| Producing hyperactive amyloglucosidase involves preparing an induced Aspergillus niger culture by incubation, creating a substrate mixture by mixing wheat bran or oat bran, Czapek-Dox media, and whey protein, autoclaving substrate mixture and inoculating autoclaved substrate with induced inoculum | |
| 2024-02-27 | |
| 专利权人 | INDIAN INST TECHNOLOGY KHARAGPUR (IIKH-C) |
| 申请日期 | 2024-02-27 |
| 专利号 | IN202431014189-A |
| 成果简介 | NOVELTY - Producing hyperactive amyloglucosidase involves: (a) preparing an induced Aspergillus niger culture with an incubation duration ranging from 60 hours to 170 hours; (b) creating a substrate mixture by mixing wheat bran or oat bran, Czapek-Dox media, and whey protein in a ratio ranging from 1:1:1 to 4:2:1; (c) autoclaving the substrate mixture at any temperature ranging from 117℃ to 125℃ for a period of 30 minutes; (d) inoculating the autoclaved substrate with induced inoculum of Aspergillus niger culture at a maximum concentration of 10 wt.%/vol.%; (e) incubating the inoculated substrate at a temperature ranging from 15℃ to 45℃ for a period of 60 hours to 170 hours for producing fermented biomass; (f) mixing the fermented biomass obtained after incubation with distilled water in a ratio of 1:4; (g) incubating the mixture of fermented biomass and distilled water for a period of 2 hours at a room temperature. USE - Method for producing hyperactive amyloglucosidase. ADVANTAGE - The method is safe, biodegradable and environment friendly. The produced amyloglucosidase has an improved half-life and shelf life extended to more than 24 months at 4℃ making it suitable for long-term applications. The enzyme activity in the hyperactive amyloglucosidase is quantified using a spectrophotometric assay. DETAILED DESCRIPTION - Producing hyperactive amyloglucosidase involves: (a) preparing an induced Aspergillus niger culture with an incubation duration ranging from 60 hours to 170 hours; (b) creating a substrate mixture by mixing wheat bran or oat bran, Czapek-Dox media, and whey protein in a ratio ranging from 1:1:1 to 4:2:1; (c) autoclaving the substrate mixture at any temperature ranging from 117℃ to 125℃ for a period of 30 minutes; (d) inoculating the autoclaved substrate with induced inoculum of Aspergillus niger culture at a maximum concentration of 10 wt.%/vol.%; (e) incubating the inoculated substrate at a temperature ranging from 15℃ to 45℃ for a period of 60 hours to 170 hours for producing fermented biomass; (f) mixing the fermented biomass obtained after incubation with distilled water in a ratio of 1:4; (g) incubating the mixture of fermented biomass and distilled water for a period of 2 hours at a room temperature; (h) extracting the enzyme by filtering the mixture through cheesecloth; and (i) centrifuging the filtrate enzyme to obtain the hyperactive amyloglucosidase. |
| IPC 分类号 | C12N-001/14 ; C12N-009/24 |
| 国家 | 印度 |
| 专业领域 | 化学化工 |
| 语种 | 英语 |
| 成果类型 | 专利 |
| 文献类型 | 科技成果 |
| 条目标识符 | http://119.78.100.226:8889/handle/3KE4DYBR/17980 |
| 专题 | 中国科学院新疆生态与地理研究所 |
| 作者单位 | INDIAN INST TECHNOLOGY KHARAGPUR (IIKH-C) |
| 推荐引用方式 GB/T 7714 | DUTTA S,RAJLAKSHMI,JAYASEELAN P,et al. Producing hyperactive amyloglucosidase involves preparing an induced Aspergillus niger culture by incubation, creating a substrate mixture by mixing wheat bran or oat bran, Czapek-Dox media, and whey protein, autoclaving substrate mixture and inoculating autoclaved substrate with induced inoculum. IN202431014189-A[P]. 2024. |
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