1. 江南大学生物工程学院工业生物技术教育部重点实验室,江苏 无锡 214122 2. 无锡格莱克斯生物科技有限公司,江苏 无锡 214125
收稿日期:
2018-11-09修回日期:
2018-12-26出版日期:
2019-08-22发布日期:
2019-08-15通讯作者:
高敏杰基金资助:
国家自然科学基金(极高细胞密度下乙醇历史积累抑制毕赤酵母表达外源蛋白的分子机制及解抑制策略研究);江南大学自主科研计划-重点项目(高粘度、高密度发酵过程关键技术与装备);江苏省政策引导类计划(产学研合作)-前瞻性联合研究项目(毕赤酵母高效吸附稀贵金属离子关键技术研发及产业化)Direct production of curdlan oligosaccharides by coupled fermentation system of Agrobacterium sp.-Pichia pastoris
Feifei LI1, Shuxia JIN1, Li ZHU2, Xiaobei ZHAN1, Yue ZHAO1, Liping LIU1, Minjie GAO1*1. Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi, Jiangsu 214122, China 2. Wuxi Glyco Biotechology Co., Ltd., Wuxi, Jiangsu 214125, China
Received:
2018-11-09Revised:
2018-12-26Online:
2019-08-22Published:
2019-08-15摘要/Abstract
摘要: 为提高热凝胶低聚糖生产效率,构建了土壤杆菌?毕赤酵母耦合培养体系,其中土壤杆菌代谢产物热凝胶可被毕赤酵母分泌的内切-?-1,3-葡聚糖酶利用直接生产热凝胶低聚糖。用基于不同启动子(AOX1, GAP, FLD)调控的毕赤酵母重组菌株分泌表达内切-β-1,3-葡聚糖酶BGN13.1a,验证其均能有效水解热凝胶得到热凝胶低聚糖。在此基础上,选取GAP启动子调控的毕赤酵母工程菌与土壤杆菌耦合培养,通过设计两种物种之间的共生关系实现稳定共培养并生产聚合度为17?22的热凝胶低聚糖,产量为4.278 g/L。
引用本文
李菲菲 金树霞 朱莉 詹晓北 赵玥 刘丽萍 高敏杰. 土壤杆菌-毕赤酵母耦合培养直接生产热凝胶低聚糖[J]. 过程工程学报, 2019, 19(4): 801-808.
Feifei LI Shuxia JIN Li ZHU Xiaobei ZHAN Yue ZHAO Liping LIU Minjie GAO. Direct production of curdlan oligosaccharides by coupled fermentation system of Agrobacterium sp.-Pichia pastoris[J]. Chin. J. Process Eng., 2019, 19(4): 801-808.
使用本文
导出引用管理器 EndNote|Ris|BibTeX
链接本文:http://www.jproeng.com/CN/10.12034/j.issn.1009-606X.218319
http://www.jproeng.com/CN/Y2019/V19/I4/801
参考文献
[1] 张洪涛,詹晓北,郑志永,等. 热凝胶的高产策略及功能研究进展 [J]. 生物加工过程, 2009, 7(5):8-12. Zhang HT, Zhan XB, Zheng ZY. et al. Advances in curdlan of production by Alcaligenes faecalis and function of curdlan [J]. Chinese Journal of Bioprocess Engineering, 2009, 7(5):8-12. [2] Jamois F, Ferrieres V, Guegan JP, et al. Glucan-like synthetic oligosaccharides: iterative synthesis of linear oligo-beta-(1,3)-glucans and immunostimulatory effects [J]. Glycobiology, 2005, 15(4):393-407. [3] Miyanishi N, Iwamoto Y, Watanabe E, et al. Induction of TNF-alpha production from human peripheral blood monocytes with beta-1,3-glucan oligomer prepared from laminarin with beta-1,3-glucanase from Bacillus clausii NM-1 [J]. J Biosci Bioeng, 2003, 95(2):192-195. [4] Fu YB, Yin H, Wang WX, Wang MY, et al. beta-1,3-Glucan with different degree of polymerization induced different defense responses in tobacco [J]. Carbohydr Polym, 2011, 86(2):774-782. [5] 李晶. 热凝胶制备β-1,3-葡聚寡糖及其诱导抗真菌功能的研究 [D]. 江南大学; 2014. [6] 徐敏,李晶,郑志永,等. 哈茨木霉产水解热凝胶的内切β-1,3-葡聚糖酶的分离纯化 [J]. 食品工业科技, 2014, 35(12):157-161. Xu M, Li J, Zheng ZY, et al. Purification of an endo-β-1,3-glucanase to degrade curdlan from Trichoderma harzianum [J]. Science and Technology of Food Industry, 2014, 35(12):157-161. [7] Liang Y, Zhu L, Gao M, et al. Effective production of biologically active water-soluble beta-1,3-glucan by a coupled system of Agrobacterium sp. and Trichoderma harzianum [J]. Prep Biochem Biotechnol, 2018, 48(5):446-456. [8] 李珊. 哈茨木霉发酵生产内切β-1,3-葡聚糖酶的工艺研究 [D]. 江南大学; 2014. [9] Zhang H, Wang X. Modular co-culture engineering, a new approach for metabolic engineering [J]. Metab Eng, 2016, 37:114-121. [10] Zhou K, Qiao K, Edgar S, et al. Distributing a metabolic pathway among a microbial consortium enhances production of natural products [J]. Nat Biotechnol, 2015, 33(4):377-383. [11] J.Minty J, Singer ME, A.Scholz S, et al. Design and characterization of synthetic fungal-bacterial consortia for direct production of isobutanol from cellulosic biomass [J]. Proc Natl Acad Sci USA, 2013, 110(36):14592-14597. [12] Saini M, Chen MH, Chung-Jen C, et al. Potential production platform of n-butanol in Escherichia coli [J]. Metab Eng, 2015, 27:76-82. [13] Saini M, Chiang CJ, Li SY, et al. Production of biobutanol from cellulose hydrolysate by the Escherichia coli co-culture system [J]. FEMS Microbiol Lett, 2016, 363(4):fnw008. [14] Zhang H, Pereira B, Li Z, Stephanopoulos G. Engineering Escherichia coli coculture systems for the production of biochemical products [J]. Proc Natl Acad Sci USA, 2015, 112(27):8266-8271. [15] Zhang H, Stephanopoulos G. Co-culture engineering for microbial biosynthesis of 3-amino-benzoic acid in Escherichia coli [J]. Biotechnol. J., 2016, 11(7):981-987. [16] Wang EX, Ding MZ, Ma Q, et al. Reorganization of a synthetic microbial consortium for one-step vitamin C fermentation [J]. Microb Cell Fact, 2016, 15:21. [17] Daly R, Hearn MT. Expression of heterologous proteins in Pichia pastoris: a useful experimental tool in protein engineering and production [J]. J Mol Recognit, 2005, 18(2):119-138. [18] Ahmad M, Hirz M, Pichler H, et al. Protein in Pichia pastoris: recent achievements and perspectives for heterologous protein production [J]. Appl Microbiol Biotechnol, 2014, 98(12):5301-5317. [19] 郭美锦,朱泰承,张明,等. 重组毕赤酵母甲醇利用表型与基因拷贝数对外源基因表达的影响 [J]. 中国生物工程杂志, 2007, 27(7),7-11. Guo MJ, Zhu TC, Zhang M, et al. Influences of Methanol Utilization Phenotype and Gene Dosage on Heterologous Protein Expression in Recombinant Pichia pastoris [J]. Journal of Chinese Biotechnology, 2007, 27(7),7-11. [20] Ellis SB, Brust PF, Koutz PJ, et al. Isolation of alcohol oxidase and two other methanol regulatable genes from the yeast Pichia pastoris [J]. Mol Cell Biol, 1985, 5(5):1111-1121. [21] Waterham HR, Digan ME, Koutz PJ, et al. Isolation of the Pichia pastoris glyceraldehyde-3-phosphate dehydrogenase gene and regulation and use of its promoter. Gene, 1997, 186(1):37-44. [22] Shen SG, Sulter G, Jeffries TW, et al. A strong nitrogen source-regulated promoter for controlled of foreign genes in the yeast Pichia pastoris [J]. Gene, 1998, 216(1):93-102. |
相关文章 6
[1] | 刘羽珊李强. 单启动子双拷贝CPC酰化酶基因在毕赤酵母中的表达[J]. , 2014, 14(3): 476-481. |
[2] | 金赛徐俭张梁丁重阳石贵阳. 根癌土壤杆菌产辅酶Q10的补料分批发酵工艺[J]. , 2011, 11(1): 113-116. |
[3] | 周进银鹏. 葡萄糖苷酶在毕赤酵母中的重组表达及一步纯化[J]. , 2009, 9(5): 981-986. |
[4] | 金虎徐俊高敏杰段作营李震刘立明史仲平. 多变量在线测量条件下的猪α干扰素高效表达[J]. , 2009, 9(3): 563-567. |
[5] | 张宏斌;窦文芳;许泓瑜;金坚;李华钟;许正宏. 提高重组毕赤酵母表达hIFNb-HSA的碳源控制策略[J]. , 2007, 7(6): 1181-1186. |
[6] | 马善康;李强;顾小勇. 双碳源交替刺激毕赤酵母高效表达人尿激酶原[J]. , 2002, 2(5): 0-0. |
PDF全文下载地址:
http://www.jproeng.com/CN/article/downloadArticleFile.do?attachType=PDF&id=3298