2015
DOI: 10.21273/hortsci.50.6.888
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Propagation Methods Affect Fruit Morphology and Antioxidant Properties but Maintain Clonal Fidelity in Lowbush Blueberry

Abstract: Means within columns and parameters followed by different letters indicate significant differences at P # 0.05. DPPH = 2,2-diphenyl-1-picrylhydrazyl; GAE = gallic acid equivalents; CE = catechin equivalents; C3GE = cyanidine-3-glucoside equivalents; F.F. = fresh fruit; PM = propagation methods; TC = tissue culture; GS = growing seasons.

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Cited by 26 publications
(67 citation statements)
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“…At least three plants were selected randomly for each cultivar, and the leaves from each cultivar were collected in a replication of three from each plant. Five hundred milligrams of pre-frozen leaves from each plant were homogenized in a FastPrep-24 Tissue and Cell Homogenizer (MP Biomedicals, Irvine, CA, USA) in 80% aqueous acetone solution with 0.2% formic acid (1: 4 g/mL) 26 . The homogenate was kept for slow agitation at 4 °C for 30 min and then centrifuged at 13,000 rpm for 15 min at 4 °C using Allegra 64R (Beckman Coulter Inc., Palo Alto, CA, USA) before collecting the supernatant.…”
Section: Methodsmentioning
confidence: 99%
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“…At least three plants were selected randomly for each cultivar, and the leaves from each cultivar were collected in a replication of three from each plant. Five hundred milligrams of pre-frozen leaves from each plant were homogenized in a FastPrep-24 Tissue and Cell Homogenizer (MP Biomedicals, Irvine, CA, USA) in 80% aqueous acetone solution with 0.2% formic acid (1: 4 g/mL) 26 . The homogenate was kept for slow agitation at 4 °C for 30 min and then centrifuged at 13,000 rpm for 15 min at 4 °C using Allegra 64R (Beckman Coulter Inc., Palo Alto, CA, USA) before collecting the supernatant.…”
Section: Methodsmentioning
confidence: 99%
“…Total phenolic content was determined following photometric technique using the Folin-Ciocalteu method 27 , following Goyali et al . 26 . To obtain the final concentration 200 µg/mL, the crude extracts of polyphenolics were dissolved in methanol.…”
Section: Methodsmentioning
confidence: 99%
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“…Some challenges in this production are a very low rooting percentage in many genotypes, the amount of time required to propagate and commercialize newly-released cultivars for mass propagation [8,9], and phytosanitary problems. In vitro culture (micropropagation) can overcome the limitations of traditional cuttings, presenting an alternative for faster growth [10] Horticulturae 2019, 5, 24 2 of 14 throughout the year (with no seasonal effects) without pathogens [11]. There are some studies on the in vitro propagation of Vaccinium species, but only some of these have been done with rabbiteye (V. virgatum Ait.…”
Section: Introductionmentioning
confidence: 99%
“…For example, tissue culture propagation had a significant effect on morphology and antioxidant metabolites in lowbush blueberry (Vaccinium angustifolium Ait.) compared with the use of cuttings, although the researchers did not identify any genetic changes in the 20 SSRs assessed (Goyali et al, 2015). Although not a replacement, in vitro tissue culture is one tool that may be used to supplement living collections by providing backups of plants in the ground.…”
Section: Complementary Conservation Measuresmentioning
confidence: 99%