Claim Missing Document
Check
Articles

Found 27 Documents
Search

KINETIKA REAKSI ENZIMATIS EKSTRAK KASAR ENZIM SELULASE BAKTERI SELULOLITIK HASIL ISOLASI DARI BEKATUL Saropah, Dyah Ayu; Jannah, Akyunul; Maunatin, Anik
ALCHEMY ALCHEMY (Vol.2 No.1
Publisher : Department of Chemistry, Faculty of Science and Technology UIN Maulana Malik Ibrahim Malan

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (350.138 KB) | DOI: 10.18860/al.v0i0.2297

Abstract

Bran rice is a by-product of rice into rice milling process, the cellulose content of 40-60%, so the potential as a carbon source for the growth of microorganisms such as bacteria to produce enzymes particularly cellulolytic bacteria. The purpose of the study was to determine the diversity of the characters from the cellulolytic bacterial isolates and optimum conditions enzyme (cellulase enzymes rough) so that they can hydrolyze the cellulose to glucose with either rice bran. The characterization includes the determination of pH, temperature and time of optimum crude extract of bacterial cellulolytic enzyme cellulase, determination of Vmax and Km and molecular mass determination of cellulase.Research methods include making media, regeneration of isolates, bacterial growth curve manufacturing, production of cellulase enzymes from bacterial cellulolytic rough at the optimum conditions, the kinetics of enzymatic reaction: substrate concentration factor of the reaction rate (with variation of the concentration of 0.50%, 0.75%, 1 , 00%, 1.25% and 1.50% (w / v)) followed by calculating the Vmax and Km.The results showed that the enzyme cellulase of cellulolytic bacteria isolated from rice bran result that has optimum conditions at pH 7.5, temperature 50 ° C, 40 min incubation time to produce Vmax 0.0086 units / mL and Km 1.694%.
Isolation and Characterization of Rice Bran Protein Using NaOH Solution Jannah, Akyunul
ALCHEMY ALCHEMY (Vol.4, No.1
Publisher : Department of Chemistry, Faculty of Science and Technology UIN Maulana Malik Ibrahim Malan

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (249.156 KB) | DOI: 10.18860/al.v4i1.3160

Abstract

The high protein content in rice bran potential to be developed into food. The purpose of this study was to isolate the protein in rice bran using NaOH solution with various concentration of 0.05; 0.1; 0.15; 0.2 M and characterization of functional properties. The results showed the concentration of 0.2 M NaOH produced the best results. The protein content obtained was 82%, stability of  emulsion of 42% and 47% stabilty of foam. Keywords: NaOH, protein, rice bran
UJI AKTIVITAS ANTIBAKTERI SENYAWA KATEKIN DARI DAUN TEH (Cameliasinensis L.var assamica) TERHADAP BAKTERI Micrococcusluteus Rustanti, Elly; Jannah, Akyunul; Fasya, Ahmad Ghanaim
ALCHEMY ALCHEMY (Vol.2 No.2
Publisher : Department of Chemistry, Faculty of Science and Technology UIN Maulana Malik Ibrahim Malan

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (87.621 KB) | DOI: 10.18860/al.v0i0.2886

Abstract

Zat antibakteri merupakan suatu zat yang dapat mengganggu pertumbuhan dan metabolisme bakteri, sehingga zat tersebut dapat menghambat pertumbuhanatau bahkan membunuh bakteri. Penelitian ini bertujuan untuk memanfaatkan bahan alam sebagai antibakteri alami. Penelitian ini ingin mengetahui bahwa daun teh (Camellia sinensis L. var assamica) yang efektif sebagai antibakteri alami dapat menghambat bakteri Micrococcus luteus. Penelitian ini meliputi ekstraksi yang dilakukan dengan metode maserasi menggunakansampel daun teh. Pemisahan ekstrak katekin dilakukan dengan KLT Analitik dengan variasi eluen yaitu etil asetat:air:asam format (18:1:1), toluena:aseton:asam format (3:3:1) dan kloroform:metanol:air (6,5:3,5:1), untuk mencari eluen terbaik yang selanjutnya digunakan untuk KLT Preparatif. Selanjutnya hasil dari KLT Preparatif digunakan untuk uji antibakteri.Hasil penelitian  menunjukkan bahwa  hasil ekstrak katekin dari daun teh ± 3,34 gram dari 50 gram sampel. Hasil KLT Analitik menunjukkan bahwa eluen terbaik untuk KLT Preparatif adalah etil asetat:air: asam format. Hasil uji antibakteri menunjukkan bahwa isolat 5 dari ekstrak daun teh memberikan efektivitas terbaik sebagai antibakteri Micrococcus luteus.
ISOLASI DAN KARAKTERISASI GELATIN DARI TULANG AYAM DENGAN METODE ASAM Jannah, Akyunul; Maunatin, Anik; Windayanti, Arin; Findianti, Yuana; Mufidah, Zulfiatul
ALCHEMY ALCHEMY (Vol.2, No.3
Publisher : Department of Chemistry, Faculty of Science and Technology UIN Maulana Malik Ibrahim Malan

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (167.181 KB) | DOI: 10.18860/al.v0i0.2904

Abstract

The purpose of this study was to determine the quality of gelatin by using raw materials bone chicken (Gallus gallus domesticus) and the Broiler chickens for differences in the concentration of acetic acid immersion process ( curing ).The method used in this study is the preparation and broiler chicken bones , isolation of gelatin with various concentration of acetic acid in the curing process , the process of hydrolysis , extraction temperature rise and gelatin with gelatin obtained include the characterization of protein , water , ash and metal.The results showed the highest yield of gelatin produced from Broiler chicken bone types with acetic acid concentration of 1 % , ie 3.25%. Gelatin highest protein content of 86.27 % of the types of Broiler chicken bone with acetic acid concentration of 1.5 %. Lowest ash content of 15.7 % gelatin from bone types Broiler chicken with 1 % acetic acid concentration , and from analysis using AAS contained Cu at 0.6 % (of the type of chicken bones, acetic acid concentration of 0.5 %) and Cu metal content of 1.1 % (of the type of Broiler chicken bones, acetic acid concentration of 1 %. highest moisture content of 0.17 % gelatin from bone types Kampung chicken with 1 % acetic acid concentration
HIDROLISIS GUGUS METOKSIL PEKTIN AMPAS TEBU UNTUK MENGHASILKAN BIOMETANOL Akyunul Jannah; Arief Suryadinata
SAINSTIS SAINSTIS (Vol 1, No 2
Publisher : Lembaga Penelitian dan Pengembangan Universitas Islam Negeri Maulana Malik Ibrahim Malang.

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (711.294 KB) | DOI: 10.18860/sains.v0i0.2303

Abstract

Methanol is a potential in two areas, namely as fuel cells and biodiesel. Among the many biomass, pectin is one of the best for the production of methanol. The purpose of this study was to determine the influence of pectin methyl esterase enzyme  concentration  (PME)  group  metoksil  rough  on  pectin  hydrolysis  of bagasse to produce the highest levels of biometanol. Methods This study includes the preparation of the bagasse, further hydrolysis using crude extract of the enzyme pectin methyl esterase (PMEs) resulting from bacterial culture Bacillus subtilis at Borth Nutrient media (NB) with 1% pectin. Hydrolysis of Metoksil groups of poligalakturonat acid in the pectin bagasse to obtain the concentration of methanol to vary the enzyme crude extract PMEs. Concentration of crude enzyme extract PMEs used was 10%, 15%, 20% and 25% in 24-hour incubation with 2 repetitions performed. The resulting methanol levels were analyzed using GC (Gas Chromatography). The results of this study concluded that allowing the concentration used for hydrolysis of bagasse to produce methanol using crude enzyme from  Bacillus subtilis (PMEs) is 10% with a methanol content of 0.02%.
Synthesis Of L-Menthyl Acetic by Esterification L-Menthol and Acetic Anhydride with Variation Of Time Novia Suryani; A Ghanaim Fasya; Rurini Retnowati; Akyunul Jannah
Al-Kimia Vol 8 No 1 (2020): JUNE
Publisher : Study Program of Chemistry - Alauddin State Islamic University of Makassar

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (693.862 KB) | DOI: 10.24252/al-kimia.v8i1.11965

Abstract

l-menthyl acetic is an ester with specific aroma that synthesized by reaction of l-menthol and acetic anhydride and useful in fragrance industry. This paper reports influenced variation of time reaction toward ester product and characteristics l- menthyl acetic based on TLC, FTIR, GC and GC-MS. Reaction using l-menthol, acetic anhydride and catalyst H­2­SO­4­ 98 % in diethyl eter solvent at temperature 60 °C with variation of time reaction (45, 60, 75, 90, 105 minutes). The result of research is variation of time influence product with highest yield 88,43 % for 90 minutes. Monitoring TLC achived R­f­ = 0,82; analysis by FTIR achived specific wave number ester 1736,96 cm-1; analysis by GC achived t­r­ = 14,82 minutes and analysis by GC-MS achived t­r­ = 16,13 minutes with base peak m/z = 95.
IDENTIFIKASI SENYAWA DAN AKTIVITAS ANTIMALARIA IN VIVO EKSTRAK ETIL ASETAT TANAMAN ANTING-ANTING (Acalypha indica L.) Elok Kamilah Hayati; Akyunul Jannah; Rachmawati Ningsih
Molekul Vol 7, No 1 (2012)
Publisher : Universitas Jenderal Soedirman

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (428.59 KB) | DOI: 10.20884/1.jm.2012.7.1.103

Abstract

Telah dilakukan penelitian identifikasi ekstrak etil asetat dari tanama Anting-anting (Acalypha indica Linn.) sebagai senyawa antimalaria dan aktivitasnya secara in vivo pada sel parasit malaria P. berghei.Penelitian ini meliputi ekstraksi tanaman anting-anting menggunakan metode ekstraksi maserasi selama 24 jam dengan variasi pelarut yaitu etil asetat, diklorometana, dan petroleum eter. Pengadukkan dibantu dengan shaker selama 3 jam. Ekstrak pekat diuji fitokimia didukung Kromatografi Lapis Tipis, Ekstrak pekat etil asetat dilakukan uji antimalaria in vivo terhadap hewan uji terhadap sel parasit P. berghei. Data derajat parasitemia mencit dianalisis menggunakan program SPSS dengan Uji OneWay ANOVA dan dilanjutkan dengan Uji Tukey.Hasil penelitian menunjukkan adanya senyawa aktif tanin, alkaloid dan steroid pada ekstrak etil asetat.Uji aktivitas antimalaria secara in vivo pada hewan coba didapatkan hasil penghambatan ekstrak etilasetat terhadap pertumbuhan Plasmodium berghei pada dosis 0,01 mg/g bb sebesar 87,19%; pada dosis 0,1mg/g bb sebesar 84,9% dan pada dosis 1mg/g bb sebesar 90,74%.
Isolation, Cellulase Activity Test and Molecular Identification of Selected Cellulolytic Bacteria Indigenous Rice Bran Akyunul Jannah; Aulanni`am Aulanni`am; Tri Ardyati; Suharjono Suharjono
Indonesian Journal of Chemistry Vol 18, No 3 (2018)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (357.537 KB) | DOI: 10.22146/ijc.26783

Abstract

Rice bran is the waste product of rice milling which is abundant in Indonesia, it can be used as a raw material for the manufacture of bioethanol by fermentation. Before being fermented, rice bran must be hydrolyzed into glucose by biomass degrading. This study was aimed to isolate indigenous cellulolytic bacteria from rice bran as producer of cellulolytic enzymes and resulted in 22 bacterial isolates that demonstrated cellulolytic activity being identified. Among them, BE 8 and BE 14 isolates showed the highest endoglucanase activity at 2.16 and 1.31 U/mL respectively. Identification of the 16S rDNA showed that BE 8 belongs to Bacillus subtilis and BE 14 in Bacillus cereus.
Optimization Chicken Bones Gelatin Extraction Using Hydrochloric Acid Immersion and Multi-Stage Thermal Treatment Deva Krisna Kadarani; Akyunul Jannah
ALCHEMY:Journal of Chemistry Vol 10, No 1 (2022): ALCHEMY: Journal of Chemistry
Publisher : Department of Chemistry, Faculty of Science and Technology UIN Maulana Malik Ibrahim Malan

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.18860/al.v10i1.13372

Abstract

The growing poultry consumption rate yearly includes chicken with significantly increased amounts of by-products like skin and bones. Chicken bones are unused properly even if the bone is rich in collagen which is the primary material to produce gelatin. Gelatin usually is generated by bovine and porcine, but some health and religious issues have successfully forbid using both resources. Chicken bones could be an alternative material for gelatin production. This research aimed to investigate chicken bones as a substitute resource for gelatin manufacturing using hydrochloric acid submersion in collaboration with multi-stage thermal treatment. Chicken bones were proceeded in several steps such as degreasing, decontamination, resizing, demineralization using a hydrochloric acid immersion (1.50, 3.00, 4.50, and 6.00% v/v) for 24 and 48 hours, addition gelatin extraction using multi-stages thermal process (55, 65, and 75°C) for 4 hours each temperature subsequentially, evaporating, drying, and shaping a gelatin powder. This study produced type A gelatin which investigated yield number, moisture and ash content, gel strength, acidity level, and functional group using Fourier-transform Infrared (FTIR) spectroscopy. The sample gelatin has obtained at least 2% up to 8% yields. The moisture and ash contents were suitable to the commercial specification range, 4-12%, and 0.1-0.4%, respectively. The acid conditioning process has an impact on acidity with pH levels 4.40-5.44. Based on gelatin standards, this study declared that processing chicken bones using 6.00% hydrochloric acid submersion for 24 hours was optimal for gelatin extraction. Those optimal condition has formed gelatin with more than 8% yields. It was considered great gelatin with 260.57 g Bloom of gel strength and 90.18% of emulsion stability. Sample gelatin has a quite reasonable acidity level at 4.5. Protein structures confirmation using the vibration of the best gelatin sample has also shown essential components such as O-H, N-H, and C=O on the FTIR spectrum.Keywords: chicken bones (Gallus domesticus), hydrochloric acid immersion, gel strength, emulsion stability, FTIR spectroscopy
Identifikasi dan Uji Toksisitas terhadap Larva Udang (Artemia salina L.) Ekstrak Bekatul Menggunakan Variasi Jenis Pelarut dan Lama Ekstraksi Dewi Wardatul Jannah; Anik Maunatin; Akyunul Jannah
ALCHEMY:Journal of Chemistry Vol 8, No 2 (2020): ALCHEMY: Journal of Chemistry
Publisher : Department of Chemistry, Faculty of Science and Technology UIN Maulana Malik Ibrahim Malan

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.18860/al.v8i2.11512

Abstract

 Rice bran was extracted using ultrasonic method with varied solvents (ethanol, ethyl acetate and n-hexane) and extraction times (20, 25 and 30 minutes). The aim of this study was to determine toxicity value of rice bran extract with variation of solvents and extraction times. Rice bran extracts were tested its toxicity by BSLT method and its secondary metabolite by phytochemical test with reagents. Mortality data of shrimp larvae was analyzed by probit to determine LC50 values. Yield of ethanolic extract of rice bran for E1-20, E1-25 and E1-30 samples was 18.159, 19.132 and 18.280%, respectively. Rice bran extracts by ethyl acetate solvent (E2) and n-hexane (E3) gave different yields such as 8.302% (E2-20), 7.282% (E2-25), 9.18% (E2-30), 7.815% (E3-20), 7.125% (E3-25), and 7.279% (E3-30). All of rice bran extracts contained flavonoids, steroids and triterpenoids. LC50 values in ethanolic extract of rice bran for E1-20, E1-25 dan E1-30 samples were 613.258, 673.210 and 2217.255 ppm, respectively. Toxicity (LC50) values of ethyl acetate extract of rice bran were 1161.298 ppm (E2-20), 1170.774 ppm (E2-25) and 701.532 ppm (E2-30), while toxicity (LC50) values of n-hexane extract of rice bran were 592.901 ppm (E3-20), 617.425 ppm (E3-25) and 695.198 ppm (E3-30). Keywords: Rice bran, secondary metabolite, toxicity, ultrasonic method  Bekatul diekstrak menggunakan metode ultrasonik dengan variasi pelarut (etanol, etil asetat dan n-heksana) dan lama ekstraksi (20, 25 dan 30 menit). Tujuan penelitian ini adalah mengetahui nilai toksisitas ekstrak bekatul dengan variasi pelarut dan lama ekstraksi. Ekstrak bekatul diuji kemampuan toksisitas terhadap larva udang dengan metode BSLT dan diuji fitokimia dengan reagen. Data kematian larva udang dianalisis dengan analisis probit untuk menentukan nilai LC50. Rendemen ekstrak etanol bekatul yang diperoleh pada sampel E1-20, E1-25 dan E1-30 masing-masing sebesar 18,159; 19,132; dan 18,280%. Adapun rendemen ekstrak etil asetat dan n-heksana bekatul sebesar 8,302% (E2-20), 7,282% (E2-25), 9,18% (E2-30), 7,815% (E3-20), 7,125% (E3-25) dan 7,279% (E3-30). Senyawa metabolit sekunder yang terkandung pada masing-masing ekstrak adalah flavonoid, steroid dan triterpenoid. Nilai LC50 ekstrak etanol pada masing-masing sampel E1-20, E1-25 dan E1-30 adalah 613,258; 673,210 dan 2217,255 ppm. Ekstrak etil asetat bekatul pada sampel E2-20, E2-25 dan E2-30 memberikan nilai toksisitas dengan LC50 sebesar 1161,398; 1170,774 dan 701,532 ppm, berturut-turut. Nilai toksisitas (LC50) ekstrak n-heksana pada sampel E3-20, E3-25 dan E3-30 adalah 592,901; 617,425 dan 695,198 ppm, berturut-turut. Kata kunci: Bekatul, metabolit sekunder, toksisitas, metode ultrasonik