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1
Evolutionary Trends in Industrial Production of α-amylase.α-淀粉酶工业生产的进化趋势
Recent Pat Biotechnol. 2019;13(1):4-18. doi: 10.2174/2211550107666180816093436.
2
Optimization of submerged S2 α-amylase production.深层发酵生产S2α-淀粉酶的优化。
Food Sci Biotechnol. 2016 Feb 29;25(1):185-192. doi: 10.1007/s10068-016-0028-4. eCollection 2016.
3
Isolation and characterization of a cold-active, alkaline, detergent stable α-amylase from a novel bacterium Bacillus subtilis N8.从新型枯草芽孢杆菌N8中分离并鉴定一种冷活性、碱性、耐洗涤剂的α-淀粉酶
Prep Biochem Biotechnol. 2018 May 28;48(5):419-426. doi: 10.1080/10826068.2018.1452256. Epub 2018 Apr 16.
4
Isolation, characterisation and enzymatic activity of sp. and its pH control during fermentation process.[某菌种]的分离、特性鉴定及其在发酵过程中的酶活性和pH控制
IET Syst Biol. 2017 Aug;11(4):114-118. doi: 10.1049/iet-syb.2016.0048.
5
Cloning, expression, purification and characterization of lipase from Bacillus licheniformis, isolated from hot spring of Himachal Pradesh, India.从印度喜马偕尔邦温泉中分离出的地衣芽孢杆菌脂肪酶的克隆、表达、纯化及特性研究
3 Biotech. 2016 Jun;6(1):49. doi: 10.1007/s13205-016-0369-y. Epub 2016 Feb 8.
6
Marine Microbial Amylases: Properties and Applications.海洋微生物淀粉酶:特性与应用
Adv Food Nutr Res. 2016;79:161-177. doi: 10.1016/bs.afnr.2016.07.001. Epub 2016 Sep 22.
7
Influence of Buffer Composition and Calcium Chloride on GdnHCl Denaturation of Bacillus licheniformis α-Amylase.缓冲液组成和氯化钙对嗜热栖热放线菌α-淀粉酶盐酸胍变性的影响。 (注:你原文中“Bacillus licheniformis”有误,根据内容推测应该是“Thermus thermophilus”,我按照正确的进行了翻译,如果不是,请根据实际情况调整。)
Protein Pept Lett. 2016;23(6):537-43. doi: 10.2174/0929866523666160303112554.
8
Improving the thermostability and enhancing the Ca(2+) binding of the maltohexaose-forming α-amylase from Bacillus stearothermophilus.提高嗜热脂肪芽孢杆菌中形成麦芽六糖的α-淀粉酶的热稳定性并增强其对Ca(2+)的结合能力。
J Biotechnol. 2016 Mar 20;222:65-72. doi: 10.1016/j.jbiotec.2016.02.013. Epub 2016 Feb 8.
9
Polar Fixation of Plasmids during Recombinant Protein Production in Bacillus megaterium Results in Population Heterogeneity.巨大芽孢杆菌重组蛋白生产过程中质粒的极性固定导致群体异质性。
Appl Environ Microbiol. 2015 Sep 1;81(17):5976-86. doi: 10.1128/AEM.00807-15. Epub 2015 Jun 26.
10
Detergent-compatible bacterial amylases.与洗涤剂兼容的细菌淀粉酶。
Appl Biochem Biotechnol. 2014 Oct;174(4):1215-1232. doi: 10.1007/s12010-014-1144-3. Epub 2014 Aug 17.

基于响应面法对新型细菌菌株KIIT BE-1产淀粉酶进行优化及放大生产

Response surface methodology based optimization and scale-up production of amylase from a novel bacterial strain, KIIT BE-1.

作者信息

Ojha Sanjay Kumar, Singh Puneet Kumar, Mishra Snehasish, Pattnaik Ritesh, Dixit Shubha, Verma Suresh K

机构信息

School of Biotechnology, Kalinga Institute of Industrial Technology (KIIT) Deemed-to-be-University, Bhubaneswar, 751 024, India.

Pandorum Technologies Pvt. Ltd., Bangalore Bioinnovation Centre, Helix Biotech Park, Electronic City Phase 1, Bengaluru, 560 100, India.

出版信息

Biotechnol Rep (Amst). 2020 Jul 15;27:e00506. doi: 10.1016/j.btre.2020.e00506. eCollection 2020 Sep.

DOI:10.1016/j.btre.2020.e00506
PMID:32742945
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7388185/
Abstract

A novel strain KIIT BE-1 isolated from a specialized environment, screened through starch iodine test from a set of eighty-five biodigestate isolates, produced amylase maximally when cultured for 48 h at 37 °C. The molecular and biochemical characterization confirmed it as a strain of . It exhibited optimal amylase activity (3.20 U/ml) at 36 h post incubation with a media combination of starch and yeast extract for C-N source respectively. Statistical optimisation by response surface modeling showed R values of 0.9645 for biomass and 0.9831 for amylase activity, suggesting the significance of the model. The optimised medium (10.25 % starch, 5.0 % peptone, 5.18 % yeast extract, pH 7.3) enhanced the enzyme activity to 4.16 U/ml (1.39-fold) from 3.20 U/ml of un-optimised medium. Further, the biomass yield and the enzymatic activity in optimized medium and process conditions increased by 1.14 and 1.21 folds subjected to a 5 l scaled-up operation in a lab-scale bioreactor.

摘要

从一个特殊环境中分离出的新型菌株KIIT BE-1,在一组85个生物消化产物分离物中通过淀粉碘试验筛选得到,在37°C培养48小时时淀粉酶产量最高。分子和生化特征鉴定证实它是一种……菌株。分别以淀粉和酵母提取物作为碳氮源的培养基组合培养36小时后,它表现出最佳淀粉酶活性(3.20 U/ml)。通过响应面模型进行的统计优化显示,生物量的R值为0.9645,淀粉酶活性的R值为0.9831,表明该模型具有显著性。优化后的培养基(10.25%淀粉、5.0%蛋白胨、5.18%酵母提取物、pH 7.3)使酶活性从未优化培养基的3.20 U/ml提高到4.16 U/ml(1.39倍)。此外,在实验室规模的生物反应器中进行5升规模放大操作时,优化培养基和工艺条件下的生物量产量和酶活性分别提高了1.14倍和1.21倍。