicropropagation/article/view/192 In vitro culture of Stryphnodendron adstringens Mart. Coville 2023-03-30T20:52:30-03:00 Gabriela Ferreira Nogueira gabi_bioufla@hotmail.com Renato Paiva renpaiva@ufla.br Daiane Peixoto Vargas dvbio@hotmail.com Raírys Cravo Herrera rairys@ufpa.br Tainá Teixeira Rocha rochataina@gmail.com Diogo Pedrosa Corrêa da Silva pedrosa_correa@yahoo.com.br <p>Stryphnodendron adstringens (Mart.) Coville is a species native to Cerrado with high medicinal potential. It is an important<br />tannin source, is used mainly due to its healing, anti-inflammatory, and anti-septic activities. Due to the difficulties in<br />sexual propagation, the objective of this work was to study some aspects of its the in vitro culture. The concentration of<br />salts influenced the establishment of the initial explant in vitro, with a higher percentage of germination in the culture<br />medium without salts. The combination of concentrations of 1.0 mg L-1 BAP and 0.1 mg L-1 NAA promoted greater shoot<br />formation, and the concentration of 2.0 mg L -1 IBA promoted greater histogenesis. The composition of the culture medium influenced the establishment and development of S. adstringens.</p> <p><br /><strong>Index terms</strong>: Native Brazilian tree; tissue culture; micropropagation; growth regulator</p> 2023-10-11T00:00:00-03:00 Copyright (c) 2023 Plant Cell Culture & Micropropagation - ISSN 1808-9909 http://pccm.ufla.br/index.php/plantcellculturemicropropagation/article/view/186 Tolerance to desiccation and production of encapsulated units of gabiroba (Campomanesia adamantium) seeds 2022-10-07T15:51:46-03:00 Valéria Prado Braga valeriapb_1@hotmail.com Andréia Vanessa da Silva andreia_v_s_@hotmail.com Lana Laene Lima Dias lanalaene@gmail.com Edésio Fialho dos Reis edesioreis@ufj.edu.br Carla Gomes Machado carlagomesmachado@ufj.edu.br Antônio Paulino da Costa Netto apcnetto@ufj.edu.br Diego Ismael Rocha diego.rocha@ufv.br <p>Campomanesia adamantium is a Brazilian Cerrado fruit crop species that presents a recalcitrant behavior, which compromises the viability of its seeds. Due to this seed feature, the objective of this study was to evaluate the preservation capacity of the species by the use of synthetic seeds. Two seed lots were maintained in a ventilation oven regulated at 30 °C for 30, 60, 120, 240 and 960 min, and then compared with the fresh seeds (control). After drying, the lots were evaluated according to the germination rate, emergence speed index (ESI), initial time, final time and mean time of germination, synchrony, relative frequency, germination speed and seed vigor. For the production of encapsulated units, 3 complexation times (15, 20 and 30 min) and 5 concentrations of sodium alginate (0, 1.5, 2, 2.5 and 3 g) were evaluated, with 3 replicates. For both experiments, Sisvar software was used, and the means were compared by Tukey test at 5%. Seed quality was compromised by desiccation, as the ESI decreases with increasing desiccation time. Regarding synchrony, there was no significant difference among the treatments, whereas for germination time, fresh seeds started and finished the process faster than the others, and the germination time increased as the drying treatments time increases. The emergence rate of fresh seeds was much higher than those exposed to desiccation. For synthetic seeds, the best complexation time was 20 min for 1.5, 2 and 3 g alginate, reaching 100% of the germinated encapsulated units.<br />Index terms: Cerrado fruit crop; recalcitrant seeds; seed germination; synthetic seeds.</p> 2023-03-14T00:00:00-03:00 Copyright (c) 2023 Plant Cell Culture & Micropropagation - ISSN 1808-9909