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Menara Perkebunan
ISSN : 01259318     EISSN : 18583768     DOI : -
Core Subject : Agriculture,
Menara Perkebunan as a communication medium for research in estate crops published articles covering original research result on the pre- and post-harvest biotechnology of estate crops. The contents of the articles should be directed for solving the problems of production and/or processing of estate crops of smallholder, private plantations and state-owned estates, based on the three dedications of plantation. Analyses of innovative research methods and techniques in biotechnology, which are important for advancing agricultural research. Critical scientific reviews of research result in agricultural and estate biotechnology.
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Articles 5 Documents
Search results for , issue "Vol 80, No 1: Juni 2012" : 5 Documents clear
Dinamika populasi Trichoderma harzianum DT38 pada campuran arang hayati tandan kosong kelapa sawit (TKKS) dan gambut Population dinamic of Trichoderma harzianum DT38 on mixture of empty fruit bunches of oil palm (EFBOP) biochar and peat Irma KRESNAWATY; Sayhas SUHADA; Asmini BUDIANI; T W DARMONO
E-Journal Menara Perkebunan Vol 80, No 1: Juni 2012
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (281.329 KB) | DOI: 10.22302/iribb.jur.mp.v80i1.45

Abstract

Abstract Biochar offers option for managing land as a source  of carbon and soil conditioner. The ability of biochar in  increasing soil  fertility associates with its ability to retain water, reduce soil acidity, and keep the availability of essential nutrients for plant thus increasing crop produc-tivity, and reducing the risk of soil erosion. Biochar is also substance to provide a  suitable environment for the growth of beneficial microbes, including an isolate of  Trichoderma harzianum used in this study, that has been proven capable in stimulating plant growth and suppressing soil borne diseases. The purpose of this research was to determine the in vitro compatibility of T. harzianum DT38, Indonesia Biotech-nology Research Institute for Estate Crop (IBRIEC) collection, in mixtures of  EFBPO biochar and peat during 28 days. This research was performed in completely randomized design with single factor, comprising of five formulas: 1) 100% EFBOP biochar (K1), 2) 100% peat (K2), 3) Mixture of EFBOP biochar and peat = 1 : 4 (F1), 4) Mixture of EFBOP biochar and peat=  1 : 8 (F2), dan 5) Mixture of EFBOP biochar and peat=  1 : 12 (F3). The colony forming units were determined after storage to express the amount of fungal propaguls in each mixture. The results was analized using one-way ANOVA test and Duncan Test. Result showed that the total of  T. harzianum DT38 propaguls was not significantly difference among five mixture preparations tested during 0 and 7 days storage. The total propaguls were insignificantly difference between F1 and K2, and also between  F2 and F3in 14, 21 and 28 days incubation. Peat addition on biochar increased the total of  T. harzianum DT38 propaguls during 28 days incubation. The total propaguls which are remain high in F1, F2 and F3 formula up to 28 days storage indicating that the mixtures suitable for microbe media and biofertilizer formula.Abstrak Penggunaan arang hayati (biochar) merupakan alternatif pengelolaan tanah terutama sebagai penyedia karbon dan pembenah tanah.  Kemampuan biochar dalam meningkatkan kesuburan tanah berhubungan dengan kemampuannya untuk menahan air, mengurangi keasaman tanah, menjaga keter-sediaan nutrien yang penting bagi tanaman sehingga mening-katkan  produktivitas  tanaman, serta mengurangi resiko erosi  tanah. Arang hayati  juga berperan dalam menyediakan ling-kungan yang   cocok   untuk   pertumbuhan   mikroba,  ter-masuk isolat Trichoderma harzianum yang digunakan dalam penelitian ini dan teruji mampu meningkatkan pertumbuhan tanaman dan mengendalikan penyakit tular tanah. Tujuan penelitian ini untuk mengetahui kompatibilitas T. harzianum DT38 koleksi BPBPI pada bahan pembawa berupa campuran biochar tandan kosong kelapa sawit (TKKS) dan gambut selama penyimpanan 28 hari secara in vitro. Penelitian ini menggunakan rancangan acak lengkap (RAL) untuk menguji lima perlakuan, yaitu : 1) 100% biochar TKKS (K1), 2) 100% gambut (K2), 3) Campuran biochar TKKS dan gambut 1 : 4 (F1), 4) Campuran biochar TKKS dan gambut 1 : 8 (F2), dan 5) Campuran biochar TKKS dan gambut 1 : 12 (F3). Hasil pengamatan pada penyimpanan 0 dan 7 hari menunjukkan bahwa jumlah propagul T. harzianum DT38 dari berbagai formula tidak berbeda nyata.  Jumlah propagul antara formula F1 dan K2, serta F2 dan F3 tidak berbeda nyata pada penyim-panan 14, 21 dan 28 hari.  Penambahan gambut pada biochar TKKS dapat meningkatkan jumlah propagul T. harzianum DT 38 selama penyimpanan 28 hari secara in vitro.  Jumlah propagul T. harzianum DT38 pada media F1, F2 dan F3 selama penyimpanan 28 hari masih memenuhi jumlah minimal propagul dalam bahan pembawa yang menunjukkan bahwa media ini sesuai untuk pertumbuhan mikroba dan berpotensi sebagai formula pupuk hayati.
Daya hidup planlet karet asal in vitro microcutting pada berbagai periode penutupan sungkup plastik dan komposisi media tumbuh Survival rate of in vitro microcutting-derived rubber plantlets on various plastic cover closed periods and medium compositions . SUMARYONO; Masna Maya SINTA; . NURHAIMI-HARIS
E-Journal Menara Perkebunan Vol 80, No 1: Juni 2012
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (319.119 KB) | DOI: 10.22302/iribb.jur.mp.v80i1.46

Abstract

AbstractIn vitro culture through microcutting technology can be used for clonal propagation of rubber (Hevea brasiliensis Muell. Arg.) rootstocks. Acclimatization of in vitro plantlets to ex vitro conditions is a major bottleneck in the micropropagation of many plants.This research was conducted to study the effect of plastic cover closed period and media composition on the survival rate of rubber plantlets. Plantlets derived from microcutting were planted on plastic pots containing a mixture of soil, cocopeat, dung manure, and sand or zeolite. The plantlets were then placed inside a closed transparent plastic cover that opened after 2, 3, 4 and 6 weeks. The cover was placed under tree canopy. The second experiment used the same media composition with or without cocopeat and with sand or zeolite. At 1.5 month after culture, observation was done on the number of survived plantlets, plantlet height and the percentage of rooted plantlets. The results show that the best coverclosed period was six weeks and the best growing medium was a mixture of soil, cocopeat, dung manure, and zeolite (6:2:1:1v/v). On the two combined treatments, the survival rate was 73.3% after 1.5 month of acclimatization. The use of zeolite and a higher soil percentage gave positive influences on rubber plantlet survival rate. The second experiment results confirmed that the use of zeolite was better than sand and the use of cocopeat was definitely needed. It can be concluded that the best of acclimatization of rubber plantlets from microcutting was on a medium mixture of soil, cocopeat, dung manure, and zeolite (6:2:1:1) and placed inside a closed plastic cover for six weeks before the cover was opened gradually. AbstrakKultur in vitro melalui teknologi microcutting dapat digunakan untuk perbanyakan klonal batang bawah tanaman karet (Hevea brasiliensis Muell. Arg.). Aklimatisasi planlet in vitro ke kondisi ex vitro merupakan hambatan utama pada mikropropagasi berbagai jenis tanaman. Penelitian ini dilakukan untuk mempelajari pengaruh lama penutupan sungkup plastik dan komposisi media tumbuh terhadap daya hidup planlet karet. Planlet karet asal microcutting ditanam pada pot plastik berisi media dengan berbagai campuran tanah, cocopeat, pupuk kandang, dan pasir atau zeolit. Planlet selanjutnya diletakkan di dalam sungkup plastik transparan tertutup rapat yang dibuka setelah 2, 3, 4 dan 6 minggu. Sungkup plastik diletakkan di bawah tajuk pepohonan. Percobaan kedua menggunakan komposisi media serupa dengan atau tanpa cocopeat dan dengan pasir atau zeolit. Pada umur 1,5 bulan, pengamatan dilakukan terhadap jumlah planlet yang hidup, tinggi planlet, dan persentase planlet yang berakar. Hasil penelitian menunjukkan bahwa lama penyungkupan terbaik adalah enam minggu dan media tumbuh terbaik adalah campuran tanah, cocopeat, pupuk kandang, dan zeolit (6:2:1:1 v/v). Pada kombinasi kedua perlakuan tersebut, daya hidup planlet karet mencapai 73,3% setelah 1,5 bulan aklimatisasi. Penggunaan zeolit dan persentase tanah yang lebih tinggi berpengaruh positif terhadap daya hidup planlet karet. Hasil percobaan kedua menegaskan bahwa penggunaan zeolit lebih baik daripada pasir dan penggunaan cocopeat mutlak diperlukan. Dapat disimpulkan bahwa aklimatisasi planlet karet asal microcutting terbaik dilakukan pada media campuran tanah, cocopeat, pupuk kandang, zeolit (6:2:1:1) dan diletakkan di dalam sungkup plastik tertutup selama enam minggu sebelum sungkup dibuka secara bertahap.
Efektivitas dolomit teraktivasi yang diperkaya dengan bakteri pelarut fosfat sebagai pengganti kiserit pada bibit kakao The effectiveness of activated dolomite enriched by phosphate solubilizing bacteria as kieserite substitute on cocoa seedling Laksmita Prima SANTI; Didiek Hadjar GOENADI
E-Journal Menara Perkebunan Vol 80, No 1: Juni 2012
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (140.178 KB) | DOI: 10.22302/iribb.jur.mp.v80i1.40

Abstract

Abstract Magnesium (Mg) deficiency is commonly found in acid soils with high weathering intensity as widely present in tropical and sub-tropical regions, or those developed from low Mg-content parent materials. To overcome Mg deficiency, dolomite is often used to replace kieserite although the former is less reactive than the later. An activation technology by heating up to 800oC, followed by sulfic acid addition, then enriched by phosphate solubilizing bacteria is prospective to improve Mg solubility in soils. This research was aimed to enhance dolomite reactivity and to determine the effectiveness of activated dolomite enriched by phosphate solubilizing bacteria as Mg nutrient sources substituting kieserite on cocoa seedling growth. The results indicate that total and solubility in water of MgO from the prototype of activated dolomite were 26.7 and 9.2%, respectively. Using cocoa seedling as test plant, the use of activated dolomite enriched by using 109 cfu of Pseudomonas sp. at 3.85 g/seedling and combined with 100% dosages of NPK fertilizers showed the best vegetative growth and total dry mass of seedlings was significantly higher than that of 100% NPK-Mg kieserite standard dosage Abstrak Defisiensi Mg umumnya ditemukan pada tanah masam dengan tingkat pelapukan tinggi yang banyak terdapat di daerah tropik, subtropik, dan tanah yang terbentuk dari bahan induk miskin Mg. Untuk mengatasi defisiensi Mg, dolomit sering digunakan sebagai pengganti kiserit walaupun sifatnya kurang reaktif jika dibandingkan kiserit. Teknologi aktivasi dengan pemanasan mencapai 800oC, dilanjutkan dengan penambahan asam sulfat serta pengkayaan dengan bakteri pelarut fosfat diharapkan dapat meningkatkan kelarutan Mg di dalam tanah. Penelitian ini bertujuan untuk meningkatkan reaktivitas dolomit serta menetapkan efektivitas dolomit teraktivasi yang diperkaya dengan bakteri pelarut fosfat sebagai sumber hara Mg pengganti kieserit pada bibit kakao. Hasil yang diperoleh dari penelitian ini mengindikasikan bahwa kadar MgO total dan kelarutan dalam air pada dolomit teraktivasi masing-masing 26,7 dan 9,2%. Dengan menggunakan bibit kakao sebagai tanaman uji, aplikasi 3,85 g dolomit teraktivasi yang diperkaya dengan 109 cfu Pseudomonas sp./bibit yang dikombinasikan dengan 100% dosis pupuk NPK menunjukkan pertumbuhan vegetatif paling baik dan total bobot kering bibit kakao yang secara nyata lebih tinggi jika dibandingkan dengan pemberian 100% dosis standar NPK-Mg kiserit. 
Kloning parsial gen penyandi P5CS dari tebu (Saccharum officinarum L.) Cloning of P5CS-encoding gene fragment from sugarcane (Saccharum officinarum L.) Hayati MINARSIH; . SUPRIYADI; Soekarno Mismana PUTRA; Asmini BUDIANI
E-Journal Menara Perkebunan Vol 80, No 1: Juni 2012
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (364.968 KB) | DOI: 10.22302/iribb.jur.mp.v80i1.48

Abstract

AbstractAbiotic stress such as drought stress is one of the important factors that affect plant growth. Plants have an adaptation mechanism to overcome the stress condition by accumulating osmoprotectant compounds. Proline is a well known compatible solute and can be accumulated to a high concentration in plant cells under drought or osmotic stress. One of the important enzymes in proline biosynthesis is ∆1 - pyrroline-5-carboxylate synthetase (P5CS) encoded by P5CS gene. This research is aimed to clone partial length of P5CS gene from S. officinarum, variety PSJT 941. The amplification of P5CS gene fragment was done by Reverse Transcription-Polymerase Chain Reaction (RT-PCR), using specific primers. DNA fragment of 984 bp, 975 bp and 1725 bp were cloned into Escherichia coli XL1-Blue using pGEMT Easy plasmid vector. Results from BLAST analysis showed that the P5CS sequences have high homology (99%) with the P5CS gene of S. officinarum in the GenBank database. AbstrakCekaman abiotik seperti kekeringan merupakan salah satu faktor penting yang mempengaruhi pertumbuhan tanaman. Tanaman mempunyai strategi adaptasi dalam mengatasi cekaman tersebut dengan mengakumulasi senyawa osmoprotektan yang terakumulasi dalam konsentrasi tinggi. Prolin merupakan salah satu senyawa osmoprotektan yang dapat melindungi tanaman dari cekaman kekeringan maupun osmotik. Salah satu enzim yang berperan penting dalam biosintesis prolin adalah ∆1 -pyrroline-5- carboxylate synthetase (P5CS) yang disandi oleh gen P5CS. Penelitian ini bertujuan untuk mengklon fragmen gen P5CS dari S. officinarum varietas PSJT 941. Amplifikasi fragmen gen P5CS dilakukan dengan teknik Reverse TranscriptionPolymerase Chain Reaction (RT-PCR) menggunakan primer spesifik gen P5CS. Fragmen DNA hasil RT-PCR berukuran 984 bp, 975 bp, dan 1725 bp diklon ke dalam Escherichia coli XL 1-Blue menggunakan vektor plasmid pGEM-T Easy. Hasil analisis BLAST menunjukkan bahwa sekuen fragmen gen produk RT-PCR yang berasal dari S. officinarum PSJT 941 memiliki homologi yang sangat tinggi (99%) dengan gen P5CS pada S. officinarum yang ada dalam pusat data Genbank. 
Perangkat serologi untuk deteksi dini infeksi Ganoderma sp. pada kelapa sawit Serological device kit for early detection of Ganoderma sp. infection in oil palm . SUHARYANTO; Deden Dewantara ERIS; Haryo Tejo PRAKOSO; A H SARAGIH; T W DARMONO
E-Journal Menara Perkebunan Vol 80, No 1: Juni 2012
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (210.644 KB) | DOI: 10.22302/iribb.jur.mp.v80i1.42

Abstract

AbstractBasal stem rot caused by Ganoderma sp. is the most destructive disease in oil palm that difficult to control because its early symptom could not be detected easily. Serological technique that could detect early Ganoderma sp. infection in quick, simple, and cheap manner should be developed as one component for integrated disease management. A diagnostic device based on dot immunobinding assay (DIBA) for early detection of Ganoderma sp. infection in oil palm had been observed at laboratory, greenhouse and field experiment. Study result revealed that serological technique could detect antigen protein extract of Ganoderma mycelium as much as 138 µg/mL. Basal stem of young seedling that artificially be inoculated by the pathogen could also be clearly detected. At field experiment, Ganoderma sp. infection in oil palm plantation was marked with colour marking based on its infection stadium level to the palm oil. The colours are green, yellow, red, black, and white stating that the plant are healthy, mild infection, heavy infection, very heavy infection, and dead, respectively. Field experiment result showed that serological device kit gave strong reaction to antigen extracted from root and stem at red marking plant. The antigen extracted from healthy plant (green marking plant) was the weak one indicating that the plant is starting to be infected although the symptoms are not yet visually observed. AbstrakBusuk pangkal batang (BPB) yang disebabkan oleh Ganoderma sp. merupakan penyakit paling penting yang sulit ditanggulangi pada tanaman kelapa sawit karena gejala dini serangan sulit diketahui. Teknik serologi yang mampu mendeteksi dini infeksi Ganoderma sp. secara cepat, sederhana dan murah perlu dikembangkan sebagai salah satu komponen dalam pengelolaan penyakit secara terpadu. Teknik serologi dalam bentuk perangkat diagnostik berbasis dot immunobinding assay (DIBA) telah dirakit untuk mendeteksi infeksi Ganoderma sp. pada skala laboratorium, rumah kaca, dan lapang. Hasil pengujian menunjukkan bahwa perangkat diagnostik tersebut dapat mendeteksi ekstrak protein dari miselium Ganoderma sp sebesar 138 µg/mL. Keberadaan patogen pada bibit kelapa sawit yang diinfeksi buatan dapat dideteksi secara jelas dengan perangkat serologi tersebut. Deteksi tingkat infeksi Ganoderma sp. pada kebun kelapa sawit TM (skala lapang) dilakukan dengan mengambil sampel berdasarkan stadium infeksi (sehat, ringan, berat, sangat berat, mati) yang diberi kriteria warna hijau, kuning, merah, hitam, dan putih. Hasil uji di kebun kelapa sawit menunjukkan bahwa teknik serologi ini memberikan reaksi paling kuat terhadap antigen yang diekstraksi dari akar dan batang tanaman kriteria merah. Sedangkan reaksi paling lemah ditunjukkan oleh antigen yang diekstraksi dari tanaman kelapa sawit kode hijau yang mengindikasikan bahwa tanaman tanaman kelapa sawit di lapangan tersebut mulai terserang walaupun gejala penyakit belum terlihat secara visual.

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