2005
DOI: 10.1007/s10535-005-0018-5
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An efficient and rapid in vitro regeneration system for metal resistant cotton

Abstract: In this report we describe the most suitable protocol for callus formation and plant regeneration for cotton. We screened 15 cotton (Gossypium hirsutum L.) genotypes for metal resistance and two of them, Nazilli M-503 (M503) Nazilli 143 (N-143) selected as Cd, Cu and Ni resistant. The cotyledonary nodes from these genotypes were the best explants for regeneration of shoots (more than 90 %) and roots (50 to 70 %). Shoot apex also gave good shoot regeneration (more than 90 %) but their root regeneration efficien… Show more

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Cited by 6 publications
(2 citation statements)
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“…Cotton micropropagation in vitro has been successful in a number of cultivars (Sulekha et al 2000;Jin et al 2006;Sun et al 2006;Tanreer et al 2006). Micropropagation protocols have been developed to use different explant sources, such as shoot apex (Aydin et al 2004;Ozyigit and Gozukirmizi 2009), hypocotyl (Aydin et al 2004;Jin et al 2006;Sun et al 2009), and cotyledonary node (Sulekha et al 2000;Bicakci and Memon 2005); the types of media used can vary in composition, using different concentrations and kinds of plant growth regulators (Zhu and Sun 2000;Mithilesh and Bakesh 2001;Zhang et al 2001;Sakhanokho et al 2005;Sujatha and Sailaja 2005;Zhao et al 2007). …”
Section: Introductionmentioning
confidence: 99%
“…Cotton micropropagation in vitro has been successful in a number of cultivars (Sulekha et al 2000;Jin et al 2006;Sun et al 2006;Tanreer et al 2006). Micropropagation protocols have been developed to use different explant sources, such as shoot apex (Aydin et al 2004;Ozyigit and Gozukirmizi 2009), hypocotyl (Aydin et al 2004;Jin et al 2006;Sun et al 2009), and cotyledonary node (Sulekha et al 2000;Bicakci and Memon 2005); the types of media used can vary in composition, using different concentrations and kinds of plant growth regulators (Zhu and Sun 2000;Mithilesh and Bakesh 2001;Zhang et al 2001;Sakhanokho et al 2005;Sujatha and Sailaja 2005;Zhao et al 2007). …”
Section: Introductionmentioning
confidence: 99%
“…Olgun 'Station' tohumları, Bıçakcı ve Memon (2005) yöntemine göre, %5 sodyum hipoklorit ile 6 dakika sterilize edildikten sonra steril distile su ile 5 dakika boyunca durulanmış ve bu işlem üç kez tekrarlanmıştır (Bicakci ve Memon 2005). Tohumlar steril filtre kağıdı ile kurutulmuş, ardından %3 sakkaroz ve %0,6 agar ile takviye edilmiş bazal Murasige ve Skoog (Murashige ve Skoog 1962) ortamında inkübe edilmiştir.…”
Section: Kültür Ortamlarının Hazırlanması Ve Sterilizasyonuunclassified