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"Enzim kolesterol oksidase adalah enzim oksidoreduktase yang mampu mendegradasi kolesterol. Pada percobaan ini, dilakukan produksi enzim kolesterol oksidase oleh Streptomyces sp. melalui fermentasi submerged lalu dilakukan investigasi terhadap aktivitas dan kemampuan katalisis enzim kolesterol oksidase. Pada percobaan, substrat dan enzim divariasikan pada berbagai konsentrasi, yaitu 0,15, 0,075, dan 0,0375 U/mL dan 1,25, 2,5, dan 5 mg/mL. Perbandingan konstanta laju reaksi antara ekstrak kasar enzim dan enzim komersial diperoleh dari hasil penelitian. Perbandingan konstanta laju reaksi enzimatis oleh faktor yang mempengaruhi, diantaranya imobilisasi enzim dan suhu inkubasi enzim, dengan data yang diperoleh dari literatur. Enzim dan substrat mengalami reaksi oksidasi pada waktu inkubasi 5, 30, 65, 120, dan 240, lalu konsentrasi kolesterol residu pada sampel dilakukan plotting dengan waktu inkubasi, dan konstanta laju reaksi diperoleh melalui permodelan reaksi orde 1 dengan pendekatan integrasi numerik Euler. Aktivitas ekstrak kasar enzim yaitu 1,69 U/mL dengan konstanta laju reaksi yaitu 0,01/menit untuk ekstrak kasar enzim dan 0,014/menit untuk enzim komersial. Selanjutnya, diperoleh faktor yang mempengaruhi konstanta laju reaksi oksidasi kolesterol secara enzimatik oleh enzim kolesterol oksidase, yaitu konsentrasi enzim, jenis enzim, imobilisasi, dan suhu inkubasi. Reaksi oksidasi kolesterol oleh enzim kolesterol oksidase dari Streptomyces sp. mengikuti reaksi orde 1.

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Cholesterol oxidase well known as oxidoreductase enzyme which able to degrade the cholesterol. Here, we produced cholesterol oxidase from Streptomyces sp. by submerged fermentation and investigate the activity and cholesterol oxidation kinetics of cholesterol oxidase. The enzyme and substrate are diluted in various concentration, 0.15, 0.075, 0.0375 U mL and 1.25, 2.5, 5 mg mL, respectively. Further step was comparing crude enzyme and commercial enzyme from Streptomyces sp. by oxidation constant rate of reaction. The enzyme and substrate were through the oxidation reaction, and the amount of cholesterol residue in the sample are determined by HPLC. In this work, we also compared the oxidation constant rate of reaction of previous experiment from literature with affecting factors, such as immobilization and incubating temperature. The cholesterol residue in the sample are plotted by time reaction and the rate constant is obtained by first order rate reaction using Euler integration method. The crude enzyme activity is 1.69 U mL and the reaction constant are 0.01 U mL and 0.014 for crude extract and commercial enzyme, respectively. Furthermore, several factors affecting constant rate of enzymatic oxidation of cholesterol were enzyme concentration, enzyme type, immobilization, and incubating temperature. Cholesterol oxidation by Streptomyces sp. cholesterol oxidase was follow the first order reaction."

"Plastik yang banyak digunakan saat ini bersifat nonbiodegradable, sehingga limbah plastik menjadi sulit dihancurkan dan menjadi polutan. Upaya untuk mengatasi masalah limbah plastik adalah dengan membuat material plastik yang mudah diuraikan oleh alam. Polyhydroxybutyrate (PHB) adalah salah satu jenis plastik biodegradable yang ramah lingkungan. PHB dapat dihasilkan oleh bakteri pada saat fermentasi. Pada penelitian ini proses fermentasi menggunakan bakteri Bacillus cereus strain suaeda B-001. Sumber karbon yang digunakan dalam fermentasi adalah glukosa murni dan hidrolisat tandan kosong kelapa sawit (TKKS). TKKS diubah menjadi gula reduksi melalui proses hidrolisis asam. Selanjutnya pembentukkan PHB dengan fermentasi menggunakan hidrolisat TKKS sebagai sumber karbon. Kemudian ekstraksi PHB dari dalam sel biomass untuk mendapatkan PHB murni. Hasil penelitian pada sumber karbon glukosa murni 15 g/L mendapatkan berat sel kering (CDW) sebesar 2,62 g/L dan kadar PHB sebesar 43,1 %CDW. Sedangkan pada sumber karbon hidrolisat TKKS 14,3 g/L menghasilkan berat sel kering sebesar 2,5 g/L dan kadar PHB 40 %CDW. Hasil analisa FTIR dan H NMR terhadap produk PHB menunjukkan gugus fungsi dan struktur yang mirip dengan PHB standart. Hasil analisis dengan DSC didapatkan PHB mempunyai titik leleh pada 171,52 oC, temperatur transisi pada -17,37 oC dan ΔH sebesar 105,16 J/g.

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The effort to overcome the problem of plastic waste is to make plastic material that is easily broken down by nature. Polyhydroxybutyrate (PHB) is one type of biodegradable plastic that is environmentally friendly. PHB can be produced by bacteria during fermentation.

In this study the fermentation process uses Bacillus cereus strain suaeda B-001. The carbon sources used in fermentation are pure glucose and oil palm empty fruit bunches (OPEFB) hydrolyzates. OPEFB is converted into reducing sugars through an acid hydrolysis process. Furthermore, the formation of PHB by fermentation using OPEFB hydrolyzate as a carbon source. Then extraction of PHB from biomass cells to obtain pure PHB.

The results of experiment using 15 g/L of pure glucose as a carbon source obtained dry cell weight (CDW) of 2.62 g/L and accumulated PHB of 43.1% CDW. Whereas if using OPEFB hydrolyzate 14.3 g / L as a carbon source produced CDW of 2.5 g/L and accumulated PHB of 40% CDW. The results of FTIR and H NMR analysis of PHB products show functional groups and structures similar to standard PHB. Analysis with DSC found the melting point of PHB at 171.52 oC, the transition temperature of PHB at -17.37 oC and PHB had ΔH 105.16 J/g."

"Fermentasi asam suksinat dari tandan kosong kelapa sawit (TKKS) menggunakan bakteri amobil dari rumen sapi saat ini sedand diteliti. TKKS adalah salah satu bahan baku yang dapat digunakan untuk produksi asam suksinat karena memiliki kandungan glukosa, harga rendah, serta tersedia banyak di alam. Asam suksinat dapat diproduksi dengan beberapa metode seperti fermentasi yang dianggap lebih ramah lingkungan karena mengkonsumsi CO₂ selama prosesnya sehingga berkontribusi pada pengurangan emisi CO₂. Bakteri yang digunakan dalam percobaan ini diisolasi dari rumen sapi dan akan diimobilisasi sebelum masuk ke proses produksi asam suksinat. Fermentasi dilakukan dengan teknik Semi Simurrentous Saccharification and Fermentation (SSSF). Hidrolisis dilakukan dengan menggunakan enzim selulase selama 2 - 6 jam sebelum fermentasi terjadi. Yeast extract sebagai sumber nitrogen dan MgCO₃ sebagai zat pengatur pH divariasikan kemudian akan hasil fermentasi berupa konsentrasi asam suksinat, yield, dan produktivitas akan dibandingkan. Fermentasi dilakukan selama 48 jam dalam water bath shaker dan suhunya dijaga pada suhu 37^oC. Produk fermentasi akan dianalisis menggunakan HPLC untuk mengetahui kandungan asam suksinat. Kondisi fermentasi optimal untuk produksi asam suksinat didapatkan saat: waktu hidrolisis - 6 jam, sumber pH awal - 20 g/L, konsentrasi agen pengatur pH awal - 20 g/L. Pada kondisi yang dioptimalkan ini, produksi maksimum asam suksinat ditemukan menjadi 1,43 g/L dengan hasil asam suksinat dengan konsentrasi glukosa awal dan 0,0297 g/L. produktivitas.

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The fermentation of succinic acid from oil palm empty fruit bunches (EFB) using immobilized bacteria from cow rumen were investigated. EFB is one of raw material that can be used for succinic acid production due to its cellulose content, low prices, and availability. Succinic acid can be produced effectively by several methods, one of them is fermentation which considered more environmentally friendly due to CO₂ consumed during the process, thereby potentially contributing to reduction of CO₂ emission. Bacteria used in this experiment were isolated from cow rumen which must be immobilized before getting into succinic acid production process.

Fermentation is done by Semi Simultaneous Saccharification and Fermentation (SSSF) technique. Saccharification was carried out using cellulase enzyme for 2 – 6 hours before fermentation occurs. Yeast extract as nitrogen sources and MgCO₃ as pH regulating agent were varied and compared in terms of product concentration, yield, and productivity. Fermentation was carried out for 48 hours in shaker water bath and the temperature maintained at 37^oC. Fermentation product was then examined using HPLC to find out the succinic acid content.

The optimum fermentation conditions for succinic acid production were found to be: saccharification time – 2 hours, initial nitrogen sources concentration – 20 g/L, initial pH regulating agent concentration – 20 g/L. At these optimized condition, the maximum production of succinic acid was found to be 1.47 g/L with 19.64 g/g yield of succinic acid to initial glucose concentration and 0.03 g/L.h productivity."

"Although technological advances have fueled the rising demand for lipase as a biocatalyst, commercial availability remains limited and costs prohibitive. To meet this need, an extracellular lipase enzyme from Aspergillus niger can be produced through solid state fermentation (SSF) using agroindustrial wastes including tofu dregs, coconut dregs, and corn bran. These agroindustrial residues still contain nutrients, especially lipids/triglycerides, making them a potential fermentation medium to produce lipase. Lipase with the highest activity level (8.48 U/mL) was obtained using a tofu dreg substrate, 4% inducer concentration, and 9-day fermentation period. This crude lipase extract was then dried with a spray drier and immobilized in a macroporous anion resin using the adsorption-crosslinking method. The immobilized lipase’s activity was assayed by a biodiesel synthesis reaction; it showed 48.3% yield. The immobilized enzyme's stability was also tested through four cycles of biodiesel synthesis; in the fourth cycle, the enzyme maintained 84% of its initial activity."

"Tokotrienol adalah anggota dari keluarga vitamin E dengan sifat neuroprotektif, antioksidan, antikanker, dan penurun kolestrol. Salah satu sumber dari senyawa tokotrienol adalah bekatul. Tokotrienol tersebut dapat diperoleh dari minyak bekatul yang merupakan salah satu minyak nabati dengan kandungan tokotrienol tertinggi. Untuk memperkaya kadar tokotrienol dalam minyak bekatul, dilakukan fermentasi pada bekatul dengan kapang Aspergillus terreus. Penelitian ini mengamati pengaruh variasi rasio pelarut metanol:kloroform:air dan fermentasi dengan kapang Aspergillus terreus saat melakukan proses ekstraksi terhadap peningkatan perolehan tokotrienol dalam minyak bekatul. Pada penelitian ini, dilakukan solid state fermentation pada bekatul sebelum minyak bekatul diekstraksi dengan metode Bligh-Dyer dan dianalisis dengan instrumen spektrofotometri UV dan GC/MS untuk mengetahui kadar tokotrienol dalam minyak bekatul. Hasil penelitian ini menunjukkan bahwa rasio pelarut metanol:kloroform:air terbaik untuk peningkatan perolehan tokotrienol hasil ekstraksi adalah pada rasio metanol:kloroform:air 1:1:0,9 (v/v/v), dengan peningkatan perolehan konsentrasi tokotrienol dari 2541,44 ppm menjadi  3642,79 ppm, dan proses fermentasi meningkatkan kadar tokotrienol dalam minyak bekatul dari 2541,44 ppm menjadi 3257,66 ppm. Senyawa antioksidan yang teridentifikasi pada ekstrak minyak bekatul antara lain asam n-heksadekanoat, asam benzoat, dan asam klorogenat.

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Tocotrienols are members of the vitamin E family with neuroprotective, antioxidant, anticancer, and cholesterol-lowering properties. One source of tocotrienols is rice bran. Tocotrienols can be obtained from rice brain oil, which is one of the vegetable oils with the highest tocotrienol content. To enrich the levels of tocotrienols in rice brain oil, the rice bran will be fermented with the fungus Aspergillus terreus. This study observed the effect of variations in the solvent ratio of methanol:chloroform:water and fermentation by utilizing the fungus Aspergillus terreus during the process of extraction to increase the tocotrienol levels in rice bran oil. In this study, solid state fermentation will be carried out on the rice bran before the rice bran oil is extracted by using the Bligh-Dyer method and analyzed with UV spectrophotometer and GC/MS to determine the tocotrienol levels in rice bran oil. The results of this study showed how the optimum solvent ratio of methanol:chloroform:water to increase the extraction of tocotrienols was the ratio of methanol:chloroform:water 1:1:0,9 (v/v/v), with an increase in tocotrienol concentration from 2541,44 ppm to 3642,79 ppm, and how fermentation increased the tocotrienol levels in the extracted rice bran oil from 2541,44 ppm to 3257,66 ppm. The antioxidant compounds identified in rice bran oil extract include n-hexadecanoic acid, benzoic acid, and chlorogenic acid."

"Alpinetin merupakan senyawa bioaktif flavonoid yang diketahui memiliki berbagai macam manfaat, seperti antiinflamasi, antikanker, dan antioksidan dengan toksisitas sistemik yang rendah. Bekatul diketahui memiliki kandungan antioksidan (flavonoid). Bekatul adalah produk sampingan yang dihasilkan dari proses penggilingan padi. Pengayaan kandungan senyawa bioaktif dan asam lemak pada minyak bekatul dapat dilakukan dengan proses fermentasi menggunakan kapang Aspergillus terreus. Pada proses fermentasi dilakukan penambahan sumber karbon, yaitu glukosa untuk meningkatkan produktivitas asam lemak. Variasi konsentrasi glukosa dilakukan sebanyak lima variabel, yaitu 4, 6, 8, 10, dan 12 g/L. Minyak bekatul yang telah diekstraksi kemudian diuji menggunakan alat Liquid Cromatography Mass Spectrometry (LCMS) secara kualitatif. Dari penelitian ini didapatkan pada penambahan glukosa sebanyak 10 g/L dihasilkan yield lipid optimum sebesar 7,69% dan kandungan alpinetin tertinggi dihasilkan pada penambahan glukosa sebanyak 8g/L dengan persentase luas peak sebesar 27,11%.

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Alpinetin is a flavonoid bioactive compound that is known to have various benefits, such as anti-inflammatory, anticancer, and antioxidant with low systemic toxicity. Rice bran is known to contain antioxidants (flavonoids). Rice bran is a by-product of the rice milling process. Enrichment of the content of bioactive compounds and fatty acids in rice bran oil can be carried out by a fermentation process using Aspergillus terreus. In the fermentation process, a carbon source, namely glucose, is added to increase the productivity of fatty acids. Variations in glucose concentration were carried out by five variables: 4, 6, 8, 10, and 12 g/L. The extracted rice bran oil then tested using a Liquid Chromatography Mass Spectrometry (LCMS) qualitatively. From this research, it was found that the addition of 10 g/L glucose produced the optimum lipid yield 7,69% and the highest alpinetin content was produced with the addition of glucose as much as 8g/L with area percentage of 27,11%.

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"Penelitian ini bertujuan untuk mengetahui pertumbuhan Rhizopus azygosporus UICC 539 di medium Potato Sucrose Agar (PSA) pada suhu 51°C, 52°C, 53°C, 54°C, 55°C, mengetahui kemampuan R. azygosporus UICC 539 untuk memfermentasi campuran lumpur dan bungkil sawit (3:1) steril pada suhu 30C dan 40C dengan Solid-State Fermentation (SSF), dan analisis komposisi campuran lumpur dan bungkil sawit (3:1) steril setelah pertumbuhan R. azygosporus UICC 539. Persiapan inokulum dengan menumbuhkan kapang dalam Potato Sucrose Broth (PSB) secara fermentasi pada suhu 30C dan 40C selama 5 hari. Inokulum (10%, v/v) ditambahkan ke dalam campuran lumpur sawit dan bungkil sawit (3:1) dalam cawan Petri (diameter 9 cm) pada 30C dan 40C selama 5 hari. Analisis nutrien pada fermentasi campuran lumpur dan bungkil sawit berdasarkan Standar Nasional Indonesia (SNI-01-2891-1992). Parameter yang diuji yaitu, energi total, energi dari lemak, kadar air, kadar abu, lemak total, protein, dan karbohidrat total. Hasil penelitian menunjukkan R. azygosporus UICC 539 tidak tumbuh pada PSA di suhu 51, 52, 53, 54, 55C. Strain tersebut dapat memfermentasi campuran lumpur dan bungkil sawit (3:1) steril pada suhu 30°C dan 40°C dengan SSF. Pertumbuhan R. azygosporus UICC 539 pada campuran limbah menunjukkan peningkatan kadar air dan abu, penurunan kadar protein, total kalori dan kandungan karbohidrat. Tidak ada perubahan kalori dari lemak dan kadar lemak total dibandingkan dengan kontrol.

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This study aims to determine the growth temperature of Rhizopus azygosporus UICC 539 in Potato Sucrose Agar (PSA) at 51°C, 52°C, 53°C, 54°C, 55°C, to determine the ability of R. azygosporus UICC 539 to ferment mixture of slurry and palm kernel cake (3:1) sterile at 30°C and 40°C with Solid-State Fermentation (SSF), and analysis of the composition of a mixture of sterile slurry and palm kernel cake (3:1) after the growth of R. azygosporus UICC 539. Inoculum preparation by growing the mold in Potato Sucrose Broth (PSB) by fermentation at 30°C and 40°C for 5 days. Inocula (10%, v/v) were added to the mixture of slurry and palm kernel cake (3:1) in Petri dishes (9 cm diameter) at 30°C and 40°C for 5 days. Nutrient analysis in the mixed fermentation of slurry and palm kernel cake was carried out based on the Indonesian National Standard (SNI-01-2891-1992). The parameters tested were total energy, energy from fat, moisture content, ash content, total fat, protein, and total carbohydrates. The results showed that R. azygosporus UICC 539 did not grow on PSA at 51, 52, 53, 54, 55C. The strain could ferment a mixture of slurry and palm kernel cake (3:1) sterile at 30°C and 40°C with SSF. The growth of R. azygosporus UICC 539 in the waste mixture showed an increase in water and ash content, a decrease in protein content, total calories and carbohydrate content. There were no changes in calories from fat and total fat content compared to controls."

"Beras merah (Oryza sativa L. var. Inpari 24) mengandung polifenol dan oryzanol yang bermanfaat sebagai anti-aging. Fermentasi dapat meningkatkan kandungan fenolik dan flavonoid sehingga fermentasi air rendaman beras merah berpotensi meningkatkan aktivitas antielastase untuk pencegahan penuaan kulit. Mikroorganisme seperti bakteri pada hasil fermentasi dapat dikembangkan menjadi produk perawatan kulit karena diketahui dapat menangkal sinar ultraviolet. Penelitian ini bertujuan mengetahui perbandingan aktivitas antielastase pada air rendaman beras merah yang difermentasi secara spontan (FS), dengan ragi tapai (FR), dan tidak difermentasi (NF). Selain itu, untuk mengetahui bakteri apa yang dapat dipertimbangkan sebagai bahan dasar produk skincare. Metode ekstraksi dilakukan dengan perebusan beras merah dan UAE, fermentasi dilakukan secara spontan dan dengan penambahan ragi tapai. Identifikasi bakteri dilakukan dengan metode PCR. Setiap sampel ditetapkan kadar fenol dan flavonoid total, serta diuji aktivitas antielastasenya dengan mengukur absorbansi sampel. Hasil pengukuran persentase inhibisi enzim elastase sampel FS, FR, dan NF berturut-turut sebesar 66,20% (meningkat 18,36% dibanding NF); 71,79% (meningkat 28,35% dibanding NF); dan 55,93% dengan konsentrasi 150.000 ppm. Dari sampel FS dan FR dilakukan isolasi bakteri dan didapatkan lima isolat dari sampel FS dan dua isolat dari sampel FR. Hasil isolasi bakteri kemudian dilakukan PCR, dianalisis sekuensing, dan dianalisis dengan pohon filogenetik. Berdasarkan analisis filogenetik, isolat FS berkerabat dekat dengan Enterobacter sp., Pantoea agglomerans, Enterobacter mori dan Enterobacter hormaechei. Sementara itu, isolat FR berkerabat dekat dengan Enterobacter cloacae dan Enterobacter mori. Hasil penelitian ini menunjukkan bahwa fermentasi dapat meningkatkan aktivitas penghambatan terhadap enzim elastase secara signifikan yang mungkin terjadi akibat adanya Enterobacter dan Pantoea agglomerans selama fermentasi.

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Red rice (Oryza sativa L. var. Inpari 24) contains polyphenolic compounds and oryzanol, which have anti-aging properties. Fermentation can increase phenolic and flavonoid content, thus fermentation of red rice water has the potential to enhance antielastase activity for skin aging prevention. Microorganisms such as bacteria in the fermentation product can be develop into skincare products due to their known ability to counteract ultraviolet rays. Therefore, this study aims to compare the antielastase activity of spontaneously fermented red rice water (FS), fermented with tapai yeast (FR), and unfermented (NF). Additionally, it aims to identify bacteria that could be considered as a base for skincare products. The extraction method involved boiling red rice and UAE, fermentation was carried out spontaneously and with the addition of tapai yeast. Bacterial identification was done using the PCR method. Each sample was then determined for total phenol and flavonoid content and tested for antielastase activity by measuring sample absorbance. The inhibition percentages of elastase enzyme for FS, FR, and NF samples were 66.20% (increased by 18,36% compared to NF); 71.79% (increased by 28,35% compared to NF); and 55.93% respectively, at a concentration of 150,000 ppm. From the FS and FR samples, bacterial isolation was conducted, yielding five isolates from the FS sample and two isolates from the FR sample. The bacterial isolates were then subjected to PCR, sequenced, and analyzed phylogenetically. Based on the phylogenetic analysis, FS isolates were kin to Enterobacter sp., Pantoea agglomerans, Enterobacter mori, and Enterobacter hormaechei. Meanwhile, FR isolates were kin to Enterobacter cloacae and Enterobacter mori. This study indicate that fermentation can significantly enhance elastase enzyme inhibition, possibly due to the presence of Enterobacter and Pantoea agglomerans during fermentation."