Muhammad Akbar S Kurniawan, Muhamad Jalil Baari, Sariyanti Sariyanti, Finarisnawati Finarisnawati
Malaria is a serious caused by protozoan parasites such as Plasmodium groups and has fatal consequences for human health. The increase in the resistance of the Plasmodium parasites toward existing antimalarial drugs prompts the exploration of novel compounds. In this study, quantitative structure-activity relationship (QSAR) analysis using the semi-empirical AM1 method was conducted to identify the optimal model that relates physicochemical properties and biological activity of chalcone derivatives. In addition, ADMET prediction and molecular docking were also carried out. Multilinear regression calculations for statistical parameters of QSAR models revealed that Model 4, with 11 independent variables, provided the best predictions and exhibited a robust correlation with antimalarial activity represented by inhibitory concentration (IC50). ADMET predictions indicated favorable absorption, distribution, metabolism, excretion, and toxicity properties, particularly for B2D, showing promising antimalarial attributes. Molecular docking studies targeting 5 mutated PfDHODH proteins revealed B2D’s potential to reach therapeutic targets efficiently. It has low docking scores for mutations I (-10.5 kcal/mol), II (-8.6 kcal/mol), and V (-10.5 kcal/mol) with RMSD < 2Å, in carrying out its role for antimalarial activity. This research successfully identifies B2D as an efficient inhibitor of PfDHODH receptors. Thus, it is a highly promising novel antimalarial drug.
{"title":"QSAR ANALYSIS USING SEMI-EMPIRICAL AM1 METHOD, MOLECULAR DOCKING, AND ADMET STUDIES OF CHALCONE DERIVATIVES AS ANTIMALARIAL COMPOUNDS","authors":"Muhammad Akbar S Kurniawan, Muhamad Jalil Baari, Sariyanti Sariyanti, Finarisnawati Finarisnawati","doi":"10.20473/jkr.v8i2.51798","DOIUrl":"https://doi.org/10.20473/jkr.v8i2.51798","url":null,"abstract":"Malaria is a serious caused by protozoan parasites such as Plasmodium groups and has fatal consequences for human health. The increase in the resistance of the Plasmodium parasites toward existing antimalarial drugs prompts the exploration of novel compounds. In this study, quantitative structure-activity relationship (QSAR) analysis using the semi-empirical AM1 method was conducted to identify the optimal model that relates physicochemical properties and biological activity of chalcone derivatives. In addition, ADMET prediction and molecular docking were also carried out. Multilinear regression calculations for statistical parameters of QSAR models revealed that Model 4, with 11 independent variables, provided the best predictions and exhibited a robust correlation with antimalarial activity represented by inhibitory concentration (IC50). ADMET predictions indicated favorable absorption, distribution, metabolism, excretion, and toxicity properties, particularly for B2D, showing promising antimalarial attributes. Molecular docking studies targeting 5 mutated PfDHODH proteins revealed B2D’s potential to reach therapeutic targets efficiently. It has low docking scores for mutations I (-10.5 kcal/mol), II (-8.6 kcal/mol), and V (-10.5 kcal/mol) with RMSD < 2Å, in carrying out its role for antimalarial activity. This research successfully identifies B2D as an efficient inhibitor of PfDHODH receptors. Thus, it is a highly promising novel antimalarial drug.","PeriodicalId":502957,"journal":{"name":"Jurnal Kimia Riset","volume":"41 10","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139184839","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nazaratun Thaiyibah, Mochammad Yuwono, Ahmad Yudianto
Identifying the concentration of alcohol compounds in postmortem analysis of biological fluids can help the investigation, just as postmortem analysis of gastric juices can reveal the concentrations of alcohol consumed. However, an efficient and effective combination of extraction and measurement methods is required when looking at complex postmortem samples. Therefore, a headspace-solid phase microextraction (HS-SPME) method was developed using gas chromatography with a flame ionization detector (GC-FID) to identify postmortem alcohol concentrations. This present study optimizes and validates an effective and efficient method for postmortem alcohol extraction and quantification in gastric fluid. The optimal conditions for HS-SPME extraction using 65μm Polydimethy lsiloxane Divinyl benzene (PDMS/DVB) fiber for analyte isolation were 15 minutes. at 60°C and an exposure time of 1 minute. The validation investigation shows that the suggested approach satisfies the criteria for linearity, precision, accuracy, LOD, and LOQ for postmortem measurement of alcohol in gastric fluid.
{"title":"VALIDATION OF HEADSPACE SOLID-PHASE MICROEXTRACTION WITH GAS CHROMATOGRAPHY-FLAME IONISATION DETECTOR METHOD FOR ALCOHOL ANALYSIS ON GASTRIC FLUID","authors":"Nazaratun Thaiyibah, Mochammad Yuwono, Ahmad Yudianto","doi":"10.20473/jkr.v8i2.44502","DOIUrl":"https://doi.org/10.20473/jkr.v8i2.44502","url":null,"abstract":"Identifying the concentration of alcohol compounds in postmortem analysis of biological fluids can help the investigation, just as postmortem analysis of gastric juices can reveal the concentrations of alcohol consumed. However, an efficient and effective combination of extraction and measurement methods is required when looking at complex postmortem samples. Therefore, a headspace-solid phase microextraction (HS-SPME) method was developed using gas chromatography with a flame ionization detector (GC-FID) to identify postmortem alcohol concentrations. This present study optimizes and validates an effective and efficient method for postmortem alcohol extraction and quantification in gastric fluid. The optimal conditions for HS-SPME extraction using 65μm Polydimethy lsiloxane Divinyl benzene (PDMS/DVB) fiber for analyte isolation were 15 minutes. at 60°C and an exposure time of 1 minute. The validation investigation shows that the suggested approach satisfies the criteria for linearity, precision, accuracy, LOD, and LOQ for postmortem measurement of alcohol in gastric fluid.","PeriodicalId":502957,"journal":{"name":"Jurnal Kimia Riset","volume":"40 12","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139184843","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Multicomponent reactions involving three or more reactants are commonly used to prepare dihydropyrimidinone with various bioactivities. This study reports the different routes for the synthesis of benzaldehyde-based dihydropyrimidinone via the Biginelli reaction and investigates the yield of the obtained products. The synthesis was performed via routes A, B, C, D, and E based on the formation of iminium, enamine, and Knoevenagel intermediates between urea, benzaldehyde, and ethyl acetoacetate. Route A, through a one-pot reaction via iminium, produced dihydropyrimidinone with a yield of 58%. The product from route B via iminium was obtained in 62% yield. Route C and D occurred via enamine at room temperature, and reflux gave the product 31% and 40% yield, respectively. Route E involving Knoevenagel intermediate provided the product in a 38% yield. 1H NMR, FTIR, and MS spectroscopic techniques were used for structure elucidation.
涉及三个或更多反应物的多组分反应常用于制备具有各种生物活性的二氢嘧啶酮。本研究报告了通过 Biginelli 反应合成苯甲醛基二氢嘧啶酮的不同路线，并考察了所获产物的收率。根据脲、苯甲醛和乙酰乙酸乙酯之间形成的亚氨基、烯胺和 Knoevenagel 中间体，通过路线 A、B、C、D 和 E 进行了合成。路线 A 通过亚氨基的一锅反应生成了二氢嘧啶酮，产率为 58%。路线 B 通过亚氨基反应得到的产物收率为 62%。路线 C 和 D 在室温下通过烯胺进行反应，回流后得到的产物收率分别为 31% 和 40%。路线 E 涉及 Knoevenagel 中间体，产物的收率为 38%。1H NMR、傅立叶变换红外光谱和 MS 光谱技术被用于阐明结构。
{"title":"DIFFERENT ROUTES FOR THE SYNTHESIS OF BENZALDEHYDE-BASED DIHYDROPYIMIDINONES VIA BIGINELLI REACTION","authors":"Yan Alamanda Ilfahmi, Arif Fadlan","doi":"10.20473/jkr.v8i2.45209","DOIUrl":"https://doi.org/10.20473/jkr.v8i2.45209","url":null,"abstract":"Multicomponent reactions involving three or more reactants are commonly used to prepare dihydropyrimidinone with various bioactivities. This study reports the different routes for the synthesis of benzaldehyde-based dihydropyrimidinone via the Biginelli reaction and investigates the yield of the obtained products. The synthesis was performed via routes A, B, C, D, and E based on the formation of iminium, enamine, and Knoevenagel intermediates between urea, benzaldehyde, and ethyl acetoacetate. Route A, through a one-pot reaction via iminium, produced dihydropyrimidinone with a yield of 58%. The product from route B via iminium was obtained in 62% yield. Route C and D occurred via enamine at room temperature, and reflux gave the product 31% and 40% yield, respectively. Route E involving Knoevenagel intermediate provided the product in a 38% yield. 1H NMR, FTIR, and MS spectroscopic techniques were used for structure elucidation.","PeriodicalId":502957,"journal":{"name":"Jurnal Kimia Riset","volume":"48 9","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139185084","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Bell pepper can be an antioxidant and has many health benefits because of the high content of vitamin C. Vitamin C contents in yellow and orange bell peppers were extracted using different protic polar solvents and analyzed using the UV-Vis Spectrophotometry method. In this research, the bell peppers were extracted using the maceration technique for two days in 90% concentration of solvents (methanol and ethanol, respectively). Subsequently, the maximum wavelength was determined, and then 100 ppm ascorbic acid was used as a standard solution to analyze vitamin C content. Linearity based on a calibration curve is used to obtain the correlation coefficient of concentration between the standard solution and vitamin C levels in the sample. The result of UV-Vis spectroscopy analysis of this sample shows 373.5 nm of λmax. The linearity is shown in the equation y = 0.0006 x + 0.019. The vitamin C content in all samples had significant differences based on randomized complete block design (RCBD) test result with α = 0.05. The vitamin C level in the yellow pepper sample with an ethanol solvent (340 mg/100 g) was higher than that of the orange pepper sample with ethanol (251 mg/100 g). Meanwhile, the vitamin C content in the sample of yellow peppers with methanol solvent (562.5 mg/100 g) was smaller than that of orange peppers with methanol solvent (757.5 mg/100 g). These contents indicated a different result in the level sources of vitamin C, even if the maceration process used a solvent with a higher dielectric constant.
使用不同的原生极性溶剂萃取黄色和橙色甜椒中的维生素 C，并使用紫外可见分光光度法进行分析。在这项研究中，甜椒在浓度为 90% 的溶剂（分别为甲醇和乙醇）中浸泡两天后进行提取。然后，测定最大波长，再用 100 ppm 抗坏血酸作为标准溶液来分析维生素 C 的含量。根据校准曲线的线性关系，得出标准溶液与样品中维生素 C 含量之间的浓度相关系数。该样品的紫外可见光谱分析结果显示其 λmax 为 373.5 nm。线性方程为 y = 0.0006 x + 0.019。根据随机整群设计（RCBD）检验结果（α = 0.05），所有样品中的维生素 C 含量均有显著差异。乙醇溶剂黄椒样品中的维生素 C 含量（340 毫克/100 克）高于乙醇溶剂橙椒样品中的维生素 C 含量（251 毫克/100 克）。同时，甲醇溶剂黄椒样品中的维生素 C 含量（562.5 毫克/100 克）低于甲醇溶剂橙椒样品中的维生素 C 含量（757.5 毫克/100 克）。这些含量表明，即使浸渍过程中使用了介电常数较高的溶剂，维生素 C 的含量来源也是不同的。
{"title":"DETERMINATION OF VITAMIN C CONTENT IN BELL PEPPER (Capsicum annuum L.) WITH DIFFERENT PROTIC POLAR SOLVENT BY UV-VIS SPECTROSCOPY","authors":"Fawait Afnani, Jamilah Hamidi Yanti, W. Pratiwi","doi":"10.20473/jkr.v8i2.44865","DOIUrl":"https://doi.org/10.20473/jkr.v8i2.44865","url":null,"abstract":"Bell pepper can be an antioxidant and has many health benefits because of the high content of vitamin C. Vitamin C contents in yellow and orange bell peppers were extracted using different protic polar solvents and analyzed using the UV-Vis Spectrophotometry method. In this research, the bell peppers were extracted using the maceration technique for two days in 90% concentration of solvents (methanol and ethanol, respectively). Subsequently, the maximum wavelength was determined, and then 100 ppm ascorbic acid was used as a standard solution to analyze vitamin C content. Linearity based on a calibration curve is used to obtain the correlation coefficient of concentration between the standard solution and vitamin C levels in the sample. The result of UV-Vis spectroscopy analysis of this sample shows 373.5 nm of λmax. The linearity is shown in the equation y = 0.0006 x + 0.019. The vitamin C content in all samples had significant differences based on randomized complete block design (RCBD) test result with α = 0.05. The vitamin C level in the yellow pepper sample with an ethanol solvent (340 mg/100 g) was higher than that of the orange pepper sample with ethanol (251 mg/100 g). Meanwhile, the vitamin C content in the sample of yellow peppers with methanol solvent (562.5 mg/100 g) was smaller than that of orange peppers with methanol solvent (757.5 mg/100 g). These contents indicated a different result in the level sources of vitamin C, even if the maceration process used a solvent with a higher dielectric constant.","PeriodicalId":502957,"journal":{"name":"Jurnal Kimia Riset","volume":"5 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139185154","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Panduratin A is a prenylated flavonoid derivative from Boesenbergia pandurata with many potential biological activities. The biogenesis of this compound and its derivatives is believed to involve a Diels-Alder reaction between monoterpenoid and chalcone derivatives. This study provides insight into modeling biogenesis through the Diels-Alderreaction for Panduratin A and derivatives biosynthesis. We are using M06-2X/6-31G(d)//PM6 level of theory to explore the potential energy surfaces, asynchronicity degree, and global electron density transfer. Explicit water was applied to mimic physiological conditions. Contrary to the fact that water accelerates this reaction through hydrogen bonding catalysis, we found that water could slow this reaction. These results suggest that this reaction proceeds very slowly under physiological conditions, and enzymes catalyze this reaction.
Panduratin A 是一种产自 Boesenbergia pandurata 的前炔类黄酮衍生物，具有许多潜在的生物活性。这种化合物及其衍生物的生物生成过程被认为涉及单萜和查耳酮衍生物之间的 Diels-Alder 反应。本研究为通过 Diels-Alder 反应模拟 Panduratin A 及其衍生物的生物合成提供了深入的见解。我们使用 M06-2X/6-31G(d)/PM6 理论水平来探索势能面、异步度和全局电子密度转移。为了模拟生理条件，我们使用了显式水。与水通过氢键催化加速该反应的事实相反，我们发现水可以减缓该反应。这些结果表明，这一反应在生理条件下进行得非常缓慢，而酶催化了这一反应。
{"title":"WATER ROLE ON DIELS-ALDER REACTION OFPRENYLATED FLAVONOIDFORMATIONIN Boesenbergia pandurata: MECHANISM STUDY","authors":"Rahmanto Aryabraga Rusdipoetra, Kautsar Ul Haq","doi":"10.20473/jkr.v8i2.45215","DOIUrl":"https://doi.org/10.20473/jkr.v8i2.45215","url":null,"abstract":"Panduratin A is a prenylated flavonoid derivative from Boesenbergia pandurata with many potential biological activities. The biogenesis of this compound and its derivatives is believed to involve a Diels-Alder reaction between monoterpenoid and chalcone derivatives. This study provides insight into modeling biogenesis through the Diels-Alderreaction for Panduratin A and derivatives biosynthesis. We are using M06-2X/6-31G(d)//PM6 level of theory to explore the potential energy surfaces, asynchronicity degree, and global electron density transfer. Explicit water was applied to mimic physiological conditions. Contrary to the fact that water accelerates this reaction through hydrogen bonding catalysis, we found that water could slow this reaction. These results suggest that this reaction proceeds very slowly under physiological conditions, and enzymes catalyze this reaction.","PeriodicalId":502957,"journal":{"name":"Jurnal Kimia Riset","volume":"2 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139185233","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Wulan Safrihatini Atikah, Ikhwanul Muslim, Sandi Mu’min Pratama
The dyeing process with natural dyes has disadvantages, including poor color fastness. A mordanting process is required to overcome these disadvantages. Conventional mordanting processes often use metal salts. This research will substitute the mordanting process using surfactants as mordant substances. The pH of the process influences the application of dyeing with natural dyes. This study aims to determine the effect of the pre-mordant process using surfactants and the pH of the dyeing process on the color characteristics of cotton and silk fabrics dyed with Cocos nucifera L dye extract. The surfactants used were cationic and non-ionic polymeric surfactants. This study was conducted in phases. The first phase involved the extraction of coconut fiber, and the second phase involved pre-mordanting the fiber with surfactants. The third stage is the dyeing process, which has variations in pH 3, 7, and 9. The evaluation results show that cationic surfactants have the potential to be used as a mordant and provide an increased anti-bacterial effect on processed fabrics. The optimal use of cationic surfactants was obtained using a concentration of 9 g/L and pH 7 for the cotton dyeing process. The optimum concentration was obtained at 9 g/L for the silk dyeing process, and the dyeing pH was 3.
{"title":"THE EFFECT OF SURFACTANT ON PRE-MORDANTING AND pH OF DYEING PROCESS WITH NATURAL DYES","authors":"Wulan Safrihatini Atikah, Ikhwanul Muslim, Sandi Mu’min Pratama","doi":"10.20473/jkr.v8i2.49114","DOIUrl":"https://doi.org/10.20473/jkr.v8i2.49114","url":null,"abstract":"The dyeing process with natural dyes has disadvantages, including poor color fastness. A mordanting process is required to overcome these disadvantages. Conventional mordanting processes often use metal salts. This research will substitute the mordanting process using surfactants as mordant substances. The pH of the process influences the application of dyeing with natural dyes. This study aims to determine the effect of the pre-mordant process using surfactants and the pH of the dyeing process on the color characteristics of cotton and silk fabrics dyed with Cocos nucifera L dye extract. The surfactants used were cationic and non-ionic polymeric surfactants. This study was conducted in phases. The first phase involved the extraction of coconut fiber, and the second phase involved pre-mordanting the fiber with surfactants. The third stage is the dyeing process, which has variations in pH 3, 7, and 9. The evaluation results show that cationic surfactants have the potential to be used as a mordant and provide an increased anti-bacterial effect on processed fabrics. The optimal use of cationic surfactants was obtained using a concentration of 9 g/L and pH 7 for the cotton dyeing process. The optimum concentration was obtained at 9 g/L for the silk dyeing process, and the dyeing pH was 3.","PeriodicalId":502957,"journal":{"name":"Jurnal Kimia Riset","volume":"32 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139185037","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Kratom (Mitragyna speciosa Korth) is a tropical plant originating from Southeast Asia that predominantly contains alkaloid compounds and can potentially maintain levels of monoamine compounds in the body to treat depression. The study aimed to examine the potential of 8 alkaloid compounds in kratom as antidepressants towards four target proteins: Serotonin Transporter (SERT), Dopamine Transporter (DOPAT), Leucine Transporter (LEUT), and Monoamine Oxidase (MAO) via molecular docking. The Pyrx program is used with exhaustiveness 106 as the protocol, and the grid is adapted to the active site of each receptor. The affinity values of the alkaloid compounds in kratom are mitragynine, 7-hydroxy mitragynine, speciociliatine, paynantheine, speciogynine, corynantheidine, mitraciliatine, and 9-hydroxycorynantheidine, for MAO were -7.1, -6.1, -5.7, -6.7, -5.7, -7.7, -5.7, and -5.7 kcal/ mole. All compounds bind to amino acid residues in the target protein through hydrogen and pi (π) bonds. All the tested alkaloid compounds have the potential to be re-uptake inhibitors SERT, DOPAT, LEUT, and Monoamine Oxidase (MAO).
{"title":"STUDY MOLECULES DOCKING OF ALKALOIDS IN KRATOM ON SEROTONIN TRANSPORTER (SERT), NOREPINEPHRINE TRANSPORTER (NET), AND MONOAMINE OXIDASE (MAO)","authors":"Dandi Irawan, Bambang Wijianto, Harianto Ih","doi":"10.20473/jkr.v8i2.50785","DOIUrl":"https://doi.org/10.20473/jkr.v8i2.50785","url":null,"abstract":"Kratom (Mitragyna speciosa Korth) is a tropical plant originating from Southeast Asia that predominantly contains alkaloid compounds and can potentially maintain levels of monoamine compounds in the body to treat depression. The study aimed to examine the potential of 8 alkaloid compounds in kratom as antidepressants towards four target proteins: Serotonin Transporter (SERT), Dopamine Transporter (DOPAT), Leucine Transporter (LEUT), and Monoamine Oxidase (MAO) via molecular docking. The Pyrx program is used with exhaustiveness 106 as the protocol, and the grid is adapted to the active site of each receptor. The affinity values of the alkaloid compounds in kratom are mitragynine, 7-hydroxy mitragynine, speciociliatine, paynantheine, speciogynine, corynantheidine, mitraciliatine, and 9-hydroxycorynantheidine, for MAO were -7.1, -6.1, -5.7, -6.7, -5.7, -7.7, -5.7, and -5.7 kcal/ mole. All compounds bind to amino acid residues in the target protein through hydrogen and pi (π) bonds. All the tested alkaloid compounds have the potential to be re-uptake inhibitors SERT, DOPAT, LEUT, and Monoamine Oxidase (MAO).","PeriodicalId":502957,"journal":{"name":"Jurnal Kimia Riset","volume":"45 8","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139185425","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Free-living N2-fixing bacteria are essential in the soil because they provide a source of nitrogen in the form of ammonium needed by plants to be used in building protein blocks. The fixation of free N2 needs to be increased by adding nanomaterials such as magnetite (Fe3O4), which has an active group and can be a source of nitrogenase enzyme cofactor. In this study, increased N2 fixation used N2-fixing bacteria in Burks medium. This increase was determined by measuring NH3 levels using the Phenate method formed after Burks medium was treated with Fe3O4 and chitosan-magnetite (CS-Fe3O4). The study found that the number of bacteria can be well decreased. This research showed that using Fe3O4 and CS-Fe3O4 increased NH3-N levels in cultures of free-living nitrogen-fixing bacteria by 15.40% and 75.54%. For future development, it can be in the form of optimization, the effect of adding the same material to plant secondary metabolites, and the mechanism of bacteria in using the material.
{"title":"EFFECT OF MAGNETITE AND CHITOSAN-MAGNETITE ADDITION ON BACTERIAL LEVELS AND NH3-N (FREE-LIVING N2-FIXING BACTERIA CULTURE)","authors":"Ali Umar, Deden Saprudin, Fahrizal Hazra","doi":"10.20473/jkr.v8i2.47647","DOIUrl":"https://doi.org/10.20473/jkr.v8i2.47647","url":null,"abstract":"Free-living N2-fixing bacteria are essential in the soil because they provide a source of nitrogen in the form of ammonium needed by plants to be used in building protein blocks. The fixation of free N2 needs to be increased by adding nanomaterials such as magnetite (Fe3O4), which has an active group and can be a source of nitrogenase enzyme cofactor. In this study, increased N2 fixation used N2-fixing bacteria in Burks medium. This increase was determined by measuring NH3 levels using the Phenate method formed after Burks medium was treated with Fe3O4 and chitosan-magnetite (CS-Fe3O4). The study found that the number of bacteria can be well decreased. This research showed that using Fe3O4 and CS-Fe3O4 increased NH3-N levels in cultures of free-living nitrogen-fixing bacteria by 15.40% and 75.54%. For future development, it can be in the form of optimization, the effect of adding the same material to plant secondary metabolites, and the mechanism of bacteria in using the material.","PeriodicalId":502957,"journal":{"name":"Jurnal Kimia Riset","volume":"9 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139185086","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Hasri Tri Maya Saragih, Jhony Hartanta Sembiring, Elfrida Ginting
This study aims to determine the bioethanol yield and characteristics from pineapple peel with two methods such as Simultaneous Saccharification and Fermentation (SSF) and Separate Hydrolysis and Fermentation (SHF). The percent yield of bioethanol produced from the fermentation of pineapple peel (Ananas comosus) with the Simultaneous Saccharification and Fermentation method was 63.50%, while the yield of bioethanol from the Separate Hydrolysis and Fermentation method was 58.75%. The physical characteristics of bioethanol pineapple peel waste using Simultaneous Saccharification and Fermentation method has a density of 0.8237 w/v whilst with Separate Hydrolysis and Fermentation is 0.8858 w/v. Furthermore, viscosity of bioethanol using Simultaneous Saccharification and Fermentation is 1.05 Cp whereas using Separate Hydrolysis and Fermentation is 1.02 Cp. Pineapple peel bioethanol method of Simultaneous Saccharification and Fermentation has concentration of 13% while Separate Hydrolysis and Fermentation method has concentration of 7.92%. FTIR spectra from SHF bioethanol missing the peak correlated with CH, CH3, and CO. These missing peaks is due to the high percentage of water. Furthermore, bioethanol from SSF method showed peaks corresponding to CH, CH3, and CO functional groups. It can be concluded that SSF method give bioethanol with optimum result.
{"title":"CONVERSION OF PINEAPPLE PEEL GLUCOSE INTO BIOETHANOL USING SIMULTANEOUS SACCHARIFICATION AND FERMENTATION (SSF) METHOD AND SEPARATE HYDROLYSIS AND FERMENTATION (SHF) METHOD","authors":"Hasri Tri Maya Saragih, Jhony Hartanta Sembiring, Elfrida Ginting","doi":"10.20473/jkr.v8i2.50581","DOIUrl":"https://doi.org/10.20473/jkr.v8i2.50581","url":null,"abstract":"This study aims to determine the bioethanol yield and characteristics from pineapple peel with two methods such as Simultaneous Saccharification and Fermentation (SSF) and Separate Hydrolysis and Fermentation (SHF). The percent yield of bioethanol produced from the fermentation of pineapple peel (Ananas comosus) with the Simultaneous Saccharification and Fermentation method was 63.50%, while the yield of bioethanol from the Separate Hydrolysis and Fermentation method was 58.75%. The physical characteristics of bioethanol pineapple peel waste using Simultaneous Saccharification and Fermentation method has a density of 0.8237 w/v whilst with Separate Hydrolysis and Fermentation is 0.8858 w/v. Furthermore, viscosity of bioethanol using Simultaneous Saccharification and Fermentation is 1.05 Cp whereas using Separate Hydrolysis and Fermentation is 1.02 Cp. Pineapple peel bioethanol method of Simultaneous Saccharification and Fermentation has concentration of 13% while Separate Hydrolysis and Fermentation method has concentration of 7.92%. FTIR spectra from SHF bioethanol missing the peak correlated with CH, CH3, and CO. These missing peaks is due to the high percentage of water. Furthermore, bioethanol from SSF method showed peaks corresponding to CH, CH3, and CO functional groups. It can be concluded that SSF method give bioethanol with optimum result.","PeriodicalId":502957,"journal":{"name":"Jurnal Kimia Riset","volume":"15 6","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139185181","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The photocatalyst process involves light (photons) as an energy source and catalysts such as TiO2 to accelerate the reaction. Efforts are made to reduce the band gap energy of TiO2 by shifting the absorption towards visible light using metal cation doping, such as Ni2+, and they can float on the surface with coconut fiber. XRD characteristics with TiO2 diffractogram experienced a 2θ shift as an indication that Ni has entered the TiO2 structure and seen some peaks decreased in intensity after being embedded with coconut fiber as an indication that TiO2/Ni has successfully attached to the fiber. The band gap energy on TiO2 is 3.21 eV with a wavelength of 386.5 nm in UV light. TiO2/Ni-coconut fiber experienced a shift in band gap energy to 3.09 eV with a wavelength of 400.9 nm, which is in visible light. This indicates that Ni has successfully entered the TiO2 structure. The TiO2/Ni catalyst embraced with coconut fiber has a higher degradation activity than the catalyst without an embrainer, with a percent degradation of 28.66% for 120 minutes of irradiation. This is influenced by the amount of light that can be absorbed during the photocatalysis process.
{"title":"DEGRADATION OF TETRACYCLINE BY FLOATING PHOTOCATALYST TiO2/Ni-COCONUT FIBER","authors":"Lavena Imelda Putri, Deri Agustiawan, Didiek Sugandi, Khaizurani Arfida, Mardhatilla, Nelly Wahyuni","doi":"10.20473/jkr.v8i2.50848","DOIUrl":"https://doi.org/10.20473/jkr.v8i2.50848","url":null,"abstract":"The photocatalyst process involves light (photons) as an energy source and catalysts such as TiO2 to accelerate the reaction. Efforts are made to reduce the band gap energy of TiO2 by shifting the absorption towards visible light using metal cation doping, such as Ni2+, and they can float on the surface with coconut fiber. XRD characteristics with TiO2 diffractogram experienced a 2θ shift as an indication that Ni has entered the TiO2 structure and seen some peaks decreased in intensity after being embedded with coconut fiber as an indication that TiO2/Ni has successfully attached to the fiber. The band gap energy on TiO2 is 3.21 eV with a wavelength of 386.5 nm in UV light. TiO2/Ni-coconut fiber experienced a shift in band gap energy to 3.09 eV with a wavelength of 400.9 nm, which is in visible light. This indicates that Ni has successfully entered the TiO2 structure. The TiO2/Ni catalyst embraced with coconut fiber has a higher degradation activity than the catalyst without an embrainer, with a percent degradation of 28.66% for 120 minutes of irradiation. This is influenced by the amount of light that can be absorbed during the photocatalysis process.","PeriodicalId":502957,"journal":{"name":"Jurnal Kimia Riset","volume":"10 5","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139185320","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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