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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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Biokonversi CPO dengan desaturase amobil sistem kontinu pada skala semipilot untuk produksi minyak mengandung GLA Bioconversion of CPO using immobilized desaturase in continuous system at semipilot scale to produce oil containing GLA . SUHARYANTO; . TRI-PANJI; M Irfani ABDULLAH; Khaswar SYAMSU
E-Journal Menara Perkebunan Vol 74, No 2: Desember 2006
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (170.541 KB) | DOI: 10.22302/iribb.jur.mp.v74i2.111

Abstract

Summary Gamma linolenic acid (GLA) is a polyunsaturated fatty acid having high economic value as healthy oil. Research at laboratory scale showed that Absidia corymbifera and Rhizopus sp. fungi have the ability to increase unsaturation level of crude palm oil (CPO) and GLA formation through enzymatic bioconversion.  Stability of desatu-rase enzyme, especially ∆6 and ∆12 having significant role in this process could be enhanced by applying immobilization technique. The current research objective was to determine optimum process of CPO bio-conversion using immobilized desaturase enzyme using continuous system at semipilot scale to produce CPO containing GLA.  Crude  desaturase enzyme of A. corymbifera biomass was immobilized with zeolite particles and used for optimization of CPO bioconversion in continuous system at semipilot scale (15,000 mL per day). Optimization of bio-conversion conditions included flow rate of substrate, size of zeolite for immobilization, and enzyme stability during process.  The result showed that desaturase immobilized in small size particles of zeolite (1-3 mm) gave higher increase unsaturation level with average desaturase activity of 7.84 U, compared to that immobilized in larger zeolite  particles (8-10 mm), which reached average desaturase activity of 4.67 U.  However, the use of small zeolite particles often caused plugging substrate flow. The activity of immobilized desaturase in continuous  system was stable for 9-18 hours. Optimum flow rate of substrate using small zeolite particles (1-3 mm) was  850 mL/min, while that of using larger zeolite particles (8-10 mm) was 875 mL/min.  The bioconversion of CPO at optimum condition yielding 1.58% (w/w) GLA from initial concentration of linolenic acid 0.29%. RingkasanAsam γ-linolenat (GLA) merupakan asam lemak takjenuh majemuk yang memiliki nilai ekonomi tinggi sebagai minyak kesehatan. Penelitian pada skala laboratorium me-nunjukkan bahwa Absidia corymbifera dan Rhizopus sp. memiliki kemampuan untuk me-ningkatkan ketidak-jenuhan minyak sawit mentah (CPO) dan menghasilkan GLA melalui biokonversi enzimatis. Stabilitas enzim desaturase, khususnya ∆6 dan ∆12yang berperan pada proses ini dapat ditingkatkan antara lain melalui teknik amobilisasi. Penelitian lanjutan ini bertujuan menetapkan kondisi optimum biokonversi CPO untuk menghasilkan minyak yang kaya akan asam lemak takjenuh majemuk, khususnya GLA menggunakan enzim desaturase amobil sistem kontinu pada skala semipilot.  Ekstrak kasar enzim desaturase asal biomassa fungi             A. corymbifera diamobilisasi dengan butiran zeolit dan selanjutnya digunakan untuk optimasi proses biokonversi secara kontinu pada skala semipilot (15.000 mL per hari). Optimasi proses kontinu meliputi laju alir substrat, ukuran butiran zeolit, dan stabilitas enzim selama proses. Hasil penelitian menun-jukkan bahwa desaturase yang diamobilisasi pada zeolit berukuran kecil (1-3 mm) memberikan peningkatan ketidakjenuhan yang lebih tinggi dengan aktivitas rata-rata 7,84 U, dibandingkan dengan yang diamobilisasi pada zeolit berukuran besar (8-10 mm) dengan aktivitas rata-rata 4,67 U. Namun, penggunaan zeolit berukuran kecil sering menimbulkan sumbatan aliran substrat. Aktivitas desaturase amobil pada proses kontinu dapat bertahan selama 9-18 jam. Laju alir optimum substrat pada penggunaan zeolit berukuran kecil (1-3 mm) adalah 850 mL/menit, sedangkan pada penggunaan zeolit besar (8-10 mm) adalah 875 mL/menit. Biokonversi CPO pada kondisi optimum menghasilkan GLA 1,58% (b/b) dari kandungan asam linolenat awal 0,29%tration of linolenic acid 0.29%.
The development of somatic embryos of sago palm (Metroxylon sagu Rottb.) on solid media *) Perkembangan embrio somatik tanaman sagu (Metroxylon sagu Rottb.) pada medium padat Imron RIYADI; J.S. TAHARDI TAHARDI; . SUMARYONO
E-Journal Menara Perkebunan Vol 73, No 2: Desember 2005
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (297.957 KB) | DOI: 10.22302/iribb.jur.mp.v73i2.155

Abstract

SummarySago palm (Metroxylon sagu Rottb.) isusually propagated vegetatively by suckers.However, the limited availability of uniformsuckers is a major obstacle in the establishmentof cultivated sago plantations. Tissue culture hasthe potential for large-scale mass clonalpropagation of superior genotypes of sago palm.In vitro culture of sago palm has been establishedthrough somatic embryogenesis. Embryogeniccallus derived from shoot apical tissue of youngsuckers was cultured on a modified Murashigeand Skoog (MMS) medium containing 30 g/Lsucrose, 2 g/L Gelrite, 1 g/L activated charcoal,5.0 mg/L 2,4-D, and 0.1 mg/L kinetin to inducesomatic embryos. Callus clumps formed somaticembryos within four weeks. In the subsequentculture, approximately 0.3 g initial globularcallus grown on MMS medium containing 1.0mg/L kinetin, 0.01 mg/L ABA and 0.1 mg/L GA 3produced 140 to 200 somatic embryos at differentdevelopmental stages four weeks later. All stagesof developing embryos with different sizesand colors were present at any one time ofculture. Secondary (repetitive) somatic embryo-genesis was also found in the culture.Transferring of the mature stage of somaticembryos to solid media with half-strength macro salts and with sucrose at concentration of 20 or 30 g/L without growth regulators led to the development of normal plantlets.RingkasanTanaman sagu (Metroxylon sagu Rottb.)biasanya diperbanyak secara vegetatif dengantunas anakan. Namun, terbatasnya ketersediaantunas anakan yang seragam merupakanhambatan utama dalam pembukaan perkebunansagu. Teknologi kultur jaringan mempunyaipotensi untuk perbanyakan klonal tanaman saguunggul dalam skala besar. Kultur in vitrotanaman sagu telah dikembangkan melaluiembriogenesis somatik. Kalus embriogenik yangberasal dari eksplan pucuk tunas anakandikulturkan pada medium modifikasi Murashigedan Skoog (MMS) dengan sukrosa 30 g/L,Gelrite 2 g/L, arang aktif 1 g/L, 2,4-D 5 mg/Ldan kinetin 0,1 mg/L untuk menginduksi embriosomatik. Kalus membentuk embrio somatikdalam waktu empat minggu. Dalam kulturberikutnya, dari kurang-lebih 0,3 g embrio faseglobuler yang dikulturkan pada medium MMSdengan kinetin 1,0 mg/L, ABA 0,01 mg/L danGA 3 0,1 mg/L menghasilkan 140 sampai 200embrio somatik dengan fase perkembangan yangberbeda-beda. Embrio somatik dalam semuafase perkembangan dengan ukuran dan warnayang berbeda-beda ditemukan setiap saat dalamkultur. Di samping itu, embriogenesis somatiksekunder (berulang) juga terjadi dalam kultursagu. Embrio somatik fase dewasa biladipindah ke medium padat dengan garam makrosetengah konsentrasi dan sukrosa padakonsentrasi 20 atau 30 g/L tanpa zat pengaturtumbuh akan menjadi planlet normal.
Isolasi dan mikroenkapsulasi vitamin E dari crude palm oil sebagai sumber antioksidan bahan pangan Isolation and microencapsulation of vitamin E from crude palm oil as source of food antioxidant Irma KRESNAWATY; Asmini BUDIANI; . TRI-PANJI; . SUHARYANTO
E-Journal Menara Perkebunan Vol 80, No 2: Desember 2012
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (268.43 KB) | DOI: 10.22302/iribb.jur.mp.v80i2.38

Abstract

AbstractIn order to increase  value added  and  to support downstream industry of  palm oil, minor components of the oil such as β-carotene and vitamin E should be utilized. Vitamin E is a high value  vitamin  that could be used as material for pharmaceutical and  neutraceutical products. Technological constraints encountered in the utilization of  vitamin E from CPO are lack of optimal extraction and purification method as well as the way to stabilize of the product. The research was conducted to find optimal extraction and purification method of vitamin E from CPO and microencapsulation method of vitamin E as pharmaceutical and neutraceutical product. The research showed that vitamin E could be recovered  from CPO by several steps process including saponification using NaOH, separation of unsaponificated  solution,  followed by dissolution using 2-propanol in hexane and extraction  using methanol. Raw extract of vitamin E was then purified by coloumn chromatography with stationary phase of silica gel and mobile phase (eluent) of petroleum benzene/ diethyl ether/acetic acid 70 : 30 : 0,2. Purified vitamin E could be collected as fraction 4-8. Vitamin E obtained  had  similar antioxidant activity as in pure vitamin E (Sigma) and vitamin C. Microencapsulation method could be conducted using arabic gum as coating material followed by spray drying and resulted IC50-DPPH value 132.55  ppm which considered middle activity category.AbstrakUntuk meningkatkan nilai tambah dan mengem-bangkan industri hilir minyak kelapa sawit (CPO), komponen minor minyak tersebut seperti vitamin E dan β-karoten perlu dimanfaatkan. Vitamin E merupakan produk bernilai ekonomis tinggi sebagai bahan farmaseutikal dan neutrasetikal. Kendala yang dihadapi dalam pemanfaatan vitamin E dari CPO, yaitu belum tersedianya teknik ekstraksi dan purifikasi yang optimal dan cara memper-tahankan stabilitas vitamin E. Penelitian ini bertujuan untuk memperoleh teknik ekstraksi dan purifikasi vitamin E dari CPO dan teknik mikroenkapsulasi vitamin E sebagai bahan farmaseutikal dan neutrasetikal.  Hasil penelitian menunjukkan bahwa vitamin E dapat diproduksi dengan beberapa tahapan yakni saponifikasi dengan NaOH, pemisahan lapisan pekat tak tersabunkan, pelarutan dengan2-propanol dalam heksana, ekstraksi dengan metanol dan pelarutan ekstrak dengan 2-propanol dalam heksana. Ekstrak kasar vitamin E dimurnikan dengan kromatografi kolom dengan fasa diam silika gel dan fasa gerak petroleum benzen/dietil eter/asam asetat = 70 : 30 : 0,2. Vitamin E dapat dimurnikan pada fraksi ke-4 sampai dengan ke-8. Aktivitas antioksidan vitamin E hasil ekstraksi tersebut setara dengan vitamin E murni (Sigma). Teknik mikroenkapsulasi vitamin E hasil ekstraksi dari CPO dapat dilakukan dengan penyalut gum arab dan pengeringan dengan spray dryer  yang menghasilkan anti-oksidan dengan aktivitas IC50 DPPH = 132,55 ppm yang termasuk kategori beraktivitas sedang.
Respons biokimia beberapa progeni kelapa sawit (Elaeis guineensis Jacq.) terhadap cekaman kekeringan pada kondisi lapang Biochemical responses of several oil palm (Elaeis guineensis Jacq.) progenies to drought stress in field condition Nurita TORUAN-MATHIUS; . TONY-LIWANG; M IBRAHIM-DANUWIKARSA; G. SURYATMANA; H DJAJASUKANTA; D SAODAH; I GP WENTEN ASTIKA
E-Journal Menara Perkebunan Vol 72, No 2: Desember 2004
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (276.157 KB) | DOI: 10.22302/iribb.jur.mp.v72i2.121

Abstract

Summary        Oil palm have swallow roots, it caused the plant untolerant to drought  stress  and will decrease 10-40% bunch fresh weight in drought condition. Response of oil palm to drought stress in field conditions still unknown. The objective of these research  is to obtain  biochemical character  which has significant correlation with drought  tolerance, and to obtain tolerant progeny with high yield (fresh bunch weight) in drought condition.  The experiment were conducted in Riau (Kandista estate) and South Kalimantan  (Batu Mulia estate), with different of soil type and rainfalls. Observation were done in four times in different  month with different rainfalls. On each time of observation were analyzed  proline, glycine betaine, ornithine-δ-aminotransferase (δ-OAT) enzyme content, as biochemical variables and bunch weigth as yield variable response.  Eleven oil palm progenies 10-year-old grown in field divided with three block (as replication), each plot consisted of 16 plants. Data  were analyzed with Combined Experiment Analysis, Principal Component Analysis, Multiple Regression Analysis,  and Path Analysis. The results showed that eleven progenies gave different responses to drought stress in each variable, location and  time of observation. Most of progenies reponsive to two or three biochemical characters. Progeny 52 has no correlation with most of biochemical characters. Progeny 33 responsive with proline, while  progeny 85, 91 and  93 have high responsive to protein.  Proline, δ-OAT enzyme, and protein have high correlation with bunch weight.  Proline, and δ-OAT enzyme, categorized as biochemical characters of oil palm tolerance to drought stress. Progeny 33 more tolerance to drought stress compare with others progenies, and have highest productivity in Batu  Mulia estate. Ringkasan         Tanaman kelapa sawit memiliki perakaran yang dangkal sehingga mudah mengalami cekaman   kekeringan   yang dapat    menurunkan hasil TBS 10 - 40%. Respons tanaman kelapa  sawit terhadap cekaman kekeringan dalam kondisi lapang masih sangat sedikit sekali diketahui. Tujuan penelitian ini adalah untuk mendapatkan penciri biokimia yang berperan dalam sifat toleran tanaman terhadap cekaman kekeringan dan hubungan penciri biokimia dengan hasil tandan buah segar (TBS), serta menetapkan progeni yang toleran dan  ber-produksi tinggi pada lokasi yang tercekam. Percobaan dilakukan di dua lokasi perkebunan yang terletak di Riau (perkebunan Kandista) dan Kalimantan Selatan (perkebunan Batu Mulia) yang berbeda tipe tanah dan  curah hujannya. Pengamatan dilakukan pada empat waktu, pada bulan yang berbeda curah hujannya. Pada keempat waktu tersebut dianalisis kadar prolin, glisin-betain, enzim ornitin-δ-aminotransferase (δ-OAT), dan protein sebagai variabel respons biokimia serta hasil TBS sebagai variabel respons produktivitas tanaman kelapa sawit.  Tiap lokasi percobaan menggunakan rancangan kelompok lengkap teracak.  Tanaman kelapa sawit berumur 10 tahun sebanyak 11 progeni yang telah ada di lapangan, ditetapkan sebanyak tiga blok (sebagai ulangan).  Tiap plot percobaan berisi 16 tanaman.  Data yang diperoleh dianalisis dengan analisis statistika percobaan tergabung, analisis kom-ponen utama, regresi berganda dan analisis jalin. Hasil penelitian menunjukkan bahwa ada perbedaan respons 11 progeni kelapa sawit ter-hadap cekaman kekeringan pada masing-masing variabel respons dalam lokasi dan waktu pengamatan yang berbeda. Seluruh progeni responsif terhadap dua atau tiga penciri biokimia selama waktu penelitian berlangsung, kecuali progeni 52 tidak memiliki korelasi dengan seluruh penciri biokimia. Progeni 33 responsif terhadap prolin, sedang  progeni 85, progeni 91 dan progeni 93 cukup responsif terhadap protein. Prolin, enzim δ-OAT, dan protein berhubungan erat dengan hasil TBS. Prolin, enzim δ-OAT, dan protein dapat dikatagorikan sebagai penciri biokimia terhadap cekaman kekeringan  pada tanaman kelapa sawit. Progeni 33 lebih toleran terhadap cekaman kekeringan dibandingkan  dengan progeni lainnya dan produktivitasnya  tertinggi  di   perkebunan  Batu  Mulia.
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
E-Journal Menara Perkebunan Vol 77, No 2: Desember 2009
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (218.119 KB) | 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.
Kloning dan karakterisasi daerah promoter gen penyandi ADP glucose pyrophosphorylase dari Metroxylon sagu rendemen pati-tinggi dan -rendah [Cloning and characterization of promoter region of ADP glucose pyrophosphorylase-encoding gene from Metroxylon sagu with high- and low-starch content] Asmini BUDIANI; Riza Arief PUTRANTO; Hayati MINARSIH; Imron RIYADI; . SUMARYONO; Barahima ABBAS
E-Journal Menara Perkebunan Vol 84, No 1: Oktober 2016
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22302/iribb.jur.mp.v84i1.200

Abstract

ADP-glucose pyrophosphorylase (AGPase) is one of the key enzymes in the starch biosynthesis. In many plants, the activity of this enzyme was reported to affect the yield and composition of the produced starch. This research is a part of an effort to develop molecular markers for early selection of high starch-yielding of sago palm. The purpose of the research was to isolate promoters of AGP gene and to analyze the differences in their DNA sequences between sago palm with high starch content (MsHS) and low starch content (MsLS). DNA was isolated and purified from the leaves of the two sago palm. The promoter region of AGP was amplified by Genome Walking technique. The specific primers were designed by Primer3 program based on the information of DNA sequence of AGP genes of sago palm from previous studies. Selected DNA fragments resulted from Genome Walking were isolated from the gel, cloned into E. coli, and analyzed its DNA sequence. DNA sequence analysis showed that one DNA fragment from MsHS  (± 1500 bp) and one DNA fragment from MsLS (> 2000 bp) were confirmed as a 5’ upstream of the AGP gene.  Further in silico analysis using MEME program identified various DNA motifs of cis-acting elements, which confirmed that those DNA fragment were promoter region of the gene. Preliminary analysis showed the differences in DNA sequences and motives of cis-acting elements in the promoter region of the two samples which might influence or indirectly associated with the character of the starch yield in sago palm.
Karakteristik gugus fungsional eksopolisakarida Burkholderia cenocepacia strain KTG dalam tiga kelas tekstur tanah The characteristic of exopolysaccharide functional group of Burkholderia cenocepacia strain KTG in three soil texture classes Laksmita Prima SANTI
E-Journal Menara Perkebunan Vol 79, No 2: Desember 2011
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (153.67 KB) | DOI: 10.22302/iribb.jur.mp.v79i2.57

Abstract

Abstract This research was carried out to investigate the characteristics of exopolysaccharide functional groups of Burkholderia cenocepacia strain KTG originated from three different soil texture classes. This bacterium was isolated from rhizosphere of oil palm (Elaeis guineensis Jacq.) and has a highly potential exopolysaccharides production (4.3- 5.8 mg/mL) promoting soil aggregate formation. Fouriertransformed infrared spectroscopy (FTIR) was used for obtaining vibrational spectra of the exopolysaccharide. The bacterium was cultured in ATCC no.4 medium with a different source of carbon i.e. 2% (w/v) of sucrose, glucose, manitol, lactose, and 4-hydroxy-phenyl acetic acid as carbon sources respectively for initial characterization and then soil suspension of clay, sandy loam, and loamy sand. Analysis of the FTIR spectrum of the exopolysaccharide B. cenocepacia KTG strain both contain similar source of carbon in liquid ATCC no.14 medium and soil solution after 72 hours incubation showed intensive bands in the range of 3403-3400 cm-1 and 1651-1636 cm-1 corresponding to the stretching band of O-H (hydroxyl) and C=O (carbonyl) of exopolysaccharide. In the region 1135-993 cm-1 , exopolysaccharide of B. cenocepacia KTG strain exhibited the characteristic absorption at 1126 cm-1 corresponding to the existence of α and β configurationsAbstrak Penelitian ini bertujuan untuk mempelajari karakteristik gugus fungsional eksopolisakarida Burkholderia cenocepacia strain KTG di dalam tiga kelas tekstur tanah yang berbeda. Bakteri ini diisolasi dari rizosfer kelapa sawit (Elaeis guineensis Jacq) dan memiliki potensi menghasilkan eksopolisakarida dalam jumlah tinggi (4,3-5,8 mg/mL) untuk membentuk agregat tanah. Fourier-transformed infrared spectroscopy (FTIR) digunakan untuk memperoleh gambaran spektra dari eksopolisakarida. Sebagai tahap awal karakterisasi gugus fungsional, bakteri ditumbuhkan di dalam medium ATCC no.14 dengan 2 % (b/v) sumber karbon berbeda yaitu: sukrosa, glukosa, manitol, laktosa, dan 4- hydroxyphenyl acetic acid dan diuji pula dalam larutan bahan tanah berliat, lempung berpasir, dan pasir berlempung. Hasil analisis dengan spektrum menunjukkan bahwa di dalam medium ATCC no.14 dengan jenis karbon berbeda ataupun di dalam larutan tanah setelah inkubasi 72 jam terlihat penyerapan pita yang intensif pada bilangan gelombang 3403-3400 cm-1 dan 1651-1636 cm-1 yang menandakan gugus hidroksil dan karbonil. Pada wilayah bilangan gelombang 1135-992.9 cm-1 , eksopolisakarida B. cenocepacia strain KTG menunjukkan penyerapan spesifik pada bilangan gelombang 1126 cm-1 yang menandakan konfigurasi ikatan α dan β.
Biostimulasi pertumbuhan vegetatif tanaman tebu (Saccharum officinarum L.) pada fase awal di lahan kering (Biostimulation of vegetative growth of sugarcane (Saccharum officinarum L.) in the initial phase on dry land) Sri WAHYUNI; Hanning Susilo HABIBULLAH; Soekarno Mismana PUTRA; Dian Mutiara AMANAH; . SISWANTO; . PRIYONO; Djoko SANTOSO; Saptowo Jumali PARDAL
E-Journal Menara Perkebunan Vol 86, No 2 (2018): Oktober 2018
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (2314.766 KB) | DOI: 10.22302/iribb.jur.mp.v86i2.284

Abstract

AbstractThe expansion of sugarcane areas as a support to national sugar production has shifted to sub-optimal dry land. In drought stress conditions, early growth of sugarcane usually can inhibite and decrease its productivity. This study aimed to test the efficacy of organic biostimulant in increasing vegetative growth of sugarcane in the dry land. Firstly, seedlings were submerged with biostimulant of Citorin-Rfor overnight. Secondly, the biostimulant application of Citorin-S was carried out by foliar sprayat age1 and4 months old trees. Humicacid 0.5% (v/v) was applied in soil before planting while the application of mycorrhiza was carried out by direct pouring on soil during planting. The results showed that the initial vegetative growth of biostimulant-treated sugarcane stem diameter and length were 23% wider and 27% higher compared to that of control, respectively. In subsequent growth cycle, all observed vegetative parameters showed higher growth value in the biostimulant-treated sugarcanes than that of the control. Plant height, stem diameter and number of tillers of biostimulant-treated sugarcanes had significantly higher values than that of the control. P3 treatment (organic biostimulant plus humic acid and mycorrhiza) was the best treatment. The height and diameter of P3 sugarcane stems were 47% wider and 59% higher, respectively, compared to that of control at 107 DAP.[Keywords: biostimulant, plant height, stem diameter, number of tillers, number of leaves] Abstrak Penambahan areal tanaman tebu untuk mendukung peningkatan produksi gula nasional telah bergeser ke areal sub-optimal lahan kering. Pada kondisi cekaman kekeringan, pertumbuhan awal tebu biasanya terhambat dan dapat menurunkan produktivitas saat panen. Penelitian ini bertujuan menguji efikasi biostimulan organik untukmeningkatkan pertumbuhan vegetatif tanaman tebu pada fase awal di lahan kering. Perlakuan biostimulan Citorin-R diaplikasikan pada benih dengan cara perendaman semalam. Perlakuan kedua, biostimulan Citorin-S disemprotkanpada saat tanaman tebu berumur 1 dan 4 bulan secara foliar spray. Aplikasi asam humat 0,5 % (v/v) di tanah dilakukan sebelum tanam, sedangkan aplikasi mikoriza dilakukan dengan pemberian langsung pada tanah saat penanaman bagal tebu. Hasil penelitian menunjukkan bahwa nilai pertumbuhan vegetatif awal tanaman tebu perlakuan memiliki diameter batang sekitar 23% dan tinggi tanaman 27% lebih tinggi daripada tebu kontrol. Pada pertumbuhan selanjutnya, semua parameter vegetatif yang diamati menunjukkan nilai pertumbuhan yang lebih tinggi pada tanaman tebu perlakuan daripada kontrol. Tinggi tanaman, diameter batang dan jumlah anakan secara statistik berbeda nyata lebih tinggi pada tanaman tebu perlakuan daripada kontrol. Perlakuan P3 (biostimulan organik plus asam humat dan mikoriza) adalah perlakuan terbaik. Tinggi dan diameter batang tanaman tebu P3 masing-masing 47% dan 59% lebih besar daripada batang tanaman kontrol pada 107 hari setelah tanam (HST).  [Kata kunci :biostimulan, tinggi tanaman, diameter batang, jumlah anakan, jumlah daun]
Bioactivation of phosphate rocks by indigenous phosphate-solubilizing fungi Bioaktivasi fosfat alam oleh fungi pelarut fosfat setempat H WIDIASTUTI; Didiek H GOENADI; . TRI-PANJI; L P SANTI; P FATURACHIM; N MARDIANA; I HARIANTO; . ISROI
E-Journal Menara Perkebunan Vol 68, No 1: Juni 2000
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (187.525 KB) | DOI: 10.22302/iribb.jur.mp.v68i1.137

Abstract

Ringkasan Efektivitas fungi pelarut fosfat (FPF) dalam meningkatkan kelarutan fosfor (P) fosfat alam (FA) sangat dipengaruhi oleh kesesuaian isolat fungi dengan mineralogi batuan fosfat. Satu seri percobaan laboratorium telah dilakukan untuk menetapkan potensi supernatan kultur cair (SKC) dari FPF asal tanah dan batuan tambang FA eks­Cileungsi dan Madura untuk meningkatkan kelarutan FA eks-Cileungsi (FAQ dan eks­Madura (FAM) dalam pembuatan superfosfat yang diaktivasi secara biologi (SPab). Kegiatan penelitian meliputi: (1) seleksi pelarutan P-FPF dalam medium Pikovskaya, (2) pengujian kemampuan pelarutan P-FAC, P-FAM, P-Ca3 (PO4)z, dan P AIP04 isolat-isolat terseleksi, dan (3) optimasi pembuatan SPab dengan isolat ter­pilih. Rancangan percobaan yang digunakan adalah rancangan acak lengkap dengan dua ulangan. Dari hasil isolasi diperoleh 50 isolat FPF, 17 isolat di antaranya berpotensi dalam melarutkan fosfat yang ditandai pembentukan zona bening yang intensif di sekitar koloni. Dari ketujuh belas isolat tersebut sepuluh isolat berasal dari Lulut (Cileungsi), dan tujuh isolat lainnya berasal dari Madura (masing-masing dua isolat dari Socah dan Aengnyior serta tiga isolat dari Korbe). Berdasarkan kemampuan melarutkan P dari FAC, FAM, Ca3(PO4)2, dan AIP04 diperoleh masing-masing tiga isolat dari Cileungsi dan Madura. Dari keenam isolat tersebut empat isolat di antaranya tergolong Penicillium sp. dan dua isolat lainnya termasuk Aspergillus sp. Di antara keenam isolat tersebut isolat Korbe 0909 memiliki kemampuan iertinggi dalam melarutkan P dari semua sumber P. Kandungan P-FAC lebih tinggi daripada FAM dan mendekati FA eks Maroko. SKC dapat menggantikan fungsi H2SO4 (98%) dalam melarutkan P-FA. SPab Cileungsi mengan­dung P nyata lebih tinggi daripada FAC yang diaktivasi secara konvensional, namun pada SPab Madura kandungan P larut air nyata lebih rendah, sedangkan P larut asam sitrat 2% dan perklorat sebanding dengan FAM yang diaktivasi secara konvensional. Aktivasi FA oleh SKC dapat menurunkan konsentrasi asam fosfat (H3PO4) dari 52% menjadi 42%. Kelarutah P (asam sitrat 2% dan air) dan kandungan sulfur-SPab Cileungsi dan Madura nyata lebih rendah dibandingkan dengan SP36.Summary The effectiveness of phosphate-solubilizing fungi (PSF) in enhancing phosphorus (P) solubility of phosphate rocks (PR) is assumed to be depen­dent on the suitability of the fungal isolate to the mineralogycal composition of the rocks. A laboratory study was conducted to determine the phosphate solubilizing ability of liquid culture supernatants (LCS) of PSF isolated from various PR deposits and adjacent soils, i.e. at Cileungsi in West Java and the island of Madura in East Java to enhance the reactivity of PR from deposits at Cileungsi (CPR) and Madura (MPR) and their potential use as agents in the production of bio­logically-activated superphosphate (SPab). Three series of laboratory experiments were conducted: (1) screening isolate on the solubilization of P in Pikovskaya medium; (2) assaying the ability of selected isolates on solubilization of P-CPR, P­MPR, P-Ca3(P04)2 and P-AIPO4, and (3) optimiz­ing superphosphate fertilizer formulation. Com­pletely random design was used as the exper­imental design with two replicates. Seventeen out of 50 PSF isolates were characterized to be highly potential as phosphate solubilizers, as indicated by clear zone formation. Ten isolates were from Lulut (Cileungsi) and seven from Madura island, two from Socah and Aengnyior respectively, and remaining three from Korbe. Regarding the ability of P solubilization of four P sources, six isolates were selected, three each from Cileungsi and Madura. Of these six isolates, four are Penicillium sp., and four belong to Aspergillus sp. The Asper­gillus sp. isolate Korbe 0909 was found to be the highest in P-solubilization of various sources of P. Based on the P dissolving ability of P-CPR and their effectiveness in substituting for sulphuric acid (98%) usually used in conventional produc­tion of superphosphate, the LCS of Korbe 0909 improved significantly the P-PRs dissolution. MPR activated by the LCS yielded a comparable values of 2% citric acid-soluble P content and significantly lower water-soluble P compared with conventional method: Reduction of phosphoric acid (H3PO4) concentration from 52% to 42%, in combination with LCS treatment, produced P dissolution comparable to the conventional meth­od. Although the P solubilization of CSPab and MsPab in both 2% citric acid and water as well as thus content were significantly lower compared with SP36.
Kemampuan jamur pelapuk kayu isolat JPA dan Trichoderma Sp. S2-2 dalam mendegradasi tandan kosong kelapa sawit untuk menghasilkan selulosa The capability of wood rot fungus JPA isolate and Trichoderma sp. S2-2 in degradation of oil palm empty fruit bunches to produce cellulose . ALHIDAYATULLAH; Lisdar I SUDIRMAN1; Okky Setyawati DHARMAPUTRA
E-Journal Menara Perkebunan Vol 82, No 2: Desember 2014
Publisher : INDONESIAN RESEARCH INSTITUTE FOR BIOTECHNOLOGY AND BIOINDUSTRY

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (238.298 KB) | DOI: 10.22302/iribb.jur.mp.v82i2.17

Abstract

Abstract  Oil palm empty fruit bunches (OPEFB) are the ligno-cellulosic wastes from palm oil processing. They can be used to produce raw materials for value-added products. The purpose of this study was to determine the degradation capacity of JPA wood rot fungi and Trichoderma sp. S2-2 on OPEFB. The 500 g of substrates consisted of 81% of OPEFB, 15% bran, 1.5% lime and 1.5% gypsum were used for growing. The substrates were inoculated with five treatments i.e without isolate (K); with JPA isolate (JPA); with Trichoderma sp. S2-2 (T); with the two isolates (JPA + T); and with JPA isolate and after four weeks of incubation inoculated with Trichoderma sp. S2-2 [(JPA)+T]. All treatments were incubated for eight weeks. The results showed that JPA+T was the best treatment which the two isolates must be inoculated simultaneously for degradation of OPEFB. Lignin and cellulose content on JPA+T treatment respectively were 20.83% and 33.77%. C/N ratio of OPEFB degraded with JPA+T was lower than the C/N ratio of TKKS degraded with Trichoderma harzianum and TKKS degraded with EM4 in previous study. AbstrakTandan kosong kelapa sawit (TKKS) merupakan limbah lignoselulosa dari pengolahan minyak kelapa sawit. TKKS dapat dimanfaatkan untuk memperoleh bahan baku untuk produk bernilai tambah. Tujuan penelitian ini adalah untuk mengetahui kemampuan degradasi jamur pelapuk kayu isolat JPA dan Trichoderma sp. S2-2 pada TKKS. Sebanyak 500 g substrat terdiri dari 81% TKKS, 15% dedak, 1,5% kapur, dan 1,5% gypsum digunakan untuk per-tumbuhan. Substrat diinokulasi dengan lima perlakuan yaitu tanpa isolat (K); dengan isolat JPA (JPA); dengan Trichoderma sp. S2-2 (T); dengan isolat JPA dan setelah empat minggu inkubasi, diinokulasi dengan Trichoderma sp. S2-2 [(JPA+T)]. Semua perlakuan diinkubasi selama delapan minggu. Hasil percobaan menunjukkan bahwa perlakuan JPA+T adalah perlakuan terbaik yaitu kedua isolat tesebut harus diinokulasi secara bersamaan untuk mendegradasi TKKS. Kandungan lignin dan selulosa TKKS dengan  perlakuan  JPA+T   masing-masing  adalah  20,83% dan 33,77%. Rasio C/N TKKS hasil degradasi dengan JPA+T lebih  rendah  daripada  rasio C/N pada TKKS yang didegradasi dengan Trichoderma harzianum dan TKKS yang didegradasi dengan EM4 pada penelitian sebelumnya.

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