High level extracellular production of a truncated alkaline beta-mannanase from alkaliphilic Bacillus sp N16-5 in Escherichia coli by the optimization of induction condition and fed-batch fermentation
文献类型:期刊论文
作者 | Zheng, Hongchen1,2; Yu, Zhenxiao1,2; Fu, Xiaoping1,2; Li, Shufang1,2; Xu, Jianyong1,2; Song, Hui1,2; Ma, Yanhe1 |
刊名 | JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY
![]() |
出版日期 | 2016-07-01 |
卷号 | 43期号:7页码:977-987 |
关键词 | Alkaline beta-mannanase Truncation Escherichia coli Triton X-100 One-time feeding |
英文摘要 | To improve the extracellular production of alkaline beta-mannanase from alkaliphilic Bacillus sp. N16-5 in Escherichia coli, two truncated recombinant mannanases (32a-ManAR2 and 22b-ManAR2) were obtained. Compared with the full-length mannanases (32a-ManAR1 and 22b-ManAR1), the truncated mannanases not only showed higher secretion rate, but also exhibited higher thermostability and alkalistability. The K-m value (11 mg/mL) of 32a-ManAR2 was higher than that (1.46 mg/mL) of 32a-ManAR1. The specific activity of 22b-ManAR2 was 2.7 times higher than that of 22b-ManAR1. 22b-ManAR2 showed the highest k(cat)/K-m value of 602.7 ml/mg s. The parameters of induction for recombinant mannanase production of E. coli BL21 (pET32a-manAR2) and E. coli BL21 (pET22b-manAR2) were subsequently optimized. The yield of soluble mannanase was found to be enhanced with lower induction temperature (25 degrees C), lower IPTG concentration (0.01-0.05 mM), and Triton X-100 supplement (0.1 %) in a shake flask. Moreover, a one-time feeding strategy and Triton X-100 supplement were applied in production of 22b-ManAR2 in a 10 L fermentor. The productivity of the total soluble mannanase reached 9284.64 U/mL with the extracellular rate of 74 % at 46 h of fermentation, which was the highest productive level of alkaline beta-mannanase in recombinant E. coli to date. |
WOS标题词 | Science & Technology ; Life Sciences & Biomedicine |
类目[WOS] | Biotechnology & Applied Microbiology |
研究领域[WOS] | Biotechnology & Applied Microbiology |
关键词[WOS] | PICHIA-PASTORIS ; GENE CLONING ; EXPRESSION ; PULLULANASE ; STRATEGY |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000379625600008 |
源URL | [http://124.16.173.210/handle/834782/2912] ![]() |
专题 | 天津工业生物技术研究所_基因工程与微生物应用技术研究组 宋恢_期刊论文 |
作者单位 | 1.Chinese Acad Sci, Tianjin Inst Ind Biotechnol, Ind Enzymes Natl Engn Lab, Tianjin 300308, Peoples R China 2.Chinese Acad Sci, Tianjin Inst Ind Biotechnol, Tianjin Key Lab Ind Biol Syst & Bioproc Engn, 32 XiQiDao,Tianjin Airport Econ Pk, Tianjin 300308, Peoples R China |
推荐引用方式 GB/T 7714 | Zheng, Hongchen,Yu, Zhenxiao,Fu, Xiaoping,et al. High level extracellular production of a truncated alkaline beta-mannanase from alkaliphilic Bacillus sp N16-5 in Escherichia coli by the optimization of induction condition and fed-batch fermentation[J]. JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY,2016,43(7):977-987. |
APA | Zheng, Hongchen.,Yu, Zhenxiao.,Fu, Xiaoping.,Li, Shufang.,Xu, Jianyong.,...&Ma, Yanhe.(2016).High level extracellular production of a truncated alkaline beta-mannanase from alkaliphilic Bacillus sp N16-5 in Escherichia coli by the optimization of induction condition and fed-batch fermentation.JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY,43(7),977-987. |
MLA | Zheng, Hongchen,et al."High level extracellular production of a truncated alkaline beta-mannanase from alkaliphilic Bacillus sp N16-5 in Escherichia coli by the optimization of induction condition and fed-batch fermentation".JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY 43.7(2016):977-987. |
入库方式: OAI收割
来源:天津工业生物技术研究所
浏览0
下载0
收藏0
其他版本
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。