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"The whole cell immobilization in ethanol fermentation can be done by using natural carriers or through synthetic carriers. All of these methods have the same purpose of retaining high cell concentrations within a certain defined region of space which leads to higher ethanol productivity. Lignocellulosic plant substance represents one of highlypotential sources in ethanol production. Some studies have found that cellulosic substances substances can also be used as a natural carrier in cell immobilization by re-circulating pre-culture medium into a reactor. In this experiment, rice hulls without any treatment were used to immobilize Saccharomyces cerevisiae through semi solid state incubation combined with re-circulating pre-culture medium. The scanning electron microscopy (SEM) pictures of the carrier showthat the yeast cells are absorbed and embedded to the ricehull pore. In liquid batch fermentation system with an initialsugar concentration of 50 g/L, nearly 100% total sugar was consumed after 48 hours. This resulted in an ethanol yield of 0.32 g ethanol/g glucose, which is 62.7% of the theoretical value. Ethanol productivity of 0.59 g/(L.h) is 2.3 fold higher than that of free cells which is 0.26 g/(L.h). An effort to reuse the immobilized cells in liquid fermentationsystem showed poor results due to cell desorption in the first batch which led to high sugar concentration inhibitory effect in the second batch fermentation. This might be solved by using semi solid fermentation process in the future work. "

"[Telah dilakukan penelitian yang bertujuan untuk mengetahui pengaruh penambahan starter mikroba (Acetobacter aceti, Lactobacillus plantarum dan Saccharomyces cerevisiae) serta pemerasan pulp terhadap fermentasi dan mutu biji kakao. Penelitian menggunakan metode Rancangan Acak Lengkap (RAL) pola faktorial 3x5 dengan dua kali ulangan. Hasil penelitian menunjukkan bahwa penambahan starter meningkatkan konsentrasi etanol pada saat fermentasi dan meningkatkan kadar asam asetat dan asam sitrat, tetapi menurunkan konsentrasi asam oksalat pada biji kakao. Penambahan starter disertai pemerasan pulp menghasilkan biji kakao dengan kadar asam asetat sebesar 0,47%, sedangkan biji kakao tanpa pemerasan menghasilkan kadar asam asetat 0,49%. Penambahan starter disertai pemerasan pulp menghasilkan mutu biji kakao terbaik dengan karakteristik sebagai berikut: skor nilai uji belah tertinggi (379 dari 400), mutu fisik (Golongan mutu A) serta memenuhi persyaratan mutu SNI 2008 No. 2323 tentang biji kakao dengan rasio jumlah per berat biji sebanyak 88 biji/100g; nilai pH 4,93; kadar asam asetat 0,47%, kadar lemak 34,90%, kadar air 4,47%, kadar serat kasar 3,66% dan kadar abu 4,82% dengan waktu fermentasi selama 5 hari.;The aimed of this study was to investigate the effect of starter culture addition (Acetobacter aceti, Lactobacillus plantarum, and Saccharomyces cerevisiae) with depulping on the fermentation and quality of cocoa beans. The experimental design of this study was conducted using a 3×5 factorial Completely Randomized Design (CRD) with duplicate replication. The result revealed that starter addition increased ethanol concentration on the fermentation process, increased acetate acid, and citric acid concentration meanwhile oxalic acid was decreased on cocoa beans during 5 days of fermentation. Depulping caused a slight decrease in acetic acid concentration at the end of fermentation with values of 0,47%, meanwhile the sample of cocoa beans without depulping treatment had acetic acid concentration of 0,49%. Starter culture addition and depulping treatment resulted the best characteristic of cocoa beans which visualized by the largest amounts of cut test score (379 of 400), physical quality (Grade A) and completed SNI No. 2323-2008 requirements with total beans/100 g ratio of 88 beans/100g; pH values of 4,93; acetic acid concentrations of 0,47%, content of fat 15,12%, moisture 4,47%, crude fiber 3,66% and total ash 4,82% after 5 days fermentation., The aimed of this study was to investigate the effect of starter culture addition (Acetobacter aceti, Lactobacillus plantarum, and Saccharomyces cerevisiae) with depulping on the fermentation and quality of cocoa beans. The experimental design of this study was conducted using a 3×5 factorial Completely Randomized Design (CRD) with duplicate replication. The result revealed that starter addition increased ethanol concentration on the fermentation process, increased acetate acid, and citric acid concentration meanwhile oxalic acid was decreased on cocoa beans during 5 days of fermentation. Depulping caused a slight decrease in acetic acid concentration at the end of fermentation with values of 0,47%, meanwhile the sample of cocoa beans without depulping treatment had acetic acid concentration of 0,49%. Starter culture addition and depulping treatment resulted the best characteristic of cocoa beans which visualized by the largest amounts of cut test score (379 of 400), physical quality (Grade A) and completed SNI No. 2323-2008 requirements with total beans/100 g ratio of 88 beans/100g; pH values of 4,93; acetic acid concentrations of 0,47%, content of fat 15,12%, moisture 4,47%, crude fiber 3,66% and total ash 4,82% after 5 days fermentation.]"

"Kusmiyati (2010) Comparasion of iles-iles and cassava tubers as a Saccharomyces cerevisiae substrate fermentation for bioethanol production. Nusantara Bioscience 2: 7-13. The production of bioethanol increase rapidly because it is renewable energy that can be used to solve energy crisis caused by the depleting of fossil oil. The large scale production bioethanol in industry generally usefeedstock such as sugarcane, corn, and cassava that are also required as food resouces. Therefore, many studies on the bioethanol process concerned with the use raw materials that were not competing with food supply. One of the alternative feedstock able to utilizefor bioethanol production is the starchy material that available locally namely iles-iles (Amorphophallus mueller Blum). The contain ofcarbohydrate in the iles-iles tubers is around 71.12 % which is slightly lower as compared to cassava tuber (83,47%). The effect ofvarious starting material, starch concentration, pH, fermentation time were studied. The conversion of starchy material to ethanol havethree steps, liquefaction and saccharification were conducted using α-amylase and amyloglucosidase then fermentation by yeastS.cerevisiaie. The highest bioethanol was obtained at following variables starch:water ratio=1:4 ;liquefaction with 0.40 mL α-amylase(4h); saccharification with 0.40 mL amyloglucosidase (40h); fermentation with 10 mL S.cerevisiae (72h) producing bioethanol 69,81g/L from cassava while 53,49 g/L from iles-iles tuber. At the optimum condition, total sugar produced was 33,431 g/L from cassavawhile 16,175 g/L from iles-iles tuber. The effect of pH revealed that the best ethanol produced was obtained at pH 5.5 duringfermentation occurred for both cassava and iles-iles tubers. From the results studied shows that iles-iles tuber is promising feedstockbecause it is producing bioethanol almost similarly compared to cassava. "

"Pasien yang mengalami defisiensi zink diketahui mengalami penurunan kekebalan tubuh. Hal ini dikarenakan zink berperan dalam respon sel imun. Zink dapat diperoleh diantara lain dari ekstrak khamir (zink-yeast) yang diketahui banyak digunakan sebagai penyedap rasa makanan. Penyerapan dari zink-yeast diketahui lebih baik dibandingkan dengan zink sulfat bila diuji secara in-vivo. Tujuan dari penelitian ini yaitu membuat zink-yeast dengan konsentrasi zink yang optimal, membuat ekstrak khamir yang kaya dengan nukleotida dan isolasi IMP (inosin monofosfat) serta GMP (guanosin monofosfat) dari ekstrak khamir yang berasal dari fermentasi Saccharomyces cerevisiae. Zink-yeast dibuat dengan menambahkan zink sulfat dengan variasi konsentrasi 200, 300 dan 400 μg/mL pada fase stasioner kultur fermentasi khamir dengan media YPD (yeast peptone dextrose). Selanjutnya kandungan zink pada zink-yeast dianalisis dengan metode spektrofotometri serapan atom dan dianalisis kandungan proteinnya dengan metode Bradford. Selain itu, dilakukan pula uji difusi in vitro menggunakan metode sel difusi Franz. Ekstrak khamir yang kaya dengan nukleotida dibuat dengan menggunakan metode hidrolisis enzim dan kemudian dianalisis kadar IMP dan GMP menggunakan metode KCKT pasangan ion dengan detektor PDA pada panjang gelombang 255 nm dengan fase gerak natrium heksan sulfonat-kalium dihidrogen fosfat (90:10) dan laju alir 0,4 ml/menit. IMP dan GMP pada ekstrak khamir lalu diisolasi dengan kromatografi kolom menggunakan fase gerak n- heksan dan etil asetat (1: 2). Hasil zink-yeast terbaik diperoleh pada penambahan 300 μg/mL zink sulfat pada khamir (perolehan atau yield p/s 20,83 %) yang mengandung 2458,30 μg/g zink dan 0,8682 mg/mL protein. Zink-yeast memiliki persen kumulatif difusi zink 39,64% sedangkan zink sulfat diperoleh nilai 2,49%. Pada penelitian ini juga diperoleh 3,2 gram ekstrak khamir yang mengandung kadar IMP 0,25% dan kadar GMP 0,26%. Hasil dari isolasi kromatografi kolom pada ekstrak khamir diperoleh fraksi GMP sejumlah 12,2 mg dan fraksi IMP sejumlah 22,8 mg dengan persen efisiensi purifikasi masing-masing yaitu 52,21% dan 11,92%. Kesimpulan dari penelitian ini yaitu zink-yeast yang optimal diperoleh dengan penambahan 300 μg/mL zink sulfat pada fase stasioner kultur fermentasi khamir. Difusi zink secara in vitro pada zink-yeast lebih baik bila dibandingkan zink sulfat.

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Patients who experience zinc deficiency are known to experience decreased immunity. This is because zinc plays a role in the response of immune cells. Zinc can be obtained among others from yeast extracts (zink-yeast) which are known to be widely used as a flavoring of food. Absorption from zinc-yeast is known to be better than zinc sulfate when tested in vivo. The purpose of this research was to create zinc-yeast with optimal zinc concentration, to make yeast extract enriched with nucleotides, also isolate IMP (inosine monophosphate) and GMP (guanosine monophosphate) from yeast extract derived from the fermentation of Saccharomyces cerevisiae. Zinc-yeast is made by adding zinc sulfate with various concentrations of 200, 300, and 400 μg/mL to the stationary phase of yeast fermentation culture with YPD (yeast peptone dextrose) media. Furthermore, the zinc content in zinc-yeast was analyzed by atomic absorption spectrophotometry and protein content was analyzed by the Bradford method. In addition, in vitro diffusion study was conducted using the Franz diffusion cell method. Yeast extract enriched nucleotide is made using enzyme hydrolysis method and then analyzed for the content of IMP and GMP using the ion pair HPLC method with PDA detector at a wavelength of 255 nm with sodium hexane sulfonate-potassium dihydrogen phosphate (90:10) as mobile phase and flow rate. 0.4 ml/min. IMP and GMP in yeast extract were isolated by column chromatography using n-hexane and ethyl acetate as mobile phase (1: 2). The optimum zinc-yeast results were obtained by adding 300 g/mL zinc sulfate to yeast (yield p/s 20.83%) that contained 2458.30 μg/g zinc and 0.8682 mg/mL protein. Zinc-yeast has a cumulative percent of zinc diffusion of 39.64% while zinc sulfate has a value of 2.49%. This study also obtained 3.2 g of yeast extract containing 0.25% IMP and 0.26% GMP. The results of the isolation of column chromatography on yeast extracts obtained a GMP fraction of 12.2 mg and an IMP fraction of 22.8 mg with the percent purification efficiency is 52.21% and 11.92%, respectively. This study concludes that the optimal zinc-yeast was obtained by adding 300 μg/mL of zinc sulfate in the stationary phase of yeast fermentation culture. In vitro zinc diffusion in zinc-yeast is better than zinc sulfate."

"ABSTRAKCocopeat serat kelapa dan sampah daun kering biasanya tidak mempunyai nilai jual. Kandungan dari kedua biomassa seperti lignin, selulosa, hemiselulosa dan kandungan bisa dimanfaatkan menjadi etanol dengan bantuan bakteri Zymomonas mobilis untuk proses fermentasi dan selulosa untuk proses hidrolisis. Proses produksi etanol melalui tiga tahap yaitu delignifikas, hidrolisis, dan fermentasi. Pengukuran absorbansi dilakukan untuk melihat pertumbuhan bakteri Zymomonas mobilis dan selulosa. Absorbansi tertinggi Zymomonas mobilis pada hari ke 4 yaitu 2.336 dan selulosa pada hari ke 3 sebesar 0.217. Absorbansi yang tinggi menghasilkan kecepatan produksi alkohol yang maksimum. Kadar alkohol yang paling tinggi pada biomassa 15 gram Cocopeat adalah 0.3701 dan sampah daun kering sebesar 0.2957.

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ABSTRACTCocopeat coconut fiber and dry leaf litter usually do not have marketable value . The content of the biomass such as lignin, cellulose, hemicellulose, and the content can be utilized to ethanol by Zymomonas mobilis bacteria for fermentation and hydrolysis of cellulose to process. The ethanol production process through three stages delignification, hydrolysis, and fermentation. Absorbance measurement was conducted to see the growth of bacteria Zymomonas mobilis and cellulose. The highest absorbance Zymomonas mobilis on day 4, namely 2.336 and cellulose on day 3 of 0.217. High absorbance generate maximum speed of alcohol production. The most high alcohol have 15 gram content to Cocopeat is 0.3701 and the dry leaf litter at 0.2957 ."

"Berbagai penyakit dalam tubuh disebabkan oleh adanya radikal bebas. Radikal bebas adalah atom atau gugus yang memiliki satu atau lebih elektron tidak berpasangan. Dalam melindungi tubuh dari serangan radikal bebas, substansi antioksidan berfungsi untuk menstabilkan radikal bebas dengan melengkapi kekurangan elektron dari radikal bebas, sehingga menghambat terjadinya reaksi berantai. Buah manggis merupakan hasil pertanian pangan yang melimpah di Indonesia, dengan produksi lebih dari 190 ribu ton manggis setiap tahunnya. Kulit buah manggis memiliki kandungan senyawa polifenol cukup tinggi yang berperan sebagai antioksidan, namun belum banyak dimanfaatkan. Proses fermentasi merupakan salah satu cara efektif untuk memanfaatkan limbah kulit buah manggis untuk memproduksi antioksidan guna menangkal radikal bebas yang masuk ke dalam tubuh. Khamir Saccharomyces cerevisiae terbukti dapat meningkatkan kadar antioksidan buah melalui fermentasi. Tujuan dari penelitian ini adalah menentukan suhu fermentasi, pH fermentasi, lama waktu fermentasi dan konsentrasi biomassa kulit buah manggis (Garcinia mangostana Linn) dengan khamir Saccharomyces cerevisiae yang optimum untuk menghasilkan aktivitas antioksidan terbaik. Konsentrasi biomassa kulit buah manggis divariasikan menggunakan metode OVAT (One Variable at A Time), sedangkan suhu fermentasi, pH fermentasi dan lama waktu fermentasi dioptimasi menggunakan RSM (Response Surface Methodology). Sampel hasil fermentasi kemudian dilakukan pengujian antara lain uji TPC (Total Phenolic Content), TFC (Total Flavonoid Content) berikut dengan analisisnya menggunakan software Design-Expert 11, dan uji DPPH (Difenil-2-Pikrilhidrazil) guna mengetahui aktivitas antioksidan melalui senyawa polifenol. Kemudian dilakukan karakterisasi untuk menentukan komposisi antioksidan menggunakan pendekatan LC-MS (Liquid Chromatography-Mass Spectroscopy). Hasil penelitian menunjukkan bahwa kondisi operasi terbaik untuk menghasilkan aktivitas antioksidan optimum sebesar 5,68 ppm antioksidan adalah pada suhu 31,5oC, pH 6, waktu 6 jam dan konsentrasi bubuk kulit manggis 20%. Senyawa Alpha-mangostin atau 1,3,6-Trihydroxy-7-methoxy-2,8-bis(3-methylbut-2-en-1-yl)-9H-xanthen-9-one merupakan senyawa dengan komposisi tertinggi baik pada sampel fenolik maupun flavonoid.

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Various diseases in the body are caused by the presence of free radicals. Free radicals are atoms or groups that have one or more unpaired electrons. In protecting the body from free radical attack, antioxidant substances function to stabilize free radicals by complementing the lack of electrons from free radicals, thereby inhibiting chain reactions. Mangosteen fruit is an abundant agricultural food product in Indonesia, with a production of more than 190 thousand tons of mangosteen each year, this is directly proportional to the abundant amount of mangosteen rind waste. Mangosteen rind contains quite high polyphenols compounds which act as antioxidants, but have not been widely used. The fermentation process is one of the most effective ways to utilize mangosteen rind waste to produce antioxidants to ward off free radicals that enter the body. One of the most widely used microorganisms in fermentation is Saccharomyces cerevisiae because besides being cheap, easier to obtain, and commonly used in the production of food and beverage industries, Saccharomyces cerevisiae yeast is proven to increase fruit antioxidant levels through fermentation. The purpose of this study are to determine the optimum fermentation temperature, fermentation pH, fermentation time, and biomass concentration of mangosteen rind (Garcinia mangostana Linn) with yeast (Saccharomyces cerevisiae) to produce the best antioxidant activity. The concentration of mangosteen rind biomass will be vary using the OVAT (One Variable at A Time) method, while fermentation temperature, pH fermentation, and fermentation time will be optimized using RSM (Response Surface Methodology). The sample of fermentation then will carry out by some tests, among others TPC (Total Phenolic Content), TFC (Total Flavonoid Content) along with the analysis using the Design-Expert 11 software, and DPPH (Difenil-2-Pikrilhidrazil) test to determine antioxidant activity through polyphenol compounds. Then carry out characterization to determine the composition of antioxidant using the LC-MS (Liquid Chromatography-Mass Spectroscopy) approach. The result showed that the best operating condition to produce the optimum antioxidant activity of 5,68 ppm antioxidant was at a temperature of 31,5oC, pH 6, time of 6 hours and a concentration of 20% mangosteen peel powder. Alpha-mangostin or 1,3,6-Trihydroxy-7-methoxy-2,8-bis(3-methylbut-2-en-1-yl)-9H-xanthen-9-one compound was the compound with the highest composition both at phenolic and flavonoid samples."

"Commercialization of bioethanol has recently intensified due to its market stability, low cost,sustainability, alternative fuel energy composition, greener output and colossal fossil fuel depletion. Recently, because of greenhouse intensity worldwide, many researches are ongoing to reprocess the waste as well as turning down the environmental pollution. With this scenario, the invention of bioethanol was hailed as a great accomplishment to transform waste biomass to fuel energy and in turn reduce the massive usages of fossil fuels. In this study, our review enlightens various sources of plant-based waste feed stocks as the raw materials for bio ethanol production because they do not adversely impact the human food chain. However, the cheapest and conventional fermentation method, yeast fermentation is also emphasized here notably for waste biomass-to-bio ethanol conversion. Since the key fermenting agent, yeastis readily available in local and international markets, it is more cost-effective in comparison with other fermentation agents. Furthermore, yeasthas genuine natural fermentation capability biologically and it produces zero chemical waste. This review also concerns a detailed overview of the biological conversion processes of lignocellulosic waste biomass-to-bio ethanol, the diverse performance of different types of yeasts and yeast strains, plus bioreactor design, growth kinetics of yeast fermentation, environmental issues, integrated usages on modern engines and motor vehicles, as well as future process development planning with some novel co-products."

"Tokotrienol merupakan vitamin E tak jenuh yang memiliki bioaktivitas yang unggul. Tokotrienol dapat digunakan sebagai antioksidan, antikanker, agen neuroprotektif, dan penurun kolesterol. Salah satu sumber alami tokotrienol adalah bekatul. Bekatul merupakan produk samping yang terbuang selama proses penyosohan beras. Pengayaan senyawa bioaktif pada minyak bekatul dapat dilakukan dengan fermentasi padat menggunakan kapang Aspergillus terreus. Penelitian ini memvariasikan volume inokulum kapang yang ditambahkan pada proses fermentasi sebesar 1; 3; 5; 7; dan 9 mL untuk menentukan volume inokulum optimum yang menghasilkan kadar tokotrienol maksimum. Volume inokulum berpengaruh pada hasil metabolisme kapang dalam meningkatkan senyawa bioaktif pada minyak bekatul yang difermentasi. Hasil uji minyak bekatul menggunakan spektrofotometer UV-Vis didapatkan volume inokulum optimum sebesar 5 mL dengan perolehan tokotrienol 4509,91 ppm. Senyawa bioaktif lainnya yang memiliki aktivitas antioksidan yang terdapat pada minyak bekatul dianalisis menggunakan GC-MS. Sejumlah senyawa yang teridentifikasi yaitu asam pentadekanoat, 14-metil-, metil ester (C₁₇H₃₄O₂), asam heksadekanoat (C₁₆H₃₂O₂), asam 9-dodekenoat metil ester (C₁₃H₂₄O₂), dan asam oleat (C_18­H₃₄O₂).

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Tocotrienols are unsaturated vitamin E with superior bioactivity. Tocotrienols can be used as antioxidants, anticancer, and neuroprotective and cholesterol-lowering agents. One of the natural sources of tocotrienols is rice bran. Rice bran is a by-product that is wasted during the milling process of rice. Enrichment of bioactive compounds in rice bran oil can be done by solid-state fermentation using the mold Aspergillus terreus. This study varied the volume of mold inoculum added to the fermentation process by 1; 3; 5; 7; and 9 mL to determine the optimum inoculum volume that produces maximum tocotrienol content. The volume of inoculum affects the results of mold metabolism in enriching bioactive compounds in fermented rice bran oil. The results of the rice bran oil test using spectrophotometer UV-Vis obtained an optimum inoculum volume of 5 mL with a tocotrienol content of 4509.91 ppm. Other bioactive compounds that have antioxidant activity in rice bran oil were analyzed using GC-MS. The identified compounds are pentadecanoic acid, 14-methyl-, methyl ester (C₁₇H₃₄O₂), hexadecenoic acid (C₁₆H₃₂O₂), 9-dodecenoic acid methyl ester (C₁₃H₂₄O₂), and oleic acid (C_18­H₃₄O₂)."

"Minyak bekatul mengandung asam lemak tak jenuh yang sangat potensial untuk mencegah dan menurunkan risiko hiperkolesterolemia. Hiperkolesterolemia adalah suatu kondisi meningkatnya konsentrasi kolesterol dalam darah yang melebihi nilai normal. Kondisi ini dapat dicegah dengan mengonsumsi asam lemak tak jenuh, seperti asam linoleat (C18:2). Efek hipokolesterolemik yang dimiliki oleh minyak bekatul dapat menurunkan kadar kolesterol dalam darah sehingga mengurangi risiko penyakit arterosklerosis dan jantung koroner. Bekatul adalah substrat paling efektif untuk memproduksi asam lemak jenis tersebut. Fermentasi bekatul menggunakan kapang Aspergillus terreus merupakan salah satu cara untuk menjaga dan memperkaya kandungan asam lemak tak jenuh dalam minyak bekatul. Kapang Aspergillus terreus mampu memproduksi minyak yang mempunyai komposisi asam lemak tak jenuh yang lebih tinggi dibandingkan dengan spesies Aspergillus lainnya. Penelitian ini mengkaji pengaruh waktu inkubasi kapang untuk mengetahui kandungan asam lemak tak jenuh dalam minyak bekatul hasil fermentasi. Metode fermentasi yang digunakan adalah fermentasi padat dengan metode ekstraksi Bligh-Dyer termodifikasi. Gas Chromatography/Mass Spectrometry (GC/MS) adalah instrumen yang digunakan untuk mengetahui komposisi dan kandungan dari asam lemak tak jenuh dalam minyak bekatul. Hasil penelitian menunjukkan bahwa waktu inkubasi untuk pengayaan asam linoleat dalam minyak bekatul dengan menggunakan Aspergillus terreus, yaitu selama 6 hari dengan kandungan asam linoleat semula 37,758% menjadi 39,780%.

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Rice bran oil contains unsaturated fatty acids which are very potential to prevent and reduce the risk of hypercholesterolemia. Hypercholesterolemia is a condition of increasing concentration of cholesterol in the blood that exceeds the normal value. This condition can be prevented by consuming unsaturated fatty acids, such as linoleic acid (C18:2). Hypocolesterolemic effects possessed by rice bran oil can reduce blood cholesterol levels thereby reducing the risk of atherosclerosis and coronary heart disease. Rice bran is the most effective substrate for producing that type of fatty acids. Its fermentation using Aspergillus terreus mold is one of the ways to maintain and enrich the unsaturated fatty acid content in rice bran oil. Aspergillus terreus can produce oil that has a higher composition of unsaturated fatty acids compared to another Aspergillus species. This study examines the effect of incubation time of mold inoculum to determine the content of unsaturated fatty acids in fermented bran oil. The fermentation method used is solid fermentation using the modified Bligh-Dyer extraction method. Gas Chromatography/Mass Spectrometry (GC/MS) is an instrument which is used to determine the composition and content of unsaturated fatty acids in rice bran oil. The result showed that the incubation time for the enrichment of linoleic acid in rice bran oil using Aspergillus terreus, which is for 6 days with linoleic acid content of originally 37,758% to 39,780%."

"Indonesia memiliki ketergantungan yang cukup tinggi terhadap bahan bakar fosil dalam pemenuhan kebutuhan energi. Akan tetapi, penurunan ketersediaan bahan bakar fosil membuat perlunya pengembangan energi terbarukan, salah satunya adalah biobutanol. Biobutanol adalah sumber energi alternatif yang sangat potensial karena tidak menyebabkan korosi, tidak menyerap air, dan mempunyai angka oktan yang hampir sama dengan bensin. Biobutanol dihasilkan dari fermentasi sederhana secara anaerob oleh bakteri Clostridium beijerinckii yang dapat merubah berbagai macam monosoakarida menjadi aseton, butanol, dan etanol (ABE). Pada penelitian ini, sumber glukosa diperoleh dari kertas. Kertas dihidrolisis dengan menggunakan dua metode, yaitu menggunakan H2SO4 1% dan kombinasi enzim (selulase, selobiase, silanase). Hasil hidrolisis difermentasi secara anaerob selama 72 jam pada suhu 370C. Butanol yang dihasilkan adalah sebanyak 0,0000295 ml/gram kertas.

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Indonesia is highly dependent on fossil fuels to fulfill energy needs. However, availability of fossil fuel resources is decreasing. This has stimulated the development of alternative renewable resources to substitute fossil fuels, for example biobutanol. Biobutanol is an alternative energy source with huge potential because it does not cause corrosion, non-hygroscopic, and has similiar octane number as gasoline. Biobutanol is produced from anaerobic fermentation using Clostridium beijerinckii bacteria that can change various monosoakarida into acetone, butanol, and ethanol (ABE).

In this sudy, the source of glucose obtained from paper. Paper hydrolized by using two methods, using 1% H2SO4 and combinations of enzymes (cellulase, cellobiase, xylanase). Hydrolysis results is fermented in anaerobic chamber for 72 hours at temperature 370C. The result of butanol production is 0.0000295 ml/gram paper."