2016
DOI: 10.17148/iarjset.2016.3921
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Tissue Culture of Dillenia Philippinensis Rolfe

Abstract: A protocol was established for mass propagation of Dillenia philippinensis Rolfe. by tissue culture using mature seeds as initial explants inoculated in vitro on solid Knudson C with 0.5 mg/L benzyladenine (BA) and naphthalene acetic acid (NAA) (T 1 ). Root calli from the cultured seeds were grown in vitro using solid Murashige and Skoog (MS) culture medium with varying concentrations of BA and NAA. Shoot formation was high in 1.0 mg/L BA and NAA (T 2 ) at 140-175 days of culture. Microcuttings were rooted in … Show more

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Cited by 3 publications
(4 citation statements)
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“…this species has many uses and is rather difficult to find in the wild. According to Lumeran (2016), their seeds do not germinate in its natural habitat due to its hard seed coat. The fruits are utilized as hair cleanser, an excellent source of jam, sauce, and fish flavourings.…”
Section: Conservation Valuementioning
confidence: 99%
“…this species has many uses and is rather difficult to find in the wild. According to Lumeran (2016), their seeds do not germinate in its natural habitat due to its hard seed coat. The fruits are utilized as hair cleanser, an excellent source of jam, sauce, and fish flavourings.…”
Section: Conservation Valuementioning
confidence: 99%
“…Kalus kompak tersebut muncul dari daerah hipokotil kecambah biji yang dibiarkan tumbuh cukup lama pada media WP yang mengandung 1 mg/l BAP. Pada penelitian Lumeran (2016), kalus kompak terbentuk dengan eksplan akar kecambah in vitro pada media MS dengan penambahan berbagai kombinasi konsentrasi BAP dan NAA. Tunas dihasilkan dari regenerasi optimal kalus yang ditanam di media yang mengandung 1 mg/l BAP dan 1 mg/l NAA.…”
Section: B Pembahasanunclassified
“…Kultur jaringan D. phillipinensis juga telah dilakukan oleh Lumeran (2016) melalui perkecambahan in vitro biji pada media Knudson C yang ditambahkan BAP serta NAA, setelah tumbuh kalus, dipindahkan ke media MS yang mengandung BAP serta NAA. Media perbanyakan tunas terbaik adalah MS yang ditambahkan BAP dan NAA pada konsentrasi yang sama yaitu 1 mg/l, namun tunas yang terbentuk masih tidak berbeda nyata dengan 0,5 mg/l dan pengamatan tentang morfologi tunas belum dilakukan.…”
unclassified
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