• Plant Biotechnology Reports
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• v.5 no.1
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• pp.35-43
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• 2011

This communication describes for the first time an efficient and reproducible protocol for large-scale multiplication of Bambusa nutans. Nodal segments collected from field-grown clumps and cultured on Murashige and Skoog (MS) medium supplemented with $4.4{\mu}M$ benzylaminopurine (BA) and $2.32{\mu}M$ kinetin (Kin) gelled with 0.2% gelrite yielded 80% aseptic cultures with 100% bud-break. The in vitro-formed shoots obtained after bud-break were successfully multiplied in MS liquid medium supplemented with $13.2{\mu}M$ BA, $2.32{\mu}M$ Kin, and $0.98{\mu}M$ indole-3-butyric acid (IBA). Sub-culturing of shoots every 3 weeks on fresh multiplication medium yielded a consistent proliferation rate of 3.5-fold. Shoot clusters containing three to five shoots were successfully rooted with 100% success on half-strength MS liquid medium supplemented with $9.8{\mu}M$ IBA, $2.85{\mu}M$ indole-3-acetic acid (IAA), $2.68{\mu}M$ naphthaleneacetic acid (NAA), and 3% sucrose. Plantlets grown in vitro were acclimatized and subsequently transferred to the field. Inter-simple sequence repeat analysis has confirmed the genetic uniformity of the tissue-cultured plants up to 27 passages.

• Journal of Plant Biotechnology
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• v.5 no.4
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• pp.225-231
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• 2003

The hormonal requirement suiting micropropagation of Morus alba during any season throughout the year was studied. Sprouting frequency from axillary buds of M. alba was greatly influenced by the time of explant collection, the highest value was achieved when nodal explants were collected at the end of bud dormancy period (late in March) and cultured on Murashige and Skoog (MS) medium supplemented with low concentration (0.5 mg/L) of BAP, kinetin or IBA (85-68%). In addition, they showed higher axillary bud sprouting on growth-regulators-free medium (49%) than others collected in autumn or winter and cultured on medium supplemented with various growth regulators (47-48%). Regardless of that period, young explants with greenish buds collected in summer exhibiting high sprouting frequency (66%) on MS medium supplemented with 0.5 mg/L kinetin and 0.5 mg/L GA3. Shoot multiplication via adventitious bud formation was achieved when the nodal explants were cultured on MS medium supplemented with 2 mg/L BAP and 0.2 mg/L IBA. Further multiplication via nodal explants of in vitro grown shoots was obtained on MS medium supplemented with 0.5 mglL BAP and 0.5 mg/L GA3. While half strength MS medium supplemented with low concentration (0.5 mg/L) of IBA, IAA or 2,4-D stimulated adventitious root formation, IBA was the best. After transfer the plantlets to the soil, acclimatization for three weeks was essential prerequisite for survival in high frequency (92%). Peroxidase activity is related to break of bud dormancy where maximum enzyme activity was detected when the lateral buds were induced to commence growth under field condition (early in spring) or in vitro.

• Journal of Sericultural and Entomological Science
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• v.30 no.2
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• pp.75-83
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• 1988

These experiments were carried out to define the rest period of mulberry by treating growth regulators in Taegu, Korea. Results obtained were as follows: It was recognized that the depth of rest in Taegu, Korea, was not deeper than that in Tokyo and Kagoshima, Japan. The rest of mulberry was begun at the end of September, subsequently became deeper through the first October into the late October and then turned gradually into quiescence by the beginning of November. Buds sprayed by gibberellic acid ($GA_3$) 10ppm and urea 0.5% were promoted to sprout, while naphthalene acetic acid (NAA) 0.02% inhibited strongly bud sprouting and abscisic acid (ABA) 20ppm had no effect on the rest of mulberry. Gibberellic acid 10ppm enhanced the rate of green color of bud after incubation for 10 days at $30^{\circ}C$. By the portion of mulberry stems, the depth of rest was different that the middle buds were less dormant than those lower. The optimal time required for the mulberry winter bud break is 15 days incubation at $30^{\circ}C$ as treated with $GA_3$.

• Horticultural Science & Technology
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• v.31 no.2
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• pp.141-145
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• 2013

The aim of this study was to investigate the effect of two male cultivars of asparagus with low different chilling periods on bud breaking, relative spear growth rate, shoot number and yield. Four-month-old plants of two male cultivars of asparagus were dried to impose dormancy and placed in a coldroom at $5^{\circ}C$ to satisfy the chilling requirement for 0, 2, 4, and 6 weeks. After the specified chilling time, the pots were placed in greenhouse. The results showed that mean days to bud break of 'Jersey Giant' significantly decreased with an increasing chilling period from 0 to 6 weeks, but 'Jersey Supreme' was not affected. The relative spear growth rate of 'Jersey Supreme' was significantly stimulated by chilling compared to non-chilled plants. Shoot production and total spear weight of 'Jersey Supreme' tended to be greater than 'Jersey Giant' irrespective of chilling treatments. Following low temperature treatment, 'Jersey Supreme' showed shorter dormant period than 'Jersey Giant', faster growth of spear. The present study showed that asparagus male cultivar at duration of chilling treatment had an affirmative effect on bud breaking, spear growth rates, shoot number and yield of asparagus.

• Journal of Plant Biotechnology
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• v.8 no.1
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• pp.51-55
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• 2006

A rapid micropropagation protocol was established for Exacum travancoricum Bedd. The effect of two cytokinins viz. BA and kinetin were studied to evaluate the propagation of plants through nodal explants. MS medium supplemented with 13.32 ${\mu}M$ BA induced early bud break and subsequent production of multiple shoots. Rooting of shoots occurred when cultured on 1/2 strength MS medium supplemented with 14.7 ${\mu}M$ IBA. Rooted plants were acclimatized to greenhouse conditions. The propagated plants were transferred successfully to field with 65% success. As the plant was amenable to propagation in vitro, this can be employed as a tool for conservation of this critically endangered and endemic ornamental herb.

• Korean Journal of Plant Resources
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• v.28 no.3
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• pp.357-362
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• 2015

Carbohydrate sources are one of important factors associated with macro- and micro nutrients and phytohormones in vitro culture medium for shoot growth. The optimal carbohydrates for eight species of the genus Prunus which are economically important fruit crop was evaluated at the initiation and elongation stages. All carbohydrate seemed utilized for the bud break and leaf growth at the early stage of culture. However, shoot elongation and fresh weight of species tested were superior in the medium containing 90 mM of fructose or glucose rather than sucrose. There was no difference between glucose and fructose. Adventitious shoots from the axillary buds were induced in most species but no significant differences were observed except for two species (P. salicina ‘Shiro’ and P. tomentosa). These result demonstrated that glucose and fructose were suitable carbohydrate sources for diverse Prunus species than sucrose, although the response to the carbohydrates in the medium were slightly different in the species.

• Journal of Bio-Environment Control
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• v.23 no.4
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• pp.263-268
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• 2014

This research was performed to investigate the effect of light source and light quality in night break treatment on the growth and flowering of standard chrysanthemum. It was processed 4 hours (22:00-02:00) night break using LED 590, 610, 630, 660, 680nm and fluorescent lamp (mixed light of 480+540+610nm) in standard chrysanthemum 'Baekma' and 'Jinba' for 40 days from transplanting. The days to flower budding from short-day treatment of 'Baekma' were the longgest at fluorescent treatment (21.3 days) and were the shorttest at LED 590nm treatment (15.8 days) among all treatments. The days to flower budding from short-day treatment of 'Jinba' was longger with 18.0 days, 17.8 days, and 17.7 days at the fluorescent, LED 610nm, and 660nm treatments. And it was the shortest with 15.1 days in LED 590nm treatment. Similarly, the days to flowering from short-day treatment of 'Baekma' was the longgest with 56.9 days at fluorescent treatment, and was the shorttest in 51.6 days about LED 590 nm treatment. The days to flowering from short-day treatment of 'Jinba' was longer at fluorescent (56.0 days) and LED 660nm (56.7 days) treatments and was shortest at LED 590nm (52.9 days) among all treatments. Therefore, inhibition of flower bud initiation and flowering were the most effective under fluorescent treatment in case of 'Baekma', and fluorescent and LED 660nm treatments in case of 'Jinba'. The length and weight of cut flower of 'Baekma' and 'Jinba' were most excellent in fluorescent treatment in which the floral differentiation suppression effect was the best. Consequently, as to the growth and flowering of standard chrysanthemum, the treatment which was suitable as the light source and light quality for night break is regarded as the fluorescent lamp, and also under LED 660nm up to a certain level.

• Korean Journal of Medicinal Crop Science
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• v.4 no.3
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• pp.187-192
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• 1996

This study was investigated to know about the stages of flower bud development and the effects of natural and artificial cold treatment on flowering of herbaceous peony. Developing buds of Paeonja lactㅑflora Pall. var. Taebaek were observed since Jun. 17 and peony plants were forced since Nov. 27 in the green house with two weeks interval, and other plants were forced after cold treatment in $5^{\circ}C$ for 1, 2, 4, 6weeks. Differentiation of vegetable part in peony buds was started in early June, and floral part was differentiated in September and their differentiation was continued to shooting in early spring. Buds of peony were sprouted and flowered when it was forced on Dec. 4. Days to shooting were decreased with delay of forcing time from early to late of December, significantly. Two weeks for cold treatment were enough to break dormancy of peony and days to shooting of the cold treated were significantly shorter than the untreated in the same forcing times

• Journal of Bio-Environment Control
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• v.20 no.1
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• pp.45-49
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• 2011

This research was carried out to investigate frost damage of mulberry tree (Morus alba) according to topographic characteristics in Buan province. The first bud-break, leafing, blooming and harvest date of mulberry tree in 2010 were two, four, fourteen and eight days later than those in 2009, respectively. These results were that daily mean temperature during March and April in 2010 were lower than those in 2009 by $2.3^{\circ}C$ and $2.4^{\circ}C$. Frost damage of orchards at flat-bottomed valley, flat near hill and lake, and plain were 50.0%,12.0%, and 4.2%, respectively. Also, frost damage of branch of below 15 mm in diameter was serious than that of branch over 16 mm, but orchard at flat-bottomed valley was high as the range of 46.2~54.0%. These results in 2010 were caused by occurrence of below zero temperatures in leafing stage. Since then, many shoots came out at accessary bud on proximal and the top part of the branches. Therefore, frost damage of mulberry tree in Buan province in 2010 was caused by occurrence of below zero temperatures on April and topographic characteristics of orchard.

• Horticultural Science & Technology
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• v.32 no.3
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• pp.296-302
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• 2014

The foliage of variegated Solomon's seal is excellent in cut flower arrangements. However, it has a restricted marketing period because the harvesting is limited in spring and summer. The increased interest requires the year-round production, thus techniques for dormancy breaking and forcing without low temperature treatment is needed. Therefore, experiments were conducted to d etermine whether gibberellic acid (GA) could break dormancy in variegated Solomon's seal. Thes prouting of dormant bud did not occur throughout the experiment when $GA_3$ $400mg{\cdot}L^{-1}$ was applied to dormant rhizomes as a soil drench. However, when plants were treated with a GA drench after scratch with razor blade or were given direct injection of GA, percent sprouting was increased up to 100 or 83.3%, respectively. However, because treatments with razor or syringe may damage internal organs, we tested another method, scarifying the rhizomes with sodium hypochlorite (NaOCl). Rhizome scarification with 4% NaOCl for 6 or 24 hours followed by drench of $GA_3$ $400mg{\cdot}L^{-1}$ increased the dormancy breaking percentage to 70 or 86.7%, respectively. Moreover, scarified and GA-treated rhizomes produced more leaves than untreated or GA-soil drenched plants in the glasshouse. These results showed the possibility of year-round production of variegated Solomon's seal foliage with rhizome scarification and GA treatments.