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Menara Perkebunan
Published by Pusat Penelitian Kelapa Sawit
ISSN : 01259318     EISSN : 18583768     DOI : -
Core Subject : Agriculture,
Agriculture, Biological Sciences & Forestry
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.
Arjuna Subject : -
Articles 541 Documents
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Pupuk organo-kimia untuk pemupukan bibit kelapa sawit Organo-chemical fertilizer for oil palm seedling fertilization Laksmita Prima SANTI; Didiek Hadjar GOENADI
Menara Perkebunan Vol. 76 No. 1: 76 (1), 2008
Publisher : INDONESIAN OIL PALM RESEARCH INSTITUTE

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22302/iribb.jur.mp.v76i1.94

Abstract

SummaryThe availability of high quality and quantity of oil palm seedling needs consistent support of fertilization programs for economic production.  Organo-chemical fertilizer with rock phosphate and urea added was initiated to increased economic value of agriculture and estate crops residues. The prototype of organo-chemical fertilizer has 10% organic C, 11% N, 8% P, 1% K and 4% humic acid respectively. Based on greenhouse experiments, organo-chemical fertilizer treated to oil palm seedlings tends to provide a better vegetative growth of the seedlings.  Dry weights of leave, stem, and root of the seedlings applied with 100 g organo-chemical  fertilizer plus 10 g KCl to each seedling were significantly different compared to the standard dosage conventional fertilizer. This organo-chemical fertilizer could be applied as conventional fertilizer substitute.Ringkasan        Ketersediaan bibit kelapa sawit ber-kualitas dengan kuantitas yang terus meningkat memerlukan dukungan program pemupukan yang konsisten untuk mencapai tingkat produksi yang ekonomis.  Pembuatan pupuk organo-kimia dengan penambahan  batuan fosfat dan N ditujukan untuk meningkatkan nilai ekonomi limbah pertanian dan perkebunan.  Prototipe pupuk organo-kimia ini mengandung 10% C-organik, 11% N, 8% P, 1% K dan 4% asam humik.  Pemberian 100 g pupuk organo-kimia yang ditambah 10 g KCl per bibit menghasilkan berat kering daun, batang, dan akar yang lebih baik dan berbeda nyata apabila dibandingkan dengan peng-gunaan pupuk konvensional dosis standar.  Berdasarkan hasil tersebut, prototipe pupuk organo-kimia ini dapat digunakan sebagai substitusi pupuk konvensional untuk pemupuk-an bibit kelapa sawit.    
Pola aktivitas enzim ligninolitik Pleurotus ostreatus pada limbah sludge pabrik kertas Activity pattern of ligninolytic enzyme of Pleurotus ostreatus in sludge waste of paper factory Happy WIDIASTUTI; . TRI-PANJI
Menara Perkebunan Vol. 76 No. 1: 76 (1), 2008
Publisher : INDONESIAN OIL PALM RESEARCH INSTITUTE

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22302/iribb.jur.mp.v76i1.95

Abstract

Summary Sludge is a solid waste abundantly available on paper factory that is economically unutilized and tends to pollute environment. This waste can be used as growth media for oyster mushroom (Pleurotus ostreatus) as edible mushroom and ligninolytic enzymes production as well. A research has been conducted to study the activity pattern of ligninolytic enzymes of oyster mushroom grown on the sludge waste of recycle paper factory. Six treatments were examinated consisted of three media combinations (sawdust, sludge, sludge mixed with sawdust), with and without supplementing with rice bran, lime, and gypsum, and two mushroom strains Bogor oyster mushroom (JTB) and China Taipei oyster mushroom (JTT). Monitoring of ligninolytic enzyme activity consisting of laccase, mangan peroxidase (Mn-P) and lignin peroxidase (Li-P),  was subsequently regularly started since inoculation, at vegetative phase (four and six weeks), primordial formation, phase of fruiting body formation, and two weeks after formation of fruiting body. Each treatment was repeated three times, so that 216 bag logs of oyster mushroom cultures were performed. The results showed that laccase, Mn-P, and Li-P activities could be observed on sludge or mixture of sludge+sawdust media inoculated with P. ostreatus. Generally, the highest activity of ligninolytic enzymes especially for laccase and MnP were observed at the first vegetative growth phase i.e. before emerging primordial of fruiting body (1.697 & 2.113 U/mL, 4.394 & 2.314 U/mL  respectively for JTB and JTT laccase and JTB & JTT Mn-P). The highest Li-P activity was affected by the kind of media and strain of inoculum. In sludge medium, the highest Li-P activity was observed in  vegetative growth phase (2.706 & 4.014 U/mL respectively for JTB and JTT) while in a mixture of sludge + sawdust the highest activity of that enzyme was observed in primordial phase of growth (2.509 & 1.9 U/mL respectively for JTB and JTT). Addition of supplement to the sludge increased ligninolytic activity, while laccase activity of sludge was suggested could be more enhanced by mixing the sludge with sawdust and enrich with rice bran, gypsum and lime. Ringkasan                                                Sludge merupakan limbah padat yang tersedia melimpah di pabrik kertas dan belum dimanfaatkan secara ekonomis sehingga berpotensi mencemari lingkungan. Limbah ini dapat dimanfaatkan sebagai medium tumbuh jamur konsumsi seperti jamur tiram (Pleurotus ostreatus) dan penghasil enzim ligninolitik. Penelitian dilakukan untuk mempelajari pola aktivitas enzim ligninolitik jamur tiram pada limbah sludge pabrik kertas selama fase vegetatif sampai setelah fase generatif. Enam perlakuan yang diuji berupa tiga kombinasi komposisi medium (serbuk gergaji, sludge, campuran sludge dan serbuk gergaji), dengan dan tanpa pengayaan, yaitu penambahan dedak, kapur, dan gipsum,  serta dua strain jamur tiram Bogor (JTB) dan jamur tiram China Taipei (JTT). Pengamatan aktivitas enzim ligninolitik meliputi lakase, mangan peroksidase (Mn-P) dan lignin peroksidase  (Li-P) dilakukan sejak saat inokulasi, pada fase vegetatif (empat dan enam minggu), pada saat pembentukan primordia, fase tubuh buah, dan dua minggu setelah pembentukan tubuh buah. Masing-masing perlakuan diulang tiga kali sehingga terdapat 216 bag log jamur tiram. Hasil penelitian menunjukkan bahwa aktivitas ligninolitik dijumpai pada medium sludge dan campuran sludge+serbuk gergaji yang diino-kulasi P. ostreatus. Aktivitas enzim ligninolitik tertinggi khususnya lakase dan MnP teramati pada fase pertumbuhan vegetatif pertama yaitu sebelum terbentuknya primordia (1,697 & 2,113 U/mL, 4,394 & 2,314 U/mL  masing-masing untuk lakase JTB dan JTT dan MnP  JTB & JTT). Aktivitas LiP tertinggi dipengaruhi oleh jenis medium dan strain inokulum. Pada medium sludge, aktivitas LiP tertinggi dijumpai pada fase vegetatif (2,706 & 4,014 U/ml masing-masing untuk JTB dan JTT) sedangkan pada medium campuran sludge+serbuk gergaji, aktivitas enzim  ter-tinggi dijumpai  pada fase primordia (2,509 & 1,9 U/ml berturut-turut untuk JTB dan JTT). Pengayaan sludge meningkatkan aktivitas ligninolitik, sedangkan aktivitas lakase pada sludge diduga dapat lebih ditingkatkan dengan menambahkan serbuk gergaji disertai pengayaan berupa gipsum, dedak, dan kapur.
Pengaruh bahan pra-sterilan, tutup tabung kultur, dan musim terhadap tingkat kontaminasi eksplan pada kultur microcutting karet Effect of pre-sterilization agent, culture tube closure, and season on the contamination level of rubber microcutting culture . NURHAIMI-HARIS; . SUMARYONO; M.P. CARRON CARRON
Menara Perkebunan Vol. 77 No. 2: 77 (2), 2009
Publisher : INDONESIAN OIL PALM RESEARCH INSTITUTE

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22302/iribb.jur.mp.v77i2.96

Abstract

AbstractMicrobial contamination is a major obstaclein clonal propagation of hevea (Heveabrasiliensis) through microcutting technology;therefore the ability to reduce contamination willdetermine the success of the application of thistechnology. The aim of experiments was toincrease healthy and survived plantlets by testingpre-sterilization agents for cleaning explantsduring pre-sterilization step, culture tubeclosures suitable for explants growth and anappropriate time for introducing explants at theprimary culture phase. The pre-sterilizationagents tested were aganol, alcohol anddesogerme, the culture tube closures used wereparafilm and cotton, and the time for culturingexplants were determined by using rubbergenotypes introduced during the year of 2006 and2007. The results show that desogermedecreased significantly the level of explantcontamination compared to aganol and alcohol,meanwhile the type of culture tube closure didnot affect the level of explant contamination. Thetype of culture tube closure influencedsignificantly the survival of explants where thenumber of survived explants in culture tubescovered with cotton was higher than that of withparafilm. Season also affected the contaminationfrequency of the explants. Higher number ofhealthy plantlets were obtained whenintroduction of the explants were conducted fromJune to October considered as dry season inBogor compared to introduction of the explantsduring rainy season from January to May.Different genotypes of rubber introduced at theprimary culture phase did not affect thepercentage of explant contamination.AbstrakKontaminasi oleh mikroba merupakanmasalah utama pada perbanyakan klonal tanamankaret (Hevea brasiliensis) melalui teknologimicrocutting sehingga kemampuan mengurangikontaminasi menentukan keberhasilan aplikasiteknologi tersebut. Penelitian ini bertujuanmempelajari pengaruh jenis bahan pra-sterilanyang efektif untuk pencucian eksplan tahap pra-sterilisasi, mempelajari pengaruh tutup tabungterhadap perkembangan eksplan serta meng-identifikasi waktu yang tepat untuk melaksanakanintroduksi eksplan pada tahap kultur primer(kultur awal) sehingga jumlah eksplan sehat dantumbuh dapat ditingkatkan. Bahan pra- sterilanyang diuji adalah aganol, alkohol dan desogerme,tutup tabung yang digunakan adalah parafilm dankapas, sedangkan identifikasi waktu kulturdilakukan melalui introduksi eksplan sepanjang tahun 2006 dan 2007 terhadap berbagai genotipetanaman karet yang tersedia. Hasil penelitianmenunjukkan bahwa desogerme menurunkansecara nyata tingkat kontaminasi eksplandibandingkan dengan aganol dan alkohol,sedangkan jenis tutup tabung tidak berpengaruhterhadap persentase kontaminasi. Jenis tutuptabung berpengaruh sangat nyata terhadappersentase eksplan yang hidup dan membentuktunas, di mana persentase eksplan membentuktunas pada tabung dengan tutup kapas lebih tinggidibandingkan dengan tutup parafilm. Musim jugasangat mempengaruhi tingkat kontaminasieksplan. Eksplan sehat jauh lebih banyakdiperoleh apabila penanaman eksplan dilakukanpada bulan Juni sampai Oktober, yang merupakanmusim kemarau di Bogor dibandingkan denganintroduksi eksplan pada bulan Januari sampaiMei, yang merupakan musim hujan. Jenisgenotipe yang ditanam pada tahap kultur primertidak berpengaruh terhadap persentasekontaminasi.
Pengaruh interval dan lama perendaman terhadap pertumbuhan dan pendewasaan embrio somatik tanaman sagu (Metroxylon sagu Rottb.) Effect of immersion interval and duration on the growth and maturation of somatic embryos of sago palm ( Metroxylon sagu Rottb.) Imron RIYADI; . SUMARYON
Menara Perkebunan Vol. 77 No. 2: 77 (2), 2009
Publisher : INDONESIAN OIL PALM RESEARCH INSTITUTE

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22302/iribb.jur.mp.v77i2.97

Abstract

AbstractLiquid culture via temporary immersionsystem (TIS) has a potency for enhancingmaturity and uniformity of plant somatic embryos(SE). An experiment was conducted to determinethe effect of medium immersion interval andduration on the growth and maturation of sagoSE in TIS. A clump of SE at globular stagederived from sucker’s tip meristem culture wasused as material source. The SE were cultured ona modified Murashige and Skoog medium addedwith 0.01 mg/L ABA, 1.0 mg/L kinetin and0.1 mg/L GA 3 . The treatments used were TISwith immersion interval of 3, 6 and 12 hourswith duration of 1 and 3 minutes. Solid mediumwas used as a control. The results show that TISwith immersion interval 12 hours for threeminutes produced the highest SE biomass(14.6 g/flask) which had increased by 9.8-foldwithin six weeks. The longer of immersioninterval (less frequent) and the longer ofimmersion duration (three minutes) increasedsignificantly biomass fresh weight of of sago SE.SE biomass of sago on solid medium wassignificantly lower than those of in liquid mediaof TIS. The highest number of advanced stageembryos (torpedo, cotyledonary and earlygerminant) of 643 or 48.2% from the totalnumber of SE was achieved in TIS with 12 hoursinterval for three minutes. During the maturationof sago SE, the color of embryos has changedfrom mostly yellowish to greenish and reddish.AbstrakKultur cair dengan sistem perendaman sesaat(SPS) berpotensi untuk meningkatkanpendewasaan dan keseragaman embrio somatik(ES) tanaman. Penelitian ini bertujuan untukmenentukan pengaruh interval dan lamaperendaman terhadap proses pendewasaan ESsagu dalam SPS. Bahan yang digunakan berupaES fase globuler asal kultur pucuk tunas anakansagu. ES sagu dikulturkan dalam mediumMurashige dan Skoog yang dimodifikasiditambah ABA 0,01 mg/L; kinetin 1 mg/L danGA 3 0,1 mg/L. Perlakuan yang digunakan adalahkultur SPS dengan interval perendaman 3, 6 dan12 jam dengan lama perendaman 1 dan 3 menitserta kultur padat sebagai pembanding. Hasilpenelitian menunjukkan bahwa perlakuan SPSdengan interval perendaman 12 jam selama tigamenit menghasilkan bobot biomassa ES tertinggiyaitu 14,6 g/bejana yang meningkat 9,8 kalidalam waktu enam minggu. Interval peren-daman lebih lama (lebih jarang) dan lama peren-daman lebih panjang (tiga menit) meningkatkansecara nyata bobot segar biomassa ES sagu.Biomassa ES sagu pada medium padat secaranyata lebih rendah dibandingkan dengan kulturkotiledon dan kecambah dini) tertinggi yaitu 643atau 48,2% dari jumlah total ES diperoleh pada perlakuan SPS interval 12 jam dengan lama tigamenit. Seiring dengan pendewasaan ES sagu, terjadi perubahan warna dari sebagian besar kuning menjadi hijau dan merah.
Potensi Pseudomonas fluorescens strain KTSS untuk bioremediasi merkuri di dalam tanah The Potential use of Pseudomonas fluorescens KTSS strain formercury bioremediation in the soil Laksmita Prima SANTI; Didiek Hadjar GOENADI
Menara Perkebunan Vol. 77 No. 2: 77 (2), 2009
Publisher : INDONESIAN OIL PALM RESEARCH INSTITUTE

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22302/iribb.jur.mp.v77i2.100

Abstract

AbstractHeavy metals are widespread pollutants insoil and become environmental concern as theyare non-degradable and highly persistent. Solidand/or liquid wastes containing toxic heavymetals may be generated in various industrial ormining processes. A heavy metal resistantbacterium may be present in the soil and miningsite. As they already preconditioned by abundantheavy metals contaminant, the use of thesebacterium is assumed to be effective in improvingmetals reduction. To obtain bacterial isolateshighly capable of mercury (Hg) reduction,isolation activities have been conducted atselected sites of mining locations in SouthSumatera. The highly potential bacteriapossessing mercury reducing capability has beenisolated from this site i.e. Pseudomonasfluorescens KTSS strain. Inoculating of 25%(v/w) suspension of P. fluorescens KTSS strain insoil material added 5000 ppb of mercury, couldreduced about 53.3% of mercury soil contents.Best vegetative growth performance of cocoaseedlings was shown by the application of 15-15-15 NPK conventional fertilizers in combinationwith the addition of 1.6 – 3.25 g of P. fluorescensKTSS bio-ameliorant/seed. A Greenhouseexperiment results of cocoa seedlings were inconcordance with those obtained from field trialsof paddy.AbstrakLogam berat merupakan jenis polutan yangterdistribusi secara luas di dalam tanah danmendapat perhatian secara khusus karena sifatnyayang tidak dapat terdegradasi serta dapat bertahanlama di dalam lingkungan. Limbah padatdan/atau cair yang dihasilkan dari berbagai prosesindustri dan pertambangan mengandung logamberat toksik. Jenis bakteri yang resisten terhadaplogam berat mungkin berada di dalam tanah dandi lokasi tambang. Apabila bakteri tersebut dapatberadaptasi pada lingkungan dengan tingkatkontaminasi logam berat yang tinggi, makadiasumsikan bahwa penggunaan bakteri tersebutsangat efektif dalam meningkatkan reduksi logamberat. Untuk memperoleh isolat bakteri yangmemiliki kemampuan mereduksi merkuri (Hg),maka satu rangkaian kegiatan isolasi telahdilakukan di lokasi tambang terpilih di SumateraSelatan. Bakteri potensial pereduksi merkuri yangtelah diisolasi dari lokasi ini diidentifikasisebagai Pseudomonas fluorescens strain KTSS.Inokulasi sebanyak 25% (v/b) suspensi P. fluore-scens strain KTSS ke dalam bahan tanah yangtelah ditambah dengan 5000 ppb merkuri, dapatmereduksi sekitar 53,3% kandungan merkuri didalam tanah. Pertumbuhan terbaik dari bibitkakao diperoleh dari perlakuan pupuk NPK 15-15-15 yang dikombinasikan dengan 1,6 – 3,25 gbioamelioran P. Fluorescens strain KTSS/bibit.Pengujian bioamelioran P. fluorescens strainKTSS di lapang pada tanaman padi memberikanpola keefektifan yang sama dengan hasilpengujian terhadap bibit kakao yang dilakukan dirumah kaca.
Kloning gen LEAFY kakao dari jaringan bantalan bunga aktif Cloning of cacao LEAFY gene from the active flower cushions Tetty CHAIDAMSARI; Rita HAYATI; Auzar SYARIEF; Aswaldi ANWAR; Djoko SANTOSO
Menara Perkebunan Vol. 77 No. 2: 77 (2), 2009
Publisher : INDONESIAN OIL PALM RESEARCH INSTITUTE

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22302/iribb.jur.mp.v77i2.179

Abstract

SummaryAttempts to improve productivity of cacaoplantations lead us to study the molecularmechanism of flowering. In the model speciesArabidopsis thaliana as well as some otherspecies, LEAFY is a central regulatory gene forthe transition of shoot apical meristems toflowering meristems. Different from that ofArabidopsis, cacao inflorescence is acauliflorous type, by which flowers can developrepeatedly from the same flower cushion on thetrunk. In this research, a LEAFY homolog wasisolated from active flower cushion with RT-PCRusing a pair of DNA primer specifically designedto isolate its complete cds. Gel electrophoresisexamination indicated the presence of a 1.2 kbamplicon. Purified from the gel, this DNAfragment was cloned into competent cells ofE. coli XL1 Blue using pGEM-T Easy cloningvector at an orientation according to the T7promoter of the plasmid. Sequence analysis usingBLASTX, showed that the amplicon was LEAFY(LFY) homolog. Alignment analysis using ClustalW indicated that the cTcLFY highly homologousto those from other perennial crops such ascitrus, grape, apple and poplar. The highesthomology (conserved region) was found in the Cterminal of the encoded proteins.RingkasanUsaha untuk meningkatkan produktivitasperkebunan kakao telah mendorong penelitianmolekuler tentang mekanisme pembungaankakao. Pada tanaman model Arabidopsis thalianadan lainnya, LEAFY merupakan gen kunci dalamtransisi meristem tunas jadi meristem bunga.Berbeda dengan sistem pada Arabidopsis,pembungaan kakao termasuk tipe cauliflorous,bunga dapat muncul dari bantalan bunga yangsama sepanjang tahun. Dalam penelitian inihomolog LFY diisolasi dari bantalan bunga aktifmenggunakan RT-PCR dengan sepasang primerspesifik yang dirancang berdasarkan sekuenDNA di kedua ujung gen tersebut. Pemeriksaangel elektroforesis menunjukkan adanya amplikontunggal berukuran 1,2 kb. Setelah dimurnikandari gel, amplikon dapat diklon ke dalam selkompeten E. coli galur XL1 Blue menggunakanvektor pGEM-T Easy dengan orientasi yangsesuai dengan promoter T7 dari vektor. AnalisisBLASTX sekuen DNA membuktikan bahwaamplikon tersebut adalah homolog dari genLEAFY. Analisis penjajaran dengan mengguna-kan ClustalW menunjukkan bahwa gen cTcLFYtersebut memiliki homologi yang tinggi dengangen sejenis dari tanaman keras lainnya sepertitanaman jeruk, anggur, apel dan poplar.Homologi tertinggi (daerah terkonservasi)terdapat pada ujung (terminal) C dari proteinyang disandinya.
Effect of enzymatic hydrolysis and nitrogen on Saccharomyces cerevisiae β-glucan production from Manihot utilissima and Maranta arunadinacea waste Misri A Gozan; Fita Sefriana; Yemirta Yemirta; Muhammad Arif Darmawan
Menara Perkebunan Vol. 91 No. 1 (2023): 91 (1), 2023
Publisher : INDONESIAN OIL PALM RESEARCH INSTITUTE

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22302/iribb.jur.mp.v91i1.508

Abstract

This experiment utilised cassava (Manihot utillissima) and arrowroot (Maranta arunadinacea) wastes as the medium of propagation of Saccharomyces cerevisiae to produce β-glucan. The amyloglucosidase hydrolysed the waste, followed by fermentation in the nitrogenous medium by S. cerevisiae. The β-glucan pellet was extracted using 2% NaOH alkaline solution at 90°C for 5 hours, followed by a series of centrifugation processes. The highest glucose concentration from hydrolysis resulted from adding 57.5 mg amyloglucosidase enzyme for arrowroot waste with 95.93% conversion and 50 mg enzyme for cassava waste with 64.70% conversion. The highest amount was obtained for producing S. cerevisiae by adding 4.75 g peptone to all samples. The optimum number of cells was obtained at 1.61 x 108 colonies at t = 48 hours for arrowroot waste and 8.55 x 107 colonies at t = 48 hours for cassava waste. For β-glucan production, the highest number was obtained by using 3.99 g of peptone for cassava waste with a yield of 1.20% and by using 4.75 g of peptone for arrowroot waste with a yield of 1.23%. For β-glucan pellet, the highest number was 1.77 g L-1 (0.18 % b/v) from cassava waste medium and 1.91 g L-1 (0.19% b/v) from arrowroot waste. Mutant cells in the Yeast Extract–Peptone–Glycerol (YPG) medium produced 6.56 g L-1 (0.66% b/v) β-glucan pellet, while wild-type cells in the similar medium produced 1.84 g L-1 (0.18% b/v).
Optimasi sistem kultur dan media untuk peningkatan tinggi tunas in vitro kelapa sawit Masna Maya Sinta; Rizka Tamania Saptari; Imron Riyadi; Sumaryono Sumaryono
Menara Perkebunan Vol. 91 No. 1 (2023): 91 (1), 2023
Publisher : INDONESIAN OIL PALM RESEARCH INSTITUTE

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22302/iribb.jur.mp.v91i1.511

Abstract

Optimization of in vitro shoot growth is necessary to shorten the culture time and produce vigorous oil palm plantlets. This research was conducted to determine the best media and culture techniques to accelerate in vitro shoot growth of oil palm. Shoots of oil palm derived from somatic embryogenesis were grown on DF media with two culture systems (solid medium and double-layer) combined with hormone treatments (0.5-1 mg L-1 giberellin/GA3 and 0.5 mg L-1 Benzyl amino purine/BAP or thidiazuron/ TDZ). Further optimization was conducted using different bottle closures (polypropylene screw caps and plastic wraps) and macronutrients (standard or double concentrations). This research was conducted using a completely randomized design (CRD), with each treatment consisting of 5 bottle replications and each bottle consisting of 5 shoots. The results showed that media with double-layer system combined with GA3 (0.5-1 mg L-1) and TDZ (0.5 mg L-1) gave the highest shoot height increment. The use of double-strength macronutrient media combined with screw bottle caps increased shoot height (136-167 %) and decreased shoot tip necrosis (0-24 %). Plastic wrap bottle caps increased shoot tip necrosis (STN), while doubling macronutrients reduced STN. The growth of oil palm shoots began to slow down after 5 weeks of culture. In conclusion, the optimal conditions for in vitro shoot growth of oil palm were at usage of double-layer media added with GA3 0.5-1 mg L-1, TDZ 0.5 mg L-1, and double macronutrients on bottle jars with polypropylene screw caps.
Transformation of DHN1 gene and DHN promoter constructs into sugarcane calli, regeneration of the calli, and acclimatization of the plantlets Hayati Minarsih; Fauziatul Fitriyah; Annisa Aulya Aksa; Turhadi Turhadi; Deden Sukmadjaya; Sustiprajitno Sustiprajitno
Menara Perkebunan Vol. 91 No. 1 (2023): 91 (1), 2023
Publisher : INDONESIAN OIL PALM RESEARCH INSTITUTE

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22302/iribb.jur.mp.v91i1.512

Abstract

Dehydrin is known to have an important role in plant response and adaptation to abiotic stresses including drought and high salinity. Previous research reported the isolation of the full-length coding sequence (CDS) of DHN1 from sugarcane var. PSJT 941, and it shares a high homology with DHN genes from sorghum and other sugarcane varieties. In this study, the full-length CDS was cloned under the constitutive CaMV35S promoter and transformed into sugarcane calli mediated by Agrobacterium tumefaciens. The DHN promoter, Pr-1DHNSo, was also successfully isolated from the sugarcane var. PSJT 941 and cloned into the pBI121 expression vector. The promoter construct was subsequently transformed into sugarcane calli of var. Kidang Kencana. Transgenic sugarcane carrying DHN1 gene and DHN promoter constructs were regenerated according to the standard protocol of sugarcane tissue culture. Optimization of an acclimatization protocol using modified post-rooting media was also conducted and the resulting protocol reduced the total mortality rates of the transformed plantlets. The presence of the gene and promoter constructs was periodically tested by PCR using specific primers. The genotyping results showed that the constructs were present for more than a year after transformation.
Improvement of purification process of stevia extract by combination of microfiltration and ultrafiltration Michael Silaen; Erliza Noor; Mulyorini Rahayuningsih
Menara Perkebunan Vol. 91 No. 1 (2023): 91 (1), 2023
Publisher : INDONESIAN OIL PALM RESEARCH INSTITUTE

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22302/iribb.jur.mp.v91i1.521

Abstract

Microfiltration and ultrafiltration are used for the purification process of stevia extract to retain steviosides and remove tannins. The main objective of this study was to obtain the operating conditions for the purification process of stevia extract that resulted in the lowest stevioside rejection and highest tannin rejection. The purification process of stevia extract using microfiltration membrane was carried out at transmembrane pressure (1.20, 1.40, 1.65, 1.80, and 1.90 bar), cross flow velocity (0.04, 0.06, and 0.11 m s-1), and stevioside concentration of feed (7.12, 10.25, 14.03, and 18.47 g L-1). The stevia extract purification process used ultrafiltration membrane at transmembrane pressure (1.20, 1.40, 1.65, 1.80, and 1.90 bar), cross flow velocity (0.06, 0.09, and 0.12 m s-1), and stevioside concentration of feed (4.59 and 10.36 g L-1). The first step purification process was carried out using a microfiltration membrane and the resulting permeate was used as feed for the ultrafiltration process. The second step purification process was carried out using an ultrafiltration membrane. The best operating conditions of the microfiltration process were feed stevioside concentration of 14.03 g L-1 at a transmembrane pressure of 1.90 bar and a cross flow velocity of 0.11 m s-1 with a permeate flux of 82.90 L m-2 h-1. The best operating conditions of the ultrafiltration process used a feed stevioside concentration of 10.36 g L-1 with a permeate flux of 26.51 L m-2 h-1 at a transmembrane pressure of 1.90 bar and a cross flow velocity of 0.12 m s-1. The microfiltration and ultrafiltration processes resulted in total stevioside rejection of 59.52 % and total tannin rejection of 57.99 %.

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