Abstract

Eucalyptus pellita is fast growing species and have many advantages such as: pulp and paper industry raw material, building construction, charcoal, and medicine. The research was carried out to study plant morphogenesis from shoot explant of E. pellita F. Muell by in vitro technique. The experiment was conducted at Tissue Culture Laboratory, Agriculture Faculty of Mulawarman University from March until June, 2016.Single factor experiment was arranged in Completely Randomized Design with 10 replications. The factor was BAP concentrations (B) consisted of 1.00 mg BAP L-1 (b1); 2.00 mg BAP L-1 (b2); 3.00 mg BAP L-1 (b3); and 4,00 mg BAP L-1 (b4). The explants was innoculated on MS medium supplemented with BAP according to the treatments. Data analyzed by analysis of variance (anova) and continued by Least Significant Difference (LSD) test with level 5%. Results of the experiment showed that the BAP concentrations can promote shoot formation of E. pellita. Statistical analysis indicated that the effect of BAP concentrations significantly difference on number of shoots at 8 weeks after innoculation (WAI), shoot length, and number of leaves at 4; 6; and 8 WAI, however it’s no significantly difference on shoot formation time and number of shoots at 4 and 6 WAI. The highest number of shoots, shoot length, and number of leaves achieved by 4,00 mg BAP L-1.

Highlights

  • Eucalyptus pellita is a fast growing species and has many advantages such as pulp and paper industry raw material, building construction, charcoal, and medicine

  • The experiment was conducted at Tissue Culture Laboratory

  • The explants were inoculated on Murashige dan Skoog (MS) medium supplemented with

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Summary

METODE PENELITIAN

Penelitian dilaksanakan di Laboratorium Kultur Jaringan Fakultas Pertanian Universitas Mulawarman Samarinda. Bahan yang digunakan terdiri atas eksplan tunas E. pellita, ZPT Benzil Amino Purin (BAP), media Murashige dan Skoog (MS), bahan-bahan sterilisasi (Dithane M45, Bayclin, Sunlight cair, Betadin, Tween, alkohol 90%, alkohol 70% dan spiritus), tissue, kapas, plastic wrap, plastik gulung dan karet gelang. Alat yang dipakai terdiri atas autoclave, laminar air flow cabinet, botol kultur, timbangan analitik, pH meter/pH indicator, alat-alat bedah, hot plate, kompor gas, gelas ukur, botol erlenmeyer dan petridish. Eksplan tunas disterilisasi menggunakan fungisida dan Bayclin, selanjutnya dibilas dengan air steril. Eksplan steril dipotong-potong di dalam laminar air flow dan ditanam pada media dasar MS yang ditambah ZPT BAP sesuai perlakuan. Kultur diinkubasi pada kondisi terang selama 24 jam, sedangkan subkultur dilakukan setiap empat minggu. Sidik ragam dilakukan untuk mengetahui pengaruh konsentrasi BAP, apabila hasil sidik ragam menunjukkan pengaruh yang berbeda nyata, untuk membandingkan antara dua rata-rata perlakuan dilakukan uji Beda Nyata Terkecil (BNT) pada taraf 5%

HASIL DAN PEMBAHASAN
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KESIMPULAN DAN SARAN
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Fakultas Pertanian
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