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  <title>In vitro conservation, regeneration and evaluation of genetic fidelity of threatened Banana cv. Nanjanagud Rasabale (AAB)</title>

      <doi>https://doi.org/10.21276/AATCCReview.2025.13.02.153</doi>
  
  <authors>
      </authors>

      <abstract><![CDATA[<p>Banana cv. Nanjanagud Rasabale (AAB, Silk subgroup) is one of the unique cultivars of Karnataka,<br />
India is now failed to revive its GI (Geographical Indication) tag, the major bane of the cultivar is high<br />
susceptibility to Fusarium wilt caused by Fusarium oxysporum f. sp. cubense (Foc). Hence, there is a need for<br />
the conservation of this elite cultivar from the threat of extinction. Plant germplasm can be conserved by<br />
different approaches one of the valuable biotechnological approaches is in vitro conservation. Laboratory studies<br />
were undertaken to come out with an effective protocol for conserving plantlets through a slow growth process<br />
by media manipulation, viz., by adding different growth retardants. Growth retardants such as ancymidol,<br />
paclobutrazol, abscisic acid, and DMSO at three different concentrations each were supplemented to MS<br />
medium. Among different treatment combinations, MS medium supplemented with DMSO 2.25 ml/l was found<br />
to be most effective by prolonging the period of successive sub-culture (154.53 days) and enabling mid to long-<br />
term conservation of shoot tips. The conserved cultures were regenerated using a standardized medium<br />
comprising MS Basal + 4 mg/l BAP + 0.5 mg/l NAA + 3% sucrose + 0.6% agar-agar. Growth was retrieved<br />
successfully with parameters evaluated. Assessment of genetic stability was performed by using Inter Simple<br />
Sequence Repeat amplification (ISSR) markers. All the 15 ISSR primers amplified unambiguous indicating<br />
monomorphic bands with 100 % monomorphism. Overall, the cultures were conserved by extending the sub-<br />
culture period and prolonged storage life without any genetic variation by using growth retardants.</p>
]]></abstract>
  
  <body><![CDATA[<div class="aatcc-article-container"><div class="aatcc-category-label">Current Issue</div><div class="aatcc-meta-box"><div class="aatcc-doi-wrap">
            <a class="aatcc-doi-btn" href="https://doi.org/10.21276/AATCCReview.2025.13.02.153" target="_blank">https://doi.org/10.21276/AATCCReview.2025.13.02.153</a>
        </div><div class="aatcc-abstract-section">
                <h3>Abstract</h3>
                <div class="aatcc-abstract-text"><p>Banana cv. Nanjanagud Rasabale (AAB, Silk subgroup) is one of the unique cultivars of Karnataka,<br />
India is now failed to revive its GI (Geographical Indication) tag, the major bane of the cultivar is high<br />
susceptibility to Fusarium wilt caused by Fusarium oxysporum f. sp. cubense (Foc). Hence, there is a need for<br />
the conservation of this elite cultivar from the threat of extinction. Plant germplasm can be conserved by<br />
different approaches one of the valuable biotechnological approaches is in vitro conservation. Laboratory studies<br />
were undertaken to come out with an effective protocol for conserving plantlets through a slow growth process<br />
by media manipulation, viz., by adding different growth retardants. Growth retardants such as ancymidol,<br />
paclobutrazol, abscisic acid, and DMSO at three different concentrations each were supplemented to MS<br />
medium. Among different treatment combinations, MS medium supplemented with DMSO 2.25 ml/l was found<br />
to be most effective by prolonging the period of successive sub-culture (154.53 days) and enabling mid to long-<br />
term conservation of shoot tips. The conserved cultures were regenerated using a standardized medium<br />
comprising MS Basal + 4 mg/l BAP + 0.5 mg/l NAA + 3% sucrose + 0.6% agar-agar. Growth was retrieved<br />
successfully with parameters evaluated. Assessment of genetic stability was performed by using Inter Simple<br />
Sequence Repeat amplification (ISSR) markers. All the 15 ISSR primers amplified unambiguous indicating<br />
monomorphic bands with 100 % monomorphism. Overall, the cultures were conserved by extending the sub-<br />
culture period and prolonged storage life without any genetic variation by using growth retardants.</p>
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