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"Penelitian mengenai eksplorasi senyawa aktif kapang endofit dari tumbuhan mangrove dan aplikasinya sebagai bioinsektisida telah dilakukan. Sebanyak 110 kapang endofit telah diperoleh dari akar, ranting, daun, dan serasah Rhizophora mucronata, Avicennia marina, dan Soneratia alba menggunakan enam jenis media dan lima jenis metode isolasi. Lima dari 110 isolat kapang endofit menunjukkan toksisitas tertinggi (menyebabkan mortalitas lebih dari 90% pada konsentrasi 80 ppm) terhadap larva Artemia salina. Kelima isolat kapang tersebut diidentifikasi berdasarkan data sequence daerah ITS rDNA dan pengamatan morfologi sebagai Emericella nidulans (BPPTCC 6035 dan BPPTCC 6038), Aspergillus flavus (BPPTCC 6036), A. tamarii (BPPTCC 6037), dan A.versicolor (BPPTCC 6039). Hasil pengujian aktivitas insektisida ekstrak etil asetat dari kultur filtrat biakan kelima strain kapang tersebut pada medium cair malt extract terhadap larva neonate dan instar III Spodoptera litura menunjukkan aktivitas sebagai racun lambung, racun kontak, attractant, racun saraf, dan menghambat perkembangan larva. Karakterisasi senyawa aktif dengan metode thin layer chromatography (TLC) yang dikombinasikan dengan beberapa reagen menunjukkan bahwa kelima ekstrak mengandung senyawa triterpenoid yang mengandung saponin; ekstrak yang dihasilkan oleh E. nidulans BPPTCC 6038 mengandung senyawa fenol; dan keempat ekstrak lain mengandung senyawa alkaloid. Formulasi dilakukan dengan menambahkan senyawa adjuvant berupa aseton sebagai pelarut, Tween 80 sebagai surfaktan, dan PEG 6000 sebagai sticker agent. Hasil pengujian aktivitas kelima formulasi terhadap larva neonate dan instar III S. litura menunjukkan bahwa seluruh formulasi memiliki aktivitas insektisida terhadap larva instar III S. litura lebih baik dibandingkan dengan kontrol positif, DeltametrinR (25 g/L).

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A study on the exploration of active compounds from mangrove endophytic fungi and their application as bioinsecticides was conducted. The isolation of mangrove endophytic fungi from roots, twigs, leaves, and leaf litter from Rhizophora mucronata, Avicennia marina, and Soneratia alba was conducted using a combination of six media with five isolation methods. Five of the 110 mangrove endophytic fungal isolates showed the highest toxicity (causing more than 90% larval mortality at 80 ppm) on Artemia salina larvae. Based on the DNA sequence data of the internal transcribed spacers (ITS) region of ribosomal DNA and morphological characteristics, these isolates were identified as Emericella nidulans (BPPTCC 6035 and BPPTCC 6038), Aspergillus flavus (BPPTCC 6036), A. tamarii (BPPTCC 6037), and A. versicolor (BPPTCC 6039). A bioassay on Spodoptera litura neonate and third instars larvae showed that five ethyl acetate of the five fungal filtrate extracts from malt extract broth medium exhibited attractant and insecticidal activities through stomach poisons, contact poisons, neurotoxins, and the inhibition of larval and pupal development. The chemical characterization of the five extracts using thin layer chromatography (TLC) combined with several reagents showed that the five extracts contained triterpenoid with saponin compounds, the extract from E. nidulans (BPPTCC 6038) contained phenolic compounds, and the four other extracts contained alkaloid compounds. Formulations were conducted by the addition of adjuvant: acetone as the solvent, Tween 80 as the surfactant, and PEG 6000 as the sticker agent. The insecticidal activity from five formulations on S. litura third instars larvae showed that the five formulations exhibited better insecticidal activity than DeltamethrinR (25 g/L) as the positive control."

"Penelitian bertujuan untuk memperoleh isolat-isolat khamir, memperoleh informasi spesies-spesies khamir yang berasal dari lebah madu Apis cerana dan substrat terkait, dan mengetahui pengaruh pemberian pollen substitute (PS) terhadap produktivitas koloni A. cerana. Khamir diisolasi dari telur, larva, pupa, lebah pekerja, lebah ratu, lebah jantan serta bee pollen, bee bread dan madu A. cerana, serta nektar dan serbuk sari dari bunga-bunga yang dikunjungi A. cerana. Khamir diisolasi menggunakan medium YMA dan YMA+sukrosa 50%. Identifikasi khamir dilakukan berdasarkan data sequence daerah internal trancribed spacer ribosomal DNA (ITS rDNA), analisis filogenetik dilakukan dengan metode Neighbor Joining, serta karakter morfologi dan fisiologi-biokimia. Sebanyak enam variasi PS dibuat untuk menguji preferensi A. cerana terhadap jenis PS. PS dalam bentuk pasta diberikan setiap hari selama 20 hari. Pengujian pengaruh pemberian variasi PS lokal dan PS impor terhadap produktivitas koloni A. cerana dilakukan selama 13 minggu. Sebanyak 1.409 isolat khamir diperoleh dari A. cerana dan substrat terkait. Lima puluh isolat representatif diseleksi untuk diidentifikasi. Hasil identifikasi menunjukkan bahwa 50 isolat khamir tersebut terdiri dari 12 genera dan 21 spesies. Sebanyak enam genera termasuk ke dalam phylum Ascomycota (class Hemiascomycetes, order Saccharomycetales),dan enam genera lainnya termasuk ke dalam phylum Basidiomycota (classes: Hymenomycetes, Urediniomycetes, dan Ustilaginomycetes). Hasil penelitian mengindikasikan adanya asosiasi dan interaksi antara spesies khamir dengan lebah madu. Hasil uji preferensi terhadap enam variasi PS lokal menunjukkan PS yang mengandung Candida hawaiiana CR015 asal bunga Brugmansia suaveolens (PS1) dan PS yang mengandung baker?s yeast (PS4) lebih disukai oleh A. cerana dibandingkan PS lain. Hasil uji produktivitas menunjukkan pollen substitute yang mengandung Candida hawaiiana CR015 asal bunga Brugmansia suaveolens (PS1) terbukti potensial dalam meningkatkan produktivitas koloni A. cerana setara dengan pollen substitute impor.

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The aims of this study were to obtain yeast isolates, to get species information from honeybee Apis cerana and related substrates, and to determine the effects of a pollen substitute (PS) on the productivity of A. cerana colonies.Yeasts were isolated from A. cerana eggs, larvae, pupae, workers, queens, drones, bee pollen, bee bread, honey, and nectars and pollens from flowers visited by A. cerana. The media used to isolate the yeasts were Yeast-Extract Malt-Extract Agar (YMA) and YMA+50% sucrose.

The yeasts were identified based on sequence data of internal transcribed spacer regions of ribosomal DNA (ITS rDNA). Phylogenetic analysis of yeasts based on ITS rDNA sequence data was performed by the neighbor-joining method. Morphological, physiological and biochemical characteristics of yeasts were observed. To determine the preference of A. cerana for pollen substitutes, honeybee colonies were fed daily with six varieties of pollen substitutes in patty form for 20 days. To examine the effects of pollen substitutes on the productivity of A. cerana, honeybee colonies were fed on local pollen substitutes (PSs) and imported PS for 13 weeks. A total of 1,409 yeast isolates were obtained from various substrates. Fifty representative isolates were selected for identification. The identification results showed that those 50 yeast isolates consisted of 12 genera and 21 species. Six of these genera belong to phylum Ascomycota, and class Hemiascomycetes, while the other six genera belong to phylum Basidiomycota and classes Hymenomycetes, Urediniomycetes and Ustilaginomycetes.

This study indicated that there is an association and an interaction between yeast species and honeybee. The preference test result showed that a PS containing Candida hawaiiana CR015 isolated from the flower of Brugmansia suaveolens (PS1) and a PS containing baker?s yeast (PS4) were favoured by A. cerana colonies.

The productivity test result showed that a PS containing Candida hawaiiana CR015. The preference test result showed that a PS containing Candida hawaiiana CR015 isolated from the flower of Brugmansia suaveolens (PS1) and a PS containing baker?s yeast (PS4) were favoured by A. cerana colonies. The productivity test result showed that a PS containing Candida hawaiiana CR015 isolated from the flower of Brugmansia suaveolens (PS1) was proved to potentially increase the productivity of A. cerana colonies and could be considered as good as imported pollen substitute."