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All Journal JPTK: Jurnal Pendidikan Teknologi dan Kejuruan Neo-Bis INDONESIAN JOURNAL OF APPLIED PHYSICS Jurnal Dinamika Sosial Budaya Jurnal Riset Ekonomi dan Bisnis Menara Perkebunan Indonesian Journal of Clinical Pathology and Medical Laboratory (IJCPML) Jurnal Ilmiah Edunomika (JIE) SOLUSI Jurnal Tanah dan Iklim Jurnal Bingkai Ekonomi (JBE) Jurnal Pengabdian kepada Masyarakat Indonesia (JPKMI) Jurnal Informasi dan Komunikasi Administrasi (JIKAP) Unisia Sustainable Business Journal

Djoko Santoso

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Author-ID : 255068

Religion Agriculture, Biological Sciences & Forestry Arts Humanities Astronomy Biochemistry, Genetics & Molecular Biology Computer Science & IT Decision Sciences, Operations Research & Management Economics, Econometrics & Finance Education Energy Health Professions Industrial & Manufacturing Engineering Materials Science & Nanotechnology Medicine & Pharmacology Neuroscience Nursing Physics Public Health Social Sciences Other

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The effects of seaweed fertilizer on the growth and productivity of upland rice, maize and oil palm grown in green house Pengaruh pupuk rumput laut terhadap pertumbuhan dan produktivitas padi gogo, jagung dan kelapa sawit di rumah kaca Djoko SANTOSO; Tetty CHAIDAMSARI; . SYAFARUDDIN; Dedi Soleh EFFENDI
E-Journal Menara Perkebunan Vol 79, No 2: Desember 2011
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

AbstrakSebagai negara kepulauan di daerah tropis, Indonesiakaya akan sumberdaya alam untuk swasembada pangan.Berjuta-juta hektar lahan di Indonesia ditanami tanamanperkebunan, tanaman tahunan yang memiliki masa juvenilyang relatif lama, terutama tanaman kelapa sawit dan karet.Sementara itu, upaya untuk meningkatkan produksi panganterkendala oleh terbatasnya lahan subur. Penelitian yangmengeksplorasi bioregulator alami mampu meningkatkanproduktivitas tanaman, menemukan bahwa Sargasum sp.,rumput laut tipe liar yang di sepanjang pantai beberapawilayah Indonesia, menunjukkan kemampuannya meningkat-kan pertumbuhan dan produktivitas tanaman seperti padi,jagung, tomat dan pertumbuhan kelapa sawit tanpapenambahan pupuk kimia. Percobaan pada padi gogovarietas Batutegi yang ditanam di rumah kaca, menunjuk-kan bahwa bioregulator alami tersebut meningkatkanproduktivitasnya 50% lebih tinggi daripada kontrolnya.Percobaan menggunakan jagung var. Arjuna, tanaman yangtelah diperlakukan dengan bioregulator tersebut mem-produksi dua hingga tiga tongkol, sementara pada tanamankontrol hanya satu tongkol. Percobaan pada tanamankelapa sawit di rumahkaca memperlihatkan bahwa bio-regulator tersebut menginduksi pertumbuhan vegetatifnyasecara signifikan, lebih baik daripada kontrol dengan atautanpa pupuk kimia. Intercropping tanaman kelapa sawitTBM dengan tanaman pangan seperti padi gogo ataujagung, diharapkan lebih menguntungkan bagi usahaperkebunan.AbstractBeing a tropical archipelago, Indonesia is rich withnatural resources enabling more production for food.Millions hectares of Indonesian lands is now planted withestate crops, perennial crops with relatively lengthenjuvenile phase mainly oil palm and rubber. Meanwhile,attempts to increase national food production have beenlimited by availability of fertile lands. Our researchexploring natural bioregulator capable of improving cropproductivity, found that Sargasum sp., a wild sea weedgrown mostly along the coast line in Indonesia, indicated itsability to improve the growth and productivity of crops likerice, maize, tomato and oil palm even though with nochemical fertilizers added. The experiment on upland rice oflocal variety Batutegi planted in greenhouse, demonstratedthe natural bioregulator has increased the rice productivityby at least 50% over the control. The experiment usingmaize var. Arjuna, the bioregulator treated plants has madetwo to three corncobs instead of only one corncob on thecontrol plants. The experiment on the oil palm grown in thenursery showed that the bioregulator has significantlyinduced vegetative growth better than the control with orwithout chemical fertilizers. Intercropping the food crops,rice or maize in the juvenile phase of the oil palmplantations, should be beneficial to the productivity of theplantation.

Keragaman sekuen DNA fragmen gen penyandi ACCase subunit BCCP dari tiga tipe kelapa sawit Variability of DNA sequence of gene fragment encoding BCCP subunit of ACCase from three types of oil palm Asmini BUDIANI; Djoko SANTOSO; A.R. PURBA PURBA
E-Journal Menara Perkebunan Vol 75, No 1: Juni 2007
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

SummaryHeteromeric acetyl-CoA carboxylase (ht-ACCase) is one of key enzymes in palm oilbiosynthesis. Isolation and characterization ofthe gene is an important step in metabolicengineering to increase palm oil content andquality. The objective of this research was toisolate DNA fragment of gene encoding biotincarboxyl carrier protein (BCCP) subunit of ht-ACCase from three different oil palm types(Simalungun, Hibrida and Backcross) andinvestigate the variation of its DNA sequence.Total RNA was isolated from the mesocarp ofoil palm. DNA fragment encoding BCCP wasamplified by means of Reverse TranscriptasePolymerase Chain Reaction (RT-PCR) usingspecific primers with total RNA as a template.The products of RT-PCR were then purifiedfrom the gel, cloned and sequenced. The DNAsequences were analyzed for their homologiesto BCCP gene using BlastN and aligned todetect the sequence variability using ClustalWprogram from BioEdit. The results show thatone of the two RT-PCR products at about 300bp was highly homologous with the geneencoding BCCP from Glycine max, Brassicanapus and Arabidopsis thaliana. Nucleotidesequences of that BCCP fragments from thethree types of oil palm displayed some degreesof variability. Further investigation is neededto analyze the variability of the DNA sequencesof the full-length gene in relation with oilcontent or other characterRingkasanAsetil-CoA karboksilase heteromerik (ht-ACCase) merupakan salah satu enzim kuncidalam biosintesis minyak sawit. Isolasi dankarakterisasi gen tersebut merupakan langkahpenting dalam upaya rekayasa metabolismeuntuk peningkatan rendemen dan kualitasminyak sawit. Penelitian ini bertujuan untukmengisolasi fragmen DNA penyandi subunitbiotin carboxyl carrier protein (BCCP) dari ht-ACCase dari tiga tipe kelapa sawit yang ber-beda (Simalungun, Hibrida dan Backcross)dan mempelajari keragaman susunan nukleo-tidanya. RNA total diisolasi dari mesokarpbuah sawit. Fragmen gen penyandi BCCPdiamplifikasi dengan Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR) meng-gunakan primer spesifik dan templat RNA total.Fragmen hasil RT-PCR dimurnikan dari gel,diklon kemudian disekuen. Sekuen DNA yangdiperoleh dianalisis homologinya dengan genBCCP menggunakan BlastN dan disejajarkanuntuk mengetahui keragamannya mengguna-kan program ClustalW dari BioEdit. Hasilnyamenunjukkan bahwa satu dari dua fragmenhasil RT-PCR yang berukuran sekitar 300 pbmemiliki homologi yang tinggi denganfragmen gen penyandi BCCP dari Glycine max,Brassica napus dan Arabidopsis thaliana.Urutan nukleotida fragmen BCCP dari ketigatipe kelapa sawit menunjukkan keragaman.Perlu analisis lebih lanjut mengenai keragamansekuen DNA dari gen lengkapnya dan dikajihubungannya dengan akumulasi minyak ataukarakter lain

Kloning gen penyandi β-1,6-glukanase kapang secara cepat dengan teknik RT-PCR menggunakan primer spesifik Rapid cloning for gene encoding fungal β-1,6-glucanase by means of RT-PCR using specific primers Asmini BUDIANI; Riza A. PUTRANTO; Hayati MINARSIH; Niyyah FITRANTI; Djoko SANTOSO
E-Journal Menara Perkebunan Vol 77, No 1: Juni 2009
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

AbstractProduction of bioethanol from biomass ofagricultural waste has been hindered with a highproduction cost because enzymes needed for theprocess has to be imported with relatively a highprice. Genetic engineering using its encodinggenes is able to produce those enzymes withlower cost. In this report we described a researchaimed to clone gene encoding β-1,6-glucanasefrom Trichoderma harzianum with a relativelyrapid and inexpensive method, by means of RT-PCR using gene specific primers. The primerswere designed based on the DNA sequence of thetarget gene from the same species of organismused in this research. RT-PCR using that primersresulted in DNA fragment with sizescorresponding to the predicted size of full lengthgene encoding β-1,6-glucanase, about 1300 bp.After a sequential experiments of cloning usingpGEM-T Easy vector, DNA sequencing andBlastN - BlastX analyses of the sequences, it wasproven that the isolated DNA was full length geneof β-1,6-glucanase. This was implied from thepercentage of Identity and E-value which were96% and 0.0 (< e-04) respectivety.AbstrakProduksi bioetanol dari biomassa limbahpertanian, terkendala oleh tingginya biayaproduksi karena enzim yang diperlukan untukproses tersebut masih harus diimpor denganharga yang relatif mahal. Melalui rekayasagenetika menggunakan gen-gen penyandinya,enzim-enzim tersebut dapat diproduksi denganbiaya yang lebih murah. Penelitian ini bertujuanuntuk mengklon gen penyandi β-1,6-glukanasedari Trichoderma harzianum secara cepat danekonomis, dengan RT-PCR menggunakan primerspesifik. Primer tersebut dirancang berdasarkansekuen DNA dari gen target asal spesiesorganisme yang sama dengan yang digunakandalam penelitian. RT-PCR dengan primertersebut menghasilkan fragmen DNA yangukurannya sesuai dengan gen lengkap penyandiβ-1,6-glukanase, yaitu sekitar 1300 bp. Setelahsecara berurutan diklon menggunakan vektorpGEM-T Easy, sekuensing urutan DNA dananalisis BlastN maupun BlastX dari sekuen yangdiperoleh, terbukti bahwa fragmen DNA tersebutadalah gen lengkap penyandi β-1,6-glukanase.Hal ini ditunjukkan oleh Nilai Kesamaan(Identity) dan E-Value yang masing-masingmencapai 96% dan 0.0.

Nucleotide sequence of cryIA gene cloned from Btk isolate of Bacillus thuringiensis and comparison with cryIA(c) gene from B. thuringiensis subsp. kenyae Sekuen nukleotida gen cryIA dari B.thuringiensis isolat Btk dibandingkan dengan gen crylA(c) dari B. thuringiensis subsp. Kenyae Asmini BUDIANI; Djoko SANTOSO
E-Journal Menara Perkebunan Vol 68, No 1: Juni 2000
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Ringkasan Perakitan tanaman perkebunan yang toleran terhadap serangga hama dapat ditempuh melalui rekayasa genetika menggunakan gen cry. Gen cryIA merupakan gen cry yang paling banyak dipelajari di antara gen cry lainnya. Berdasarkan homology sekuen dan spesifisitas protein yang disandinya terhadap serangga sasaran, gen ini telah diklasifikasikan menjadi 10 subklas. Tulisan ini melaporkan hasil sekuensing (ragmen gen cryIA penyandi domain toksin yang diisolasi dengan teknik PCR dari Bacillus thuringiensis isolat Btk dan diklon menggunakan vektor pGEMT. Untuk menentukan sekuen gen cryIA yang berukuran sekitar 2 kb tersebut, dilakukan konstruksi satu seri mutan terdelesi searah dari ujung 5' menggunakan kit Erase-a-Base-System. Tiga DNA gen cryIA mutan dengan tingkat delesi yang sesuai dan satu nonmutan dipilih untuk sekuensing DNAnya. Sekuensing dilakukan dari satu arah menggunakan primer universal SP6 pada alat ABI 377A automatic DNA sequencer. Sekuen lengkap dari gen cryIA diperoleh dengan cara menggabungkan sekuen ketiga mutan dengan sekuen dari gen cryIA nonmutan secara manual. Untuk konfirmasi sekuen ujung 3', dilakukan sekuensing dari arah lainnya menggunakan primer universal T7. Sekuen lengkap dari fragmen tersebut mengandung 2021 nukleotida dan menyandi protein dengan 673 asam amino. Dibandingkan dengan sekuen gen crylA(c) dari B. thuringiensis subsp. kenyae, terlihat adanya sepuluh mutasi titik masing-masing pada nukleotida ke 444, 477, 1089, 1092, 1098, 1242, 1566, 1869, 1906 dan 1961. Tujuh mutasi titik pada nukleotida ke 444, 477, 1089, 1092, 1242, 1566, dan 1869 tidak merubah asam amino, sedangkan tiga mutasi lainnya mengakibatkan perubahan asam amino, yaitu pada nukleotida ke 1098 (kodon ke 366, yang menyebabkan perubahan dari Phe menjadi Leu), nukleotida ke 1906 (kodon ke 636, yang mengubah Val menjadi Leu) dan pada nukleotida ke 1961(kodon ke 654, yang mengubah Cys menjadi Tyr).Summary Estate crops tolerant to pests can be development through genetic engineering using cry gene. CryIA is the best studied among cry genes. Based on the sequence homology and specificity of their encoded proteins to the, targeted insect, these genes have been classified into 10 subclasses. This paper reports sequencing of cryIA gene fragment en-coding toxin domain isolated from Btk isolates of Bacillus thuringiensis using PCR technique and cloned with pGEM-T vector. To determine the full sequence of the 2-kb gene fragment, a series of mutants uni-directionally deleted at the 5'-end were constructed. Mutation was done using Erase-a Base-System kit. Three DNA mutants with appropriate degree of deletion and the un-mutated DNA were chosen for sequencing. Sequencing was conducted from one direction with SP6 universal primer using the ABI 377A automatic DNA sequencer. The full sequence of cryIA fragment was assembled manually using the sequences of DNA mutants and the non-mutant cryIA fragment. To confirm the sequence of the 3'-end, sequencing from the other direction was performed using the T7 universal primer.The completed sequence of the fragment contains 2021 nucleotides encoding a protein of 673 amino acids. Compares to the sequence of cryIA(c) from B. thuringiensis subsp. kenyae, it was shown that there were ten point mutations (nucleotides of 444, 477, 1089, 1092, 1098, 1242, 1566, 1869, 1906 and 1961), sevent of them (nucleotides of 444, 477, 1089, 1092, 1242, 1566 and 1869) were identified as silent mutations, while the other three substituted the amino acids, which are at the nucleotide 1089 (codon 366, substitution of Leu for Phe), nucleotide 1906 (codon 636, substitution of Leu for Val), and nucleotide 1961 (codon 654, substitution of Tyr for Cys).

Kloning dan karakterisasi gen penyandi inhibitor proteinase dari kulit buah kakao Cloning and characterization of gene encoding proteinase inhibitor of cacao pod wall Mayta Novaliza ISDA; Musliar KASIM; . MANSYURDIN; Tetty CHAIDAMSARI; Djoko SANTOSO
E-Journal Menara Perkebunan Vol 76, No 2: Desember 2008
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Summary Attempts to increase cocoa production in Indonesia have been hinderred by attack of CPB (Conopomorpha cramerella). There has been no effective measures to control this pest leading to development of cacao planting materials which resistant to the pod borer. One of genes functioning in plant defense system against insect pests such as catepilar is Proteinase Inhibitor (PIN). This research aimed to isolate and characterize TcPIN gene of cacao pod wall. A clone of TcPIN was isolated with RT-PCR technique using total RNA of cacao pod wall and DNA primer designed based on the sequence Trypsin Inhibitor of cocoa bean accessible online. BlastX analysis of the sequence of the cDNA clone demonstrated that the ± 600 bp gene cloned with pGEM-T was PIN gene as indicated by highly homologous to Trypsin Inhibitor of Theobroma microcarpum resulted in 248 Score bits and E value 1 e-64. Two sequence alligment with the putative 21 kDa PIN of cacao seed indicated a moderately high homology. Contrasting these two sequences however found some non identical amino acids implying some variations. Ringkasan Usaha peningkatan produksi kakao di Indonesia terkendala antara lain oleh adanya serangan hama PBK (Conopomorpha cramerella). Untuk menanggulangi serangan PBK tersebut perlu adanya satu cara pengendalian yang efektif dan efisien, sehingga dapat mendorong usaha pengembangan bahan tanam yang tahan PBK. Salah satu gen membawa sifat ketahanan tanaman terhadap hama ulat adalah Proteinase Inhibitor (PIN). Penelitian ini bertujuan untuk mengisolasi dan mengkarakterisasi gen TcPIN dari kulit buah kakao. Klon cDNA TcPIN diisolasi dari kulit buah kakao dengan teknik RT-PCR meng-gunakan RNA total kulit buah kakao dan primer DNA yang dirancang atas dasar sekuen Inhibitor Tripsin biji kakao yang diakses lewat internet. Hasil analisis BlastX dari sekuen klon cDNA menunjukkan bahwa gen berukuran ± 600 pb yang telah diklon dengan pGEM-T tersebut adalah PIN karena memiliki homologi yang tinggi terhadap 21 kDa trypsin inhibitor dari Theobroma microcarpum yang meng-hasilkan Skor 248 bits dengan Nilai E 1e-64. Penjajaran dua sekuen dengan PIN putatif 21 kDa yang berasal dari biji kakao menunjuk-kan tingkat homologi yang tinggi, dengan perbedaan nyata sehingga dapat terlihat bahwa keduanya tidak identik.

Identifikasi dan isolasi promoter gen pembungaan kakao TcLFY Identification and isolation for promoter of TcLFY cacao flowering gene Djoko SANTOSO; Agustina A. HANDAYAN; Sukarti MOELJOPAWIRO
E-Journal Menara Perkebunan Vol 75, No 1: Juni 2007
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

SummaryPromoter is a regulator of geneexpression for a phenotype or trait carried bythe gene. In the structure, a promoter locatedbeyond the 5’ end of the open reading frame ofthe gene on which its expression is regulated.This research aimed to isolate the DNAfragment flanking TcLFY at the 5’ end and toanalyze whether the fragment has charac-teristics of the promoter, primarily the coremotifs of promoter. Using Genome Walkingtechnique, DNA fragments flanking the TcLFYgene at its 5’ end was isolated. Analysis of theDNA sequence was done using onlinecomputer software accessible through web sitewww.softberry.com and an entry sequence ofthe flanking DNA fragment along with the 2.5kb TcLFY sequence. The result indicated thatthe flanking fragment has core motifs for apromoter at proper positions, which are TATAbox at position –80, CAT boxes (CCAAT) at -387 and –626, and GC boxes that are known asUAS were found at the -323 and –537positions. To obtain a conclusive result, thispromoter sequence needs to be furtherexamined to confirm its function.RingkasanPromoter merupakan pengendali ekspresigen untuk memunculkan fenotipe atau karakteryang dibawa oleh gen tersebut. Di dalamstrukturnya, promoter umumnya terletak didaerah ujung 5’ gen yang dikendalikanekspresinya. Tujuan penelitian ini adalahmendapatkan fragmen DNA yang mengapitgen pengendali pembungaan kakao (TcLFY)dan menganalisisnya apakah memilikikarakteristik promoter, yaitu mengandungmotif-motif inti (core motifs) dari promoter.Dengan teknik Genome Walking, fragmenDNA pengapit gen TcLFY di ujung 5’ dapatdiisolasi. Analisis sekuen menggunakanperangkat lunak komputer online (www.softberry.com) dengan input data fragmentersebut ditambah gen TcLFY 2,5 kb dibawahnya, mengindikasikan adanya beberapamotif inti promoter pada posisi yang sesuai,yaitu kotak TATA pada lokasi –80, kotak CAT(CCAAT) di posisi -387 dan –626, dan kotakGC yang merupakan UAS dijumpai padalokasi -323 dan –537. Untuk memperoleh hasilyang bersifat konklusif, sekuen promoter inimasih perlu diuji fungsinya.

Ekspresi fenotipe gen APETALA1 kakao (TcAP1) pada eksplan tembakau Phenotypic expression of cacao APETALA1 (TcAP1) in tobacco explant Tetty CHAIDAMSARI; . SAMANHUDI; Asmini BUDIANI; Roedhy POERWANTO; Djoko SANTOSO
E-Journal Menara Perkebunan Vol 74, No 1: Juni 2006
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Summary APETALA1 (AP1) is one of flowering identity genes that determines the formation of sepal and petal tissues. An AP1 homologue was cloned from cacao flowers by bio-techniques coupled with bio-informatics. Examination of phenotypic expression was conducted with transgenesis of the 35S-TcAP1 construct using leaf disk technique of tobacco leaf explants mediated by Agrobacterium tumefaciens. PCR specific to TcAP1 demonstrated that the technique is effective in introducing the 35S-TcAP1 construct into tobacco plant cells. RT-PCR with total RNA from the leaves of transgenic tobacco plantlets showed that expression levels of the TcAP1 events varied. The variation of the transcript levels was comparable to the morphological phenotype of the tobacco plantlets grown in vitro. The cultures expressing TcAP1 at moderate levels, have developed into intact plantlets and set up flowers in vitro.Ringkasan APETALA1 (AP1) diketahui merupakan salah satu gen identitas pembungaan yang mengendalikan terbentuknya jaringan sepal dan petal. Homolog AP1 telah diklon dari organ bunga kakao (TcAP1) dengan kombinasi bio-techniques dan bio-informatics. Pengujian ekspresi fenotipe TcAP1 dilakukan dengan transgenesis konstruk konstitutif 35S-TcAP1 menggunakan teknik leaf disk eksplan daun tembakau dan mediasi Agrobacterium tumefaciens. Pengujian PCR spesifik TcAP1 menunjukkan bahwa teknik tersebut cukup efektif dalam mengintroduksikan konstruk 35S-TcAP1 ke dalam sel tanaman tembakau. RT-PCR dari daun planlet tembakau trangenik membuktikan bahwa tingkat ekspresi TcAP1 tersebut bervariasi. Perbedaan level ekspresi TcAP1 ini memberikan pengaruh yang nampak sebanding terhadap perkembangan morfologis planlet tembakau in vitro. Kultur yang mengekspresikan TcAP1 pada level sedang mampu beregenerasi menjadi planlet sempurna dan membentuk bunga in vitro.

Respons awal pemberian biostimulan Orgamin pada kelapa sawit (Elaeis guineensis Jacq.) di Kebun Marjandi PTPN IV Early response of Orgamin biostimulan application in oil palm (Elaeis guineensis Jacq.) at PTPN IV Marjandi plantation Soekarno Mismana PUTRA; Djoko SANTOSO; Happy WIDIASTUTI; A. H. SARAGIH SARAGIH; M. A. GHONI GHONI; B. MARAHIMIN MARAHIMIN; K. PANJAITAN PANJAITAN
E-Journal Menara Perkebunan Vol 81, No 1: Juni 2013
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

AbstractEffort to increase the production of oil palm can beconducted through application of plant growth regulator(PGR). Orgamin biostimulan is a natural PGR formulathat has been tested to improve the vegetative growths ofcorn and oil palm in the glass house. Assessment ofOrgamin and Orgamin plus (Orgamin + micro nutrient)applications at commercial scale was carried out inMarjandi oil palm plantation of PTPN IV usingrandomized block design with three treatments, i.e. K =100% recommended dose of inorganic fertilizer(control), O= Orgamin (1.5 kg/tree) + 50% dose ofinorganic fertilizer, OP = Orgamin plus (1.5 kg/tree)without inorganic fertilizer. The parameters ofobservation at 2.5 months after the treatments were soiland leaf nutrient contents (N, P, K, Mg), percentage offemale flower, mesocarp oil content, and harvested freshfruit bunches (FFB). The observation showed that therewas an increased in oil yield, weight of FFB and leafnutrient content, while the percentage of female flowerand nutrient content of soil were not significantlydifferent compared to the control.AbstrakUpaya untuk meningkatkan produksi kelapa sawitdapat dilakukan antara lain melalui pemberian zatpengatur tumbuh (ZPT). Biostimulan Orgamin merupa-kan formula ZPT alami yang telah diuji di rumah kacapada tanaman jagung dan bibit kelapa sawit. Uji cobaaplikasi Orgamin dan Orgamin plus (Orgamin yangdiperkaya hara mikro) pada skala lapang dilakukan dikebun kelapa sawit Marjandi PTPN IV denganmenggunakan Rancangan Acak Kelompok (RAK) untukmenguji tiga perlakuan, yaitu 1) K (kontrol) = 100%dosis anjuran pupuk kimia (APK = kontrol), 2) O = 50%dosis APK + Orgamin (1,5 kg/pohon), 3) OP = Orgaminplus (1,5 kg/pohon) tanpa pupuk kimia. Peubah yangdiamati pada 2,5 bulan setelah perlakuan adalah kan-dungan hara tanah dan daun (N, P, K, Mg), persentasebunga betina, rendemen minyak mesokarp, dan produksitandan buah segar (TBS). Hasil yang diperoleh menunjukkan terdapat peningkatan rendemen minyak, bobotTBS dan kandungan hara daun, sedangkan persentasebunga betina dan kandungan hara tanah tidak menunjuk-kan perbedaan yang nyata antara perlakuan dan kontrol.

Application of organic fungicide in controlling basal stem rot disease for mature oil palm Happy WIDIASTUTI; Hayati MINARSIH; Djoko SANTOSO; Deden Dewantara ERIS; Galuh Wening PERMATASARI
E-Journal Menara Perkebunan Vol 88, No 1 (2020): April, 2020
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Ganoderma is a major pathogen in oil palm crops. Some efforts related to control the growth of Ganoderma have been conducted but still have not found an effective method. This study aims to develop an organic fungicide that has been tested in vitro, which effective in controlling the growth of Ganoderma. The optimization carried out includes the determination of the dose and time interval for application in 13-year-old mature oil palm. This organic fungicide application was the continuation of application during the previous year especially for the two best treatment which is application organic fungicide every week (1w) and every two weeks (2w). In this study, the treatments tested were three levels dose of organic fungicide (0, 1x and 2x) and two types of frequency application, i.e. every week (1w) and every other week (2w). The results showed that the best application of organic fungicides was every week application with twice doses (1w.2x), based on the parameters of the inhibition of Ganoderma’s fruiting body formation, primary and secondary root formation, the opening of spear leaves, and harvesting parameters. The application of organic fungicide able to recover the oil palm infected Ganoderma sp., with increasing the fresh fruit bunch and its weight around 70% and 78%, respectively.

Keefektifan Agrobacterium mentransfer gen P5CS ke dalam kalus tebu klon PS 851 Effectiveness of Agrobacterium to transfer P5CS gene into sugarcane callus PS 851 clone Niyyah FITRANTY; F NURILMALA; Djoko SANTOSO; Hayati MINARSIH
E-Journal Menara Perkebunan Vol 71, No 1: Juni 2003
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Summary Transformation of a P5CS gene construct into plant cells coupled with regeneration for transgenic plantlets should develop sugarcane tolerant to drought stress. The purpose of the research is to increase the effectiveness and efficiency of Agrobacterium transferring the gene into sugarcane callus. In this method, recombinant plasmid of pBI-P5CS could be transferred into host cells of Agrobacterium LBA4404 through triparental mating with pRK2013 helper. The parameters were tested to increase the effectiveness and efficiency of Agrobacterium transferring the gene into sugarcane callus were the addition of antioxidant and 1.0% glucose, callus age (2, 3, and 4 weeks), medium pH (4.5; 5.0; and 5.6), treated with air dry for 30 minutes, wetting agent of silwet with and without short vacuum treatment, and acetosyringone consentration (100, 500, and 1000 mg/L). Identification of the transgene in sugarcane was conducted by PCR using spesific primers, and the expression was tested by measuring of the proline content. The result showed that addition of acetosyringone 100 ppm or more, P5CS transfer into the sugarcane explants by Agrobacterium was effective. The genetic transformation could be optimized by selecting proper age of calli, which was four weeks after sub-culture. The effectiveness could be maintained and slightly improved by inoculation at pH 4.5, addition 1.0% glucose, wetting agent of silwet with short vacuum treatment, or treated with air drying for 30 minutes. In vitro cultures for transgenic regeneration required addition of antioxidant to prevent browning in the culture media. The amplified DNA fragment demonstrated that the gene was transferred into sugarcane plantlets, and P5CS gene expression showed increasing proline content in transgenic sugarcane plantlets.Ringkasan Transformasi transgen P5CS yang diikuti dengan regenerasi tanaman transgeniknya diper-kirakan mampu menghasilkan tanaman tebu transgenik yang toleran terhadap cekaman kekeringan. Penelitian ini bertujuan untuk me-ningkatkan efektivitas dan efisiensi Agro-bacterium mentransfer gen P5CS ke dalam kalus tebu. Dalam metode ini, plasmid rekombinan pBI-P5CS berhasil dengan baik ditransformasi-kan ke dalam sel. Agrobacterium LBA4404 dengan pendekatan triparental mating meng-gunakan helper pRK2013. Parameter yang diuji untuk meningkatkan kondisi efektif dan efisien dalam transfer gen P5CSke dalam kalus tebu adalah penambahan antioksidan dan glukosa 1,0%, umur kalus (2, 3, dan 4 minggu), pH medium (4,5; 5,0; dan 5,6), pengeringan kalus 30 menit, bahan pembasah silwet tanpa dan dengan pemakuman, dan konsentrasi aseto-siringon (100, 500, dan 1000 mg/L). Pengujian keberadaan transgen P5CS dilakukan dengan PCR menggunakan primer spesifik, sedangkan ekspresinya diuji dengan mengukur kandungan prolin dari tanaman tebu. Hasil percobaan menunjukkan bahwa dengan penambahan asetosiringon 100 ppm atau lebih, penggunaan Agrobacterium terbukti efektif dan efisien dalam transfer konstruk transgen P5CS ke dalam eksplan kalus tebu. Transformasi dapat dioptimalkan dengan memilih eksplan kalus tebu yang baik, yaitu yang umur subkulturnya empat minggu. Efektivitasnya juga dapat dijaga atau sedikit ditingkatkan dengan inokulasi pH 4,5, penambahan glukosa 1,0%, bahan pembasah silwet dengan pemakuman, ataupun pemberian perlakuan pengeringan udara selama 30 menit. Kultur kalus transgenik memerlukan penambahan antioksidan untuk mencegah terjadinya pen-cokelatan. Adanya fragmen DNA hasil amplifikasi dengan primer spesifik P5CS menunjukkan pada tanaman tebu telah terdapat gen P5CS. Demikian pula dengan ekspresi gen P5CS, menunjukkan adanya peningkatan kandungan prolin pada tanaman tebu transgenik.

Co-Authors . Mansyurdin . SAMANHUDI . SYAFARUDDIN A. H. SARAGIH SARAGIH A.R. PURBA PURBA Abdul Mollah S. JAYA Agus Laesanpura Agustina A. HANDAYAN Aida Farida Ajeng Nuzulia H Antonius Suwanto Anwar, Aswaldi Aprih Santoso Asmini Budiani Auzar SYARIEF B. MARAHIMIN MARAHIMIN Bambang S PURWOKO Bambang Wahyudiyono Basil J NIKOLAU Budi Sulistijo Candra Auromiqo Christantius Dwiatmadja Deden Dewantara ERIS DEDI SOLEH EFFENDI Dini Astika SARI Efendi, Darda F NURILMALA Fauziatul FITRIYAH GALUH WENING PERMATASARI Hajrial ASWIDINNOO HAJRIAL ASWIDINNOOR Hanny Hafiar Happy Widiastuti HAPPY WIDIASTUTI Hayati MINARSIH Hayati Minarsih I GEDE PUTU WIGENA Imron Riyadi Indarto Indarto Indarto Irma KRESNAWATY Isnu Irwantoro Jayawarsa, A.A. Ketut Jisman SINAGA K. PANJAITAN PANJAITAN M. A. GHONI GHONI Mayta Novaliza Isda Memed WIRAMIHARDJA Muhammad Jusuf Muhammad Munir Musliar Kasim Niyyah FITRANTI Niyyah FITRANTY Oktaviany Ferry TRIASTANTO Patni Ninghardjanti Pratama, Azka Dhiya R.D.B LEFROY Rita Hayati Riza A PUTRANTO Riza A. PUTRANTO Roedhy Poerwanto Roesalia Anggraenie SATRIYAS ILYAS Soekarno Mismana Putra Suharyanto Sukarti Moeljopawiro Tetty CHAIDAMSARI Tri Panji Umi Rochayati VS Ariyanto Wyati Saddewisasi Yatini Y Yora FARAMITHA Yuli Budiati Yuniarti Anis Pramukawati

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