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"[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.]"

"Fosfor (P) merupakan salah satu mineral dalam limbah kotoran manusia yang kurang dimanfaatkan. Tidak ada prioritas global untuk memastikan aksesibilitas fosfor yang cukup di masa mendatang sehingga perlu adanya pemulihan atau daur ulang fosfor, salah satunya ialah melalui proses fermentasi secara anaerobik untuk dipergunakan kembali sebagai produk agrikultur berupa pupuk. Dalam pengolahan anaerobik, proses fermentasi akan menghasilkan produk berupa volatile fatty acid (VFA) yang dapat diaplikasikan dalam produksi bioplastik, bioenergi, dan penyisihan nutrien dari limbah. Penelitian ini bertujuan untuk mengidentifikasi pelepasan fosfor dan produksi VFA dari lumpur tinja melalui proses fermentasi. Penelitian didahului dengan pengujian ICP-OES untuk mengidentifikasi karakteristik lumpur tinja, kemudian proses fermentasi dilakukan dengan menggunakan reaktor batch selama delapan (8) hari. Hasil eksperimen menunjukkan bahwa kondisi optimum pelepasan fosfor dan produksi VFA berada pada hari ke-8 fermentasi dengan perolehan konsentrasi fosfor terlarut sebesar 52,02 mg/L, persentase P-release sebesar 6%, dan konsentrasi VFA sebesar 1.351,35 mg/L. Pelepasan fosfor dipengaruhi oleh keberadaan bakteri asidogenik dalam reaktor dapat melepaskan fosfor sekaligus memproduksi VFA. Produksi VFA dan pH, kandungan logam berat, serta bahan organik kompleks juga memengaruhi pelepasan fosfor seiring berjalannya proses fermentasi yang terbukti dengan adanya tren peningkatan dan penurunan konsentrasi fosfor selama penelitian berlangsung.

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Phosphorus (P) is one of the underutilized minerals in human waste. There is no global priority to ensure sufficient phosphorus accessibility in the future, necessitating phosphorus recovery or recycling. One method for this is through anaerobic fermentation to be reused as agricultural products like fertilizers. In anaerobic treatment, the fermentation process also produces volatile fatty acids (VFAs), which can be applied in the production of bioplastics, bioenergy, and nutrient removal from waste. This study aims to identify phosphorus release and VFA production from fecal sludge through fermentation. The study began with ICP-OES testing to identify the characteristics of fecal sludge, followed by an eight-day batch reactor fermentation process. The experimental results showed that the optimal conditions for phosphorus release and VFA production were on the 8th day of fermentation, with a dissolved phosphorus concentration of 52.02 mg/L, a P-release percentage of 6%, and a VFA concentration of 1,351.35 mg/L. Phosphorus release was influenced by the presence of acidogenic bacteria in the reactor, which release phosphorus while producing VFAs. VFA production, pH, heavy metal content, and complex organic matter also affected phosphorus release throughout the fermentation process, as evidenced by the trends of increasing and decreasing phosphorus concentrations observed during the study."

"Etanol atau bioetanol adalah senyawa alkohol berantai karbon dua yang bermanfaat sebagai pelarut organik dan antiseptik dalam dunia farmasi dan kesehatan. Selain itu etanol menjadi salah satu solusi bagi permasalahan krisis energi dunia. Bioetanol dibuat dengan fermentasi menggunakan khamir Saccharomyces cerevisiae. Proses ini mengubah rantai berkarbon enam, glukosa sebagai sumber substratnya, menjadi rantai berkarbon dua yaitu etanol. Sumber dari rantai berkarbon enam dapat diambil dari limbah biomassa Tandan Kosong Kelapa Sawit (TKKS) yang mengandung selulosa, hemiselulosa dan lignin. Tujuan dari penelitian ini adalah menemukan khamir potensial penghasil bioetanol dan mendapatkan kondisi fermentasi optimum yang dipengaruhi oleh pengadukan, suhu, detoksifikasi hidrolisat, dan konsentrasi sumber N pada media. Isolasi khamir potensial dilakukan dari lima jenis buah yang berbeda yaitu Anggur Merah, Anggur Hitam, Durian Medan, Durian Bangkok dan Durian Montong. Dari isolat-isolat yang didapatkan, isolat DM1 yang diperoleh dari Durian Medan cukup potensial menghasilkan bioetanol, namun masih lebih rendah dari Saccharomyces cerevisiae pembanding. Hasil analisis kromatografi gas menunjukan bahwa kondisi terpilih dalam fermentasi bioetanol yaitu pada kondisi temperatur lebih rendah di bawah suhu kamar (+220C), tanpa pengadukan, menggunakan hidrolisat tanpa detoksifikasi, dengan konsentrasi amonium asetat sebagai sumber N sebesar 1%. Konsentrasi bioetanol yang dihasilkan adalah 0,241%.

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Ethanol or bioethanol is a two-carbon chain alcohol compound that are useful as an organic solvent and antiseptics in pharmaceutical and health. In addition, ethanol can be one of solution to the problem of world energy crisis. Bioethanol is made by fermentation process using yeast Saccharomyces cerevisiae. The processes change the six-carbon chain, as the source of its substrate, into a two-carbon chain, namely ethanol. The source of six-carbon chain can be taken from the waste of biomass Oil Palm Empty Fruit Bunch (EFB), which contains cellulose, hemicellulose and lignin.

The purpose of this research was to find potential yeast producing bioethanol and to obtain optimum fermentation conditions were influenced by effect of shaking, temperature, detoxification of hydrolyzate, and concentration of N sources on media. Isolation of potential yeast was carried out from five different types of fruit, namely Red Grape, Black Grape, Durian Medan, Durian Bangkok and Durian Montong.

Among isolates, Isolate DM1 that obtained from Durian Medan was quite potential to produce bioethanol but still lower than comparator Saccharomyces cerevisiae. Results of analysis using gas chromatography showed that the selected conditions in the fermentation of bioethanol are in temperature conditions below room temperature (+220C), without shaking, using the hydrolyzate without detoxification, with 1% concentration of ammonium acetate as a source of N. The concentration of ethanol produced was 0,241%."

"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."

"This study was focused on the selection of type of beans for kecap production. The mold fermentation or kecap koji making process was conducted in small scale at room temperature for 3 days and the brine fermentation for 2 weeks at room temperature.Product were analyzed for biochemical (total nitrogen, formol nitrogen, and total water soluble nitrogen) content. It was found that the final composision of kecap mash were mainly due to brain fermentation and by activities of strains showed varies effect to total nitrogen (TN), formol nitrogen (FN), and total water soluble nitrogen (WN).Kecap mash produced using kedelai, hiris and tolo inoculated with Aspergillus sp. K-1 containing formol nitrogen 0.58%, 0.65% and 0.57%, respectively.Meanwhile using Aspergillus sp. K-1A producing kecap mash with formol nitrogen were 0.75%, 0.75%, 0.65%, respectly. The ratio of WN to TN of the kecap mash from hiris and tolo were up to 50%, while the ratio of FN to TN varies, which was influenced by the koji used.Based on the chemical properties above, it can be recommended that hiris can be used for kecap production though requires extensive researches."

"Rhizopus oryzae is known to produce lactic acid, protease and lipase, make it potential as a starter in cheese production. However, R. oryzae application in the unripened cheese production has not been elucidated. In this research, microbiology and nutritional status of unripened cheese fermented by R. oryzae was analyzed and compared to that of the cheese made by rennet as a control. total plate count of bacteria in unripened cheese fermented by R. oryzae was 8.1 X 10 cfu/ml in PCA medium and 3.7 X 10 cfu/ml in MRSA. Total count of funig group was conducted using PDA, resulting 1.2 X 10 cfu/ml. Dominant microflora were identified as enterococcus faecalis and bacillus subtilis in MRSA and Aspergillus sp. in PDA. HPLC analysis of the unripened cheese fermented by R. oryzae showed that in had higher essential amino acid content than the control. The essential amino acid found were Threonine (1,15 ppm), L-Methionine (0,47 ppm), L-Valine + L-Tryptophan (0,70 ppm), L-Phenylalanine (0,66 ppm), L-Isoleucine (0,48 ppm), L-Leucine (1,28 ppm), and L-Lycine (1,64 ppm)."

"The volatile chemicals from species of wild Cinnamomum spp. (C. racemosum, C. cuspidatum, C. politum, C. javanicum), Etlingera spp. (E. pyramidosphaera, E. megalocheilos, E. coccinea, E. elatior) and Schizostachyum spp. (S. blumei, S. brachycladum, S. lima, S. pilosum) found in Sabah were investigated. The oils were obtained from the bark, rhizome and culm of respective specimens by hydrodistillation and the profile of volatile chemicals was obtained using Gas Chromatography- Mass Spectrometry (GCMS). Dominance of eucalyptol, terpinen-4-ol and eugenol were consistent among the species from genus Cinnamomum. aromadendrane oxide, lauryl aldehyde, elemicin, borneol and 1-dodecanol were predominant among the species from genus Etlingera. α-elemol, coumaran, guiacol-4-vinyl, palmitic acid and phytol acetate predominate the species from genus Schizostachyum. Strong inhibition against Staphylococcus aureus (MIC: 5.62 ± 0.5 μg mL-1) were exhibited by essential oils of C. cuspidatum and E. coccinea, oil of S. blumei inhibited Listeria monocytogenes (MIC: 4.60 ± 0.5 μg mL-1), oil of C. javanicum inhibited Salmonella typhimurium (MIC: 5.50 ± 0.5 μg mL-1). meanwhile the oil of C. politum suppressed Salmonella enteritidis (MIC: 5.20 ± 0.5 μg mL-1) was measured using microdilution method. these findings reveal the potential of selected plants used by indigenous communities of Borneo as antimicrobials in food, cosmetics and pharmaceutical industries."

"ABSTRAKThe volatile chemicals from species of wild Cinnamomum spp. (C. racemosum, C. cuspidatum, C. politum, C. javanicum), Etlingera spp. (E. pyramidosphaera, E. megalocheilos, E. coccinea, E. elatior) and Schizostachyum spp. (S. blumei, S. brachycladum, S. lima, S. pilosum) found in Sabah were investigated. The oils were obtained from the bark, rhizome and culm of respective specimens by hydrodistillation and the profile of volatile chemicals was obtained using Gas Chromatography- Mass Spectrometry (GCMS). Dominance of eucalyptol, terpinen-4-ol and eugenol were consistent among the species from genus Cinnamomum. aromadendrane oxide, lauryl aldehyde, elemicin, borneol and 1-dodecanol were predominant among the species from genus Etlingera. α-elemol, coumaran, guiacol-4-vinyl, palmitic acid and phytol acetate predominate the species from genus Schizostachyum. Strong inhibition against Staphylococcus aureus (MIC: 5.62 ± 0.5 μg mL-1) were exhibited by essential oils of C. cuspidatum and E. coccinea, oil of S. blumei inhibited Listeria monocytogenes (MIC: 4.60 ± 0.5 μg mL-1), oil of C. javanicum inhibited Salmonella typhimurium (MIC: 5.50 ± 0.5 μg mL-1). meanwhile the oil of C. politum suppressed Salmonella enteritidis (MIC: 5.20 ± 0.5 μg mL-1) was measured using microdilution method. these findings reveal the potential of selected plants used by indigenous communities of Borneo as antimicrobials in food, cosmetics and pharmaceutical industries."