The importance of explant source on regeneration and micropropagation of Gladiolus by liquid shake culture

2004 ◽  
Vol 102 (4) ◽  
pp. 407-414 ◽  
Author(s):  
Duong Tan Nhut ◽  
Jaime A. Teixeira da Silva ◽  
Phan Xuan Huyen ◽  
K.Y. Paek
Keyword(s):  
Shake Culture ◽  
Explant Source

Effect of Medium Composition and Explant Source on the Distribution Profiles Selected Micronutrients in Mistletoe Tissue Cultures

2003 ◽  
Vol 26 (2) ◽  
pp. 369-397 ◽  
Author(s):  
S. Kintzios ◽  
M. Barberaki ◽  
J. Drossopoulos ◽  
P. Turgelis ◽  
J. Konstas
Keyword(s):  
Medium Composition ◽  
Tissue Cultures ◽  
Explant Source

scholarly journals Ultrastructural calli analysis of Inga vera Willd. subsp. Affinis (DC.) T.D. Penn

2010 ◽  
Vol 34 (5) ◽  
pp. 789-796 ◽  
Author(s):  
Vanessa Cristina Stein ◽  
Renato Paiva ◽  
Daiane Peixoto Vargas ◽  
Fernanda Pereira Soares ◽  
Eduardo Alves ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Culture Medium ◽  
Cell Development ◽  
Nodal Segments ◽  
Nodal Segment ◽  
Ms Medium ◽  
Flower Buds ◽  
Embryo Formation ◽  
Transmission Electron ◽  
Explant Source

Subcellular changes are relevant to understand plant organogenesis and embryogenesis in the early stages of cell development. The cytology during cell development in tissue culture is however still poorly characterized. This study aimed to characterize the ultrastructural differences related to callogenesis of anthers, ovaries, leaf and nodal segments of Inga vera Willd. subsp. Affinis (DC.) T.D. Penn. Flower buds, nodal segments and leaves were disinfected and inoculated in test tubes containing MS medium with 3% sucrose and 4.5µM 2.4-D, except for leaf callogenesis, where 9µM of this auxin was used, and for the callogenesis of anthers and ovaries, where the culture medium was enriched with 0.25% activated charcoal and 90µM PVP. After 45 days in culture medium, the anther, ovary, leaf and nodal segment calli were fixed in Karnovisky and prepared for visualization by scanning and transmission electron microscopy. Ultrastructural differences were observed among the callus cells of anthers, ovaries, segments and leaves. There was no evidence of somatic embryo formation in the anther, leaf and nodal segment calli, in spite of some embryogenic characteristics in the cells. The ovary calli, with indications of embryo formation, seem to be the most responsive explant source for embryogenesis.

scholarly journals Genetic Variation Analysis of Hevea brasiliensis Genotype Population of In Vitro Micro-Cutting Culture by RAPD Marker

2020 ◽  
Vol 4 (2) ◽  
pp. 57-62
Author(s):  
IRFAN MARTIANSYAH ◽  
NURHAIMI HARIS ◽  
TATI HUSNIYATI ◽  
EDI DJAUHARI PURWAKUSUMAH
Keyword(s):  
Genetic Similarity ◽  
Growth Response ◽  
Random Amplified Polymorphic Dna ◽  
Rapd Marker ◽  
Culture Technique ◽  
Similarity Coefficients ◽  
Micro Cutting ◽  
Explant Source ◽  
Dna Fragment

The rubber seeds are insufficient for producing rootstocks to rubber grafting. It can be overcome by an in vitro micro-cutting culture technique developed in the Indonesian Research Institute for Biotechnology and Bioindustry (IRIBB). However, the origin clone of 57 rubber genotypes used as an explant source in vitro micro-cutting culture is not recognized. The study was to investigate the 57 genotypes that came from mixed GT 1, PB 260, and RRIM 600 as parent clones. We investigated using seven primers of Random Amplified Polymorphic DNA (RAPD), i.e., OPA 02, OPA 07, OPA 15, OPB 04, OPC 05, OPC 11, and OPC 20. The qualitative analyzed by electrophoresis 1% gel agarose. A total of 47 DNA fragments produced with an average of 7 fragments per primer. OPA 02 generated of 13 fragments, whereas OPB 04 only one fragment. The DNA fragment pattern shows the presence of polymorphism. The genetic similarity coefficients obtained in the range of 62-96%. The highest genetic similarity (96%) is genotype 70 and 78. It recognized that 42 genotypes from 57 rubber genotypes had the closest relationship with PB 260 clones. Furthermore, six genotypes had a significant growth response as an explant in vitro micro-cutting culture.

scholarly journals Effect of explant source, perlite nanoparticles and TiO2/perlite nanocomposites on phytochemical composition of metabolites in callus cultures of Hypericum perforatum

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
R. Ebadollahi ◽  
S. Jafarirad ◽  
M. Kosari-Nasab ◽  
S. Mahjouri
Keyword(s):  
Volatile Compounds ◽  
Culture Medium ◽  
Hypericum Perforatum ◽  
Callus Cultures ◽  
Growth Characteristics ◽  
Phytochemical Composition ◽  
Adverse Impacts ◽  
Explant Source ◽  
Metabolite Profiles

Abstract It appears that the biologically-synthesized nanoparticles (NPs) have potential to perform as effective elicitors for the production of valuable secondary metabolites in plants. Besides, it has been reported that the toxicity of the biologically-synthesized NP is not as much as that of the chemically-synthesized NPs. Therefore, it is necessary to test their advantages aspects. In this study, the physical synthesis of perlite NPs and biologically-synthesis of TiO2/perlite nanocomposites (NCs) were conducted. Subsequently, their effects and explant source influence on the growth characteristics and secondary metabolite profiles of Hypericum perforatum callus cultures were evaluated. According to the obtained results, morphology of the synthesized perlite NPs and TiO2/perlite NCs were mesoporous and spherical with sizes ranging about 14.51–23.34 and 15.50–24.61 nm, respectively. Addition of perlite NPs and TiO2/perlite NCs to the culture medium at the concentration range of 25–200 mg/L showed no adverse impacts on the growth characteristics of H. perforatum calli. According to the GC-MS analysis, the stress caused by perlite NPs and TiO2/perlite NCs led to an increase in the variety, amount and number of volatile compounds. The calli obtained from in vitro grown plants produced more volatile compounds relative to the calli obtained from field grown plants under the nanomaterial stress conditions. The production of hypericin and pseudohypericin were also determined in the callus cultures under desired nanomaterials elicitation. Accordingly, our results suggest that perlite NPs and TiO2/perlite NCs can possibly be considered as effective elicitors for the production of volatile compounds, hypericin, and pseudohypericin in callus cultures of H. perforatum.

Effect of Other Toxigenic Mold Species on Aflatoxin Production by Aspergillus flavus in Sterile Broth Shake Culture

1988 ◽  
Vol 51 (6) ◽  
pp. 449-451 ◽  
Author(s):  
PHILIP B. MISLIVEC ◽  
MARY W. TRUCKSESS ◽  
LEONARD STOLOFF
Keyword(s):  
Aspergillus Flavus ◽  
Pure Culture ◽  
Aflatoxin Production ◽  
Penicillium Citrinum ◽  
Aspergillus Ochraceus ◽  
Growth Media ◽  
Shake Culture ◽  
Apparent Effect ◽  
Penicillium Species ◽  
Heat Stable

The effect of Aspergillus ochraceus, A. versicolor, Penicillium citrinum, P. cyclopium and P. urticae on production of aflatoxin by A. flavus when grown together with A. flavus in rotary shake culture was investigated. The two aspergilli had no apparent effect on aflatoxin production, whereas all three Penicillium species substantially lowered aflatoxin production. The toxins that these penicillia produced when growing in pure culture were not found when the penicillia were grown with A. flavus. However, these toxins had no effect on aflatoxin production added to the growth media, nor did the three molds metabolize aflatoxin. When A. flavus was grown in both filter- and autoclave-sterilized filtrates of these three species, no aflatoxins were produced, although A. flavus grew well. These results suggest that although A. ochraceus and A. versicolor have no apparent effect on aflatoxin production, P. citrinum, P. cyclopium and P. urticae produce heat-stable, nonfilterable metabolite(s) which inhibit(s) aflatoxin production by actively growing A. flavus.

scholarly journals Optimization of a protocol for the micropropagation of pineapple

2002 ◽  
Vol 24 (2) ◽  
pp. 296-300 ◽  
Author(s):  
WELITON ANTONIO BASTOS DE ALMEIDA ◽  
GESSIONEI SILVA SANTANA ◽  
ADRIANA PINHEIRO MARTINELI RODRIGUEZ ◽  
MARIA ANGÉLICA PEREIRA DE CARVALHO COSTA
Keyword(s):  
Liquid Medium ◽  
Shoot Proliferation ◽  
Axillary Buds ◽  
Ananas Comosus ◽  
Ms Medium ◽  
Sterile Water ◽  
Calcium Hypochlorite ◽  
Shoot Bud ◽  
Explant Source ◽  
Growth Room

The present work aimed at maximizing the number of plantlets obtained by the micropropagation of pineapple (Ananas comosus (L.) Merrill) cv. Pérola. Changes in benzylaminopurine (BAP) concentration, type of medium (liquid or solidified) and the type of explant in the proliferation phase were evaluated. Slips were used as the explant source, which consisted of axillary buds obtained after careful excision of the leaves. A Sterilization was done in the hood with ethanol (70%), for three minutes, followed by calcium hypochlorite (2%), for fifteen minutes, and three washes in sterile water. The explants were introduced in MS medium supplemented with 2mg L-1 BAP and maintained in a growth room at a 16h photoperiod (40 mmol.m-2.s-1), 27 ± 2ºC. After eight weeks, cultures were subcultured for multiplication in MS medium. The following treatments were tested: liquid x solidified medium with different BAP concentrations (0.0, 1.5 or 3.0 mg L-1), and the longitudinal cut, or not, of the shoot bud used as explant. The results showed that liquid medium supplemented with BAP at 1.5 mg L-1, associated with the longitudinal sectioning of the shoot bud used as explant presented the best results, maximizing shoot proliferation. On average, the best treatment would allow for an estimated production of 161,080 plantlets by the micropropagation of the axillary buds of one plant with eight slips and ten buds/slips, within a period of eight months.

scholarly journals A tryptophan C-methyltransferase involved in streptonigrin biosynthesis in Streptomyces flocculus

1984 ◽  
Vol 220 (1) ◽  
pp. 309-313 ◽  
Author(s):  
D L Hartley ◽  
M K Speedie
Keyword(s):  
High Pressure ◽  
Liquid Chromatography ◽  
Amino Acid ◽  
Stationary Phase ◽  
High Pressure Liquid Chromatography ◽  
Absolute Configuration ◽  
Specific Activity ◽  
Shake Culture ◽  
Methyl Group ◽  
The Absolute

A C-methyltransferase that catalyses the transfer of a methyl group from S-adenosylmethionine to C-3 of tryptophan, resulting in beta-methyltryptophan, has been identified in cell-free extracts of streptonigrin-producing Streptomyces flocculus. The absolute configuration of the product was shown to be (2S,3R)-beta-methyltryptophan by high-pressure liquid chromatography and reactivity with D- and L-amino acid oxidases. In shake culture, maximum specific activity occurs after S. flocculus enters stationary phase, but before significant streptonigrin accumulates.

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