Abstract:The present study was conducted at the Biotechnology Laboratory, Biotechnology Division, Bangladesh Agricultural Research Institute (BARI), Gazipur during the period from September 2004 to June 2005 to investigate the effect of different concentrations of BAP and NAA on virus free plant regeneration, shoot multiplication and different concentrations of IBA and IAA on in vitro root formation of banana cv. BARI Banana-I. The culture meristem first turned brown in colour in 4-5 days which grew into a green globul… Show more
“…These findings did not agree with the results of Al-Amin et al [25], where the MS media supplemented with BAP and NAA in their study showed different results for increasing shoot length Interactive effect of BAP and IAA was also observed in fresh weight (Figure 2). The media with 6 mg/l of BAP in combination with 0.35 mg/l IAA, significantly (p ≤ 0.01) resulted in high fresh weight as compared with other treatments ( Table 3).…”
The aim of this study was to investigate the effects of concentration of different growth regulators (auxins and cytokinins) on growth and development of banana shoot tips cultured in vitro. Explants were taken from young suckers of field grown plants of var. "Yangambi". The shoot tips were cultured on MS media supplemented with different concentrations of BAP (0, 2, 4, 6 and 8 mg/l) with or without IAA at concentration of 0.34 mg/l. At the rooting phase, the media was supplemented with different concentrations of IBA (0.1, 0.5, 1.0, 1.5 and 2.0 mg/l) with or without BAP at concentration of 0.2 mg/l. The results indicated that 6.0 mg/l BAP significantly increased the number of shoots formed and the interaction of 6 mg/l BAP with 0.35 mg/l IAA significantly increased the fresh weight. For rooting, 2.0 mg/l IBA was more efficient in number and length of roots produced than all other treatments.
“…These findings did not agree with the results of Al-Amin et al [25], where the MS media supplemented with BAP and NAA in their study showed different results for increasing shoot length Interactive effect of BAP and IAA was also observed in fresh weight (Figure 2). The media with 6 mg/l of BAP in combination with 0.35 mg/l IAA, significantly (p ≤ 0.01) resulted in high fresh weight as compared with other treatments ( Table 3).…”
The aim of this study was to investigate the effects of concentration of different growth regulators (auxins and cytokinins) on growth and development of banana shoot tips cultured in vitro. Explants were taken from young suckers of field grown plants of var. "Yangambi". The shoot tips were cultured on MS media supplemented with different concentrations of BAP (0, 2, 4, 6 and 8 mg/l) with or without IAA at concentration of 0.34 mg/l. At the rooting phase, the media was supplemented with different concentrations of IBA (0.1, 0.5, 1.0, 1.5 and 2.0 mg/l) with or without BAP at concentration of 0.2 mg/l. The results indicated that 6.0 mg/l BAP significantly increased the number of shoots formed and the interaction of 6 mg/l BAP with 0.35 mg/l IAA significantly increased the fresh weight. For rooting, 2.0 mg/l IBA was more efficient in number and length of roots produced than all other treatments.
“…The above mentioned results are in agreement with those of Gübbük and Pekmezci (2004), Gubbuk and Pekmezci (2006), Kalimuthu et al (2007), Shiragi et al (2008), Al-Amin et al (2009), Bhosale et al (2011), Mahadev et al (2011, Jafari et al (2013), Rahman et al (2013), Anbazhagan et al (2014), Mahdi et al (2014), Ngomuo and Ndakidemi (2014) and Shankar et al (2014). All of them found that BAP and kinetin increased the shoot number initiated from shoot tips of banana during micropropagation through tissue culture.…”
Banana (Musa spp. family Musaceae) is a fourth most important fruit crop in the world. This investigation was carried out in tissue culture laboratory in Horticulture Department, Agriculture Faculty, Suez Canal University, Ismailia during the period 2013 -2015, to study the effect of medium type (solid or liquid) and cytokinin types (BAP or Kin at 0, 1, 3, 5, 7 mg/l) during multiplication stage, in a complete randomized design with two factors. The explants were collected from suckers grown around banana fruiting mother plants, cultivar Grande Naine. In liquid medium supplemented with 3.0 mg/l Benzyl amino purine (BAP) increased number of shoots (7.20). While 5 mg/l Kinetin (Kin) improved shoot length (7.40 cm) in solid medium compared with other treatments. The liquid media is preferable within mass production and commercial advantages. The BAP promotes shoot initiation and development either with solid or liquid media more than Kin.
“…Long generation time, various levels of ploidy, lack of genetic variability, and sterility of most edible cultivars have hampered the development of disease-resistant Musa by conventional breeding (Stover and Buddenhagen 1986;Stover and Simmonds 1987;Swennen and Vuylsteke 1993;Musoke et al 1999;Pillay et al 2004;Tripathi et al 2004). In vitro micropropagation has played a key role in clonal propagation of banana for obtaining large numbers of homogenous plants and breeding of plantains and bananas (Pierik 1987;Rowe and Rosales 1996;Vuylsteke et al 1997;Kalimuthu et al 2007;Al-Amin et al 2009). …”
In vitro propagation has played a key role for obtaining large numbers of virus free, homogenous plants, and for breeding of plantains and bananas (Musa spp.). Explant sources utilized for banana micropropagation include suckers, shoot tips, and floral buds. The present study employed male floral meristems as explant material for micropropagation of hill banana ecotypes (AAB) 'Virupakshi' and 'Sirumalai.' Immature male floral buds were collected from healthy plants from hill banana growing areas. Exposure of explants to ethyl alcohol (70%, v/v) for 30 s, then mercuric chloride (0.1%, w/v) for 30 s, followed by three independent rinses of 5 min each in autoclaved, double-distilled water satisfactorily reduced the contamination. Male floral bud explants were cultured on Murashige and Skoog (MS) basal medium supplemented with different combinations of 6-benzylaminopurine (BAP), coconut water, naphthaleneacetic acid, gibberellic acid, and additional supplements. MS medium supplemented with 5 mg l −1 BAP and coconut water (15%) was the most efficient media for shoot initiation and multiple shoot formation (15 shoots from a single part of a floral bud). The best response for shoot elongation was obtained using the combination of basal MS, 5 mg l −1 BAP, 1 mg l −1 naphthaleneacetic acid and 1.5 mg l −1 gibberellic acid. Regenerated shoots were rooted in basal MS medium within 15-20 d. The rooted plantlets were transferred to a soil mixture and maintained at a temperature of 25±2°C for 10 d and then at room temperature (30-32°C) for 2 wk, before transferring to a greenhouse. The regenerated plantlets showed 100% survival.
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