Objective: This study aimed to increase the yield of microcrystalline cellulose (MCC) made from water hyacinth ɑ-cellulose by enzymatic hydrolysis by using purified enzyme and to find it’s characteristics compared to the reference. Methods: In this research, MCC was prepared from water hyacinth powder through the chemical isolation process of ɑ-cellulose, followed by enzymatic hydrolysis with purified cellulase from Chaetomium globosum. The yield of MCC was improved by using purified enzyme and optimization of temperature, pH, and hydrolysis time. Identification was carried out by using ZnCl and infrared spectrophotometry, followed by characterization of MCC include particle size analysis (PSA) and diffractogram pattern (X-Ray Diffraction) compared to reference Avicel PH 101. Results: Purified enzyme from Chaetomium globosum has high activity with a clear zone area of 45 mm with cellulolytic index 6.5 that almost same as Trichoderma reesei (50 mm), with the cellulase enzyme activity of 6.691 U/ml. The optimum condition was at a temperature of 50⁰C and pH 6.0 with the hydrolysis time of 2 h, which produced 95% yield of MCC. Identification with ZnCl and FTIR spectrum showed positive results, similar to the reference. The results of organoleptic test, particle size analysis, and diffractogram pattern (X-Ray Diffraction) showed crystalline characteristic similar to reference (Avicel PH 101). Conclusion: Enzyme from Chaetomium globosum has a higher activity of cellulase than Trichoderma reesei with MCC obtained was 95%. Based on the comparison of the organoleptic test, particle size analysis, and diffractogram pattern, MCC from water hyacinth has a great potential which showed similar characteristic to reference (Avicel pH 101).
Objective: This study aimed to increase the yield of microcrystalline cellulose (MCC) from kapok pericarpium alpha-cellulose produced by enzymatic hydrolysis using purified cellulase from Termites (Macrotermes gilvus) and to compare the characteristics with the reference product. Methods:In this research, MCC was prepared from kapok pericarpium powder through the chemical isolation process of alpha-cellulose, followed by enzymatic hydrolysis with purified cellulase from Macrotermes gilvus. The yield was improved by using purified cellulase in optimized temperature, pH, and hydrolysis time. Identification was carried out by using ZnCl and infrared spectrophotometry, followed by characterization of MCC include particle size analysis (PSA) and diffractogram pattern (X-Ray Diffraction). The results were compared with Avicel PH 101 as the reference product. Results:Purified cellulase from Macrotermes gilvus showed high cellulose activity. Cellulose in the concentration of 11.743 U/ml formed 49 mm clear zone area with cellulolytic index 7.16 that similar to the formed clear zone area of Trichoderma reesei (50 mm), the optimum hydrolysis condition was achieved at 50 °C, pH 6.0, in 2 h, which produced 80% yield of MCC. Produced MCC was analyzed with ZnCl and FTIR spectrum resulting in positive results, similar to reference. The results of the organoleptic test, particle size analysis, and diffractogram pattern (X-Ray Diffraction) showed crystalline characteristics of MCC is similar to the reference (Avicel PH 101). Conclusion:Cellulase Macrotermes gilvus yielded 80% MCC and higher enzymatic activity than Trichoderma reesei. Based on the organoleptic test, particle size analysis, and diffractogram pattern observation, MCC from kapok pericarpium has shown similar characteristics to reference (Avicel pH 101) and might be potential to be further developed.
Abstrak: Indonesia memiliki banyak tanaman obat-obatan yang bisa digunakan untuk mengobati berbagai penyakit. Salah satu tumbuhan yang digunakan sebagai obat adalah daun karamunting (Rhodomyrtus tomentosa (Aiton)Hassk.). Secara tradisional daun Karamuting digunakan di masyarakat untuk mengobati karies gigi, mengobati luka dan kudis. Penelitian ini bertujuan untuk mengetahui pengaruh efek antibakteri ekstrak etanol daun karamunting terhadap bakteri Streptococcus mutans dengan menggunakan metode sumuran. Penelitian ini menggunakan penelitian eksperimental laboratorium. Sampel penelitian adalah ekstrak etanol daun karamunting. Ekstrak diuji aktivitas antibakteri terhadap Streptococcus mutans menggunakan metode difusi sumuran dengan konsentrasi 6,25%; 12,5%; 25%; 50% b/v. Hasil penelitian menunjukkan ekstrak Etanol daun karamunting mempunyai aktivitas antibakteri terhadap Streptococcus mutans pada konsentrasi 6,25%; 12,5%; 25%; 50% b/v masing-masing dengan diameter zona hambat sebesar 17,7±0,0577, 22,6±0,2516, 25,3±0,1527, and 28,3±0,0577. Ekstrak etanol daun karamunting mempunyai daya antibakteri terhadap Streptococcus mutans yang terbesar terdapat pada konsentrasi 50% dengan diameter 28,3 mm.
This study aims to obtain cellulase enzymes from selected molds for microcrystalline cellulose preparation from ????-cellulose of kapok cortex. Alpha-cellulose was obtained by biodelignification, and the purified cellulase was obtained from the selected mold. The Microcrystalline cellulose obtained from enzymatic hydrolysis was then identified FTIR and DSC, followed by characterization of microcrystalline cellulose, Particle Size and Distribution Analysis (PSA), and Scanning Electron Microscope-Energy Dispersive X-ray (SEM-EDX), Loss on drying, pH, bulk density, tapped density, and flow rate. Biodelignification produced 14.88% ????-cellulose, Penicillium sp. the selected mold had the highest cellulase activity, with a cellulolytic index of 4.83. FTIR identification was similar to Avicel PH 101 with a melting point of 244.580°C. Loss on drying was 3.74%, pH was 7.0, particle size ranged from 13.06 to 196.79 ????m, bulk density and tapped density were 0.11 g/cm3 and 0.23 g/cm3, respectively flow rate character is quite good. SEM-EDX was showed that the morphological shape of the microcrystalline cellulose of the kapok cortex is elongated. Microcrystalline cellulose has shown a quite similar in character and can be furthered.
Objective: This study aimed to find psychochemical properties of microcrystalline cellulose (MCC) obtained from α-cellulose kapok pericarpium. Methods: The cellulase activity was screened by clear zone and sugar reduction method. The enzym from selected mold was purified by diethylaminoethyl (DEAE) chromatography. α-cellulose of kapok pericarpium was hydrolyzed using the purified cellulase enzymes. Microcrystalline cellulose (MCC) identified by Fourier transform infrared (FTIR) spectrometry, and qualitative analysis test. The samples were characterized for pH test, x-ray diffraction (XRD), and particle size analyzer (PSA). Results: The optimum cellulase activity was shown by Penicillium vermiculatum. It’s clear zone diameter around 3 cm and the cellulase activity was 67.73±0.25 mU/ml. The strongest cellulase activity was detected from 1st fraction (P1) out of 6 column fractions with optimum activity at 1.177±2 mU/ml. The optimal conditions for microcrystalline cellulose (MCC) preparation were at 50 ˚C, for 2 ours, using 20 ml of acetate buffer pH 5 and 2 ml of cellulase enzyme. Microcrystalline cellulose (MCC) obtained at 78% w/w and its FTIR spectrum and x-ray diffractogram similar to reference while the pH of MCC was fulfilled requirements of The United States Pharmacopoeia 2007. Conclusion: The use of purified enzyme of cellulase has succeded in microcrystalline cellulose (MCC) preparation andmicrocrystalline cellulose (MCC) obtained was 78% w/w, with similar characteristics to reference (Avicel PH 101) and the pH of MCC was fulfilled requirements of The United States Pharmacopoeia 2007.
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