Please wait a minute...

中国生物工程杂志

China Biotechnology
China Biotechnology  2017, Vol. 37 Issue (8): 15-22    DOI: 10.13523/j.cb.20170803
    
Comparison of Signal Peptides for Two Hemicellulase Secretory Expression
YANG Qing1, WANG Bin1, WANG Ya-wei1, ZHANG Hua-shan2, XIONG Hai-rong1, ZHANG Li1
1. College of Life Science, South-Central University for Nationalities, Wuhan 430074, China;
2. Key Laboratory of Fermentation Engineering, Ministry of Education, Hubei University of Technology, Wuhan 430068, China
Download: HTML   PDF(874KB) HTML
Export: BibTeX | EndNote (RIS)      

Abstract  Xylanase and mannanase are two hemicellulases, which are widely used in many fields.To improve the expression of thermostable xylanase DSB and thermostable mannanase ManA in Pichia pastoris, three endogenous signal peptides of Pichia pastoris(Scw11, Dse4 and Exg1) were chosed. Their capability to mediate the secretion of DSB and ManA with that of the Saccharomyces cerevisiae α-factor were compared. In shake-flask cultivation, three endogenous signal peptides and α-factor efficiently mediated the secretion of DSB and ManA, but the secretion efficiency has obvious difference. As for DSB,the expression efficiency of α-factor was much higher than three endogenous signal peptides. But as for ManA, the expression efficiency of Dse4 was equal to α-factor and much higher than Scw11 and Exg1. Therefore,α-factoris the most efficient signal peptide for DSB expression and Dse4 or α-factor are the most efficient signal peptide for ManA expression in Pichia pastoris X33.Moreover,the intracellular activities of DSB and ManA by α-factor are higher than Scw11, Dse4 and Exg1, and the intracellular activity of ManA was higher than DSB (the molecular weight of ManA was larger than DSB).Thus, when ManA were expressed in Pichia pastoris, different signal peptide, such as Dse4, could be used for improving the secretion efficiency.A basis for identifying more available signal peptides and screening for the optimal signal peptide for the target protein was provided.

Key wordsMannanase (ManA)      Pichia pastoris      Signal peptide      Xylanase (DSB)     
Received: 27 February 2017      Published: 25 August 2017
ZTFLH:  Q819  
Cite this article:

YANG Qing, WANG Bin, WANG Ya-wei, ZHANG Hua-shan, XIONG Hai-rong, ZHANG Li. Comparison of Signal Peptides for Two Hemicellulase Secretory Expression. China Biotechnology, 2017, 37(8): 15-22.

URL:

https://manu60.magtech.com.cn/biotech/10.13523/j.cb.20170803     OR     https://manu60.magtech.com.cn/biotech/Y2017/V37/I8/15

[1] 陈威威,江正强,王瑞君.绵毛嗜热丝孢菌木聚糖酶对面包品质的改善.食品与发酵工业,2008,34(12):1-4. Chen W W,Jiang Z Q,Wang R J.Effect of a thermostable xylanase from thermomyces lanuginosus on bread quality.Food and Fermentation Industries,2008,34(12):1-4.
[2] 张金伟.甘露聚糖酶对动物生产性能的影响.饲料工业,2016,37(12):62-64. Zhang J W.Effects of the β-mannanase on the production performance of animals.Feed Industry,2016,37(12):62-64.
[3] 郝涤非.木聚糖酶及其复合酶在面包生产中的应用与探索.中国酿造,2008,27(16):77-80. Hao D F.Application and exploration of xylanaseandrelatedcompoundenzymeinbreadproduction.China Brewing, 2008, 27(16):77-80.
[4] 杨少杰,高海有,李晞,等.甘露聚糖酶和木聚糖酶在纸浆漂白中的应用.造纸科学与技术,2016,35(4):71-76. Yang S J, Gao H Y, Li X,et al.Application of mannanase and xylanase in the pulp bleaching.PaperScience&Technology,2016,35(4):71-76.
[5] 王冶,郑甲,唐诗哲,等.外源蛋白在巴斯德毕赤酵母中高效分泌表达的前沿技术. 基因组学与应用生物学,2014,33(3):689-694. Wang Y, Zheng J, Tang S Z, et al.Advance technologies of the efficient secretory expression of heterologous proteins in Pichia pastoris.Genomics and Applied Biology,2014,33(3):689-694.
[6] Su L, Xu C, Woodard R W,et al. A novel strategy for enhancing extracellular secretion of recombinant proteins in Escherichia coli. Applied Microbiology and Biotechnology,2013,97(15):6705-6713.
[7] Li S, Sing S, Wang Z.Improved expression of Rhizopus oryzae α-amylase in the methylotrophic yeast Pichia pastoris. Protein Expression & Purification,2011, 79(1):142-148.
[8] 石艺平,周雪,胡美荣,等. 不同信号肽对毕赤酵母表达漆酶的影响.微生物学报,2014,54(12):1446-1452. Shi Y P, Zhou X, Hu M R, et al..Effect of signal peptides on the expression of laccase in Pichia pastoris.Acta Microbiologica Sinica, 2014,54(12):1446-1452.
[9] Shen M,Wang Q,Mu X,et al. Expression,purification and characterization of recombinant human beta-amyloid 1-42 in Pichia pastoris. Protein Expr Purif, 2009,63(2):84-88.
[10] Richter S, Nieveler J, Schulze H,et al. High yield production of a mutant Nippostrongylus brasiliensis acetylcholinesterase in Pichia pastoris and its purification. BiotechnolBioeng, 2006,93(5):1017-1022.
[11] Daly R,Hearn M T. Expression of heterologous proteins in Pichia pastoris:a useful experimental tool in protein engineering and production. Journal of Molecular Recognition,2005,18(2):119-138.
[12] Wege S, Khan G A, Jung J Y,et al.The EXS domain of PHO1 participates in the response of shoots to phosphate deficiency via a root-to-shoot signal. Plant Physiology,2016, 170(1):385-400.
[13] Sun Q, Wang J S, Li R,et al. Establishment of suc2 signal sequence trap system.ActaGeneticaSinica, 2001, 28(4):379-384.
[14] Liang S L, Li C, Ye Y R,et al.Endogenous signal peptides efficiently mediate the secretion of recombinant proteins in Pichia pastoris.BiotechnolLett, 2013, 35(1):97-105.
[15] 李思佳,王亚伟,付正,等.嗜热真菌木聚糖酶1YNA及其双硫键突变体在毕赤酵母中的表达.中国生物工程杂志,2013,33(3):74-79. Li S J,Wang Y W,Fu Z,et al.Expression of thermomyces lanuginosus xylanase 1YNA and its disulphide bridge mutantin Pichia pastoris.China Biotechnology,2013,33(3):74-79.
[16] 张巍,王亚伟,陈丰,等.一株全基因合成耐热甘露聚糖酶的表达及酶学性质分析.中国生物工程杂志,2014,34(8):41-46. Zhang W, Wang Y W, Chen F, et al.Gene synthesis,expression and characterization of a thermostable endo-β-1,4-mannanase.China Biotechnology,2014,34(8):41-46.
[17] Wang Y W, Shi P J, Luo H Y, et al. Cloning, over-expression and characterization of an alkali-tolerant endo-β-1,4-mannanase from Penicillium freii F63. Journal of Bioscience and Bioengineering,2012,113(6):710-714.
[18] Bharuthram A, Paximadis M, Picton A C, et al. Comparison of a quantitative Real-Time PCR assay and droplet digital PCR for copy number analysis of the CCL4L genes. Infection, Genetics and Evolution, 2014, 25(7):28-35.
[19] 余红英,孙远明,王炜军,等.枯草芽孢杆菌SA-22β-甘露聚糖酶的纯化及其特性.生物工程学报,2003,19(3):327-331. Yu H Y, Sun Y M,Wang W J, et al.Purification and properties of Bacillus subtilis SA-22 endo-1,4-β-D-mannanase.Chinese Journal of Biotechnology,2003,19(3):327-331.
[20] 易弋,容元平,程谦伟,等.不同破壁方法提取酵母菌总RNA的比较.食品科学, 2011, 32(11):161-164. Yi G, Rong Y P, Cheng Q W, et al. Comparison of different cell wall disruption methods for yeast total RNA extraction.Food Science,2011, 32(11):161-164.
[21] Orna E,Tsaffrir Z. Linearization of the bradford protein assay. Journal of Visualized Experiments,2010, 38(38):1918.
[1] HE Ruo-yu,LIN Fu-yu,GAO Xiang-dong,LIU Jin-yi. Research and Application Progress of Signal Peptides in Escherichia coli Secretion Systems[J]. China Biotechnology, 2021, 41(5): 87-93.
[2] CHEN Zhong-wei,ZHENG Pu,CHEN Peng-cheng,WU Dan. Screening and Characterization of Thermostable Phytase Mutants[J]. China Biotechnology, 2021, 41(2/3): 30-37.
[3] CHEN Xin-jie,QIAN Zhi-lan,LIU Qi,ZHAO Qing,ZHANG Yuan-xing,CAI Meng-hao. Modification of Aromatic Amino Acid Synthetic Pathway in Pichia pastoris to Produce Cinnamic Acid and ρ-Coumaric Acid[J]. China Biotechnology, 2021, 41(10): 52-61.
[4] SHI Peng-cheng, JI Xiao-jun. Advances in Expression of Human Epidermal Growth Factor in Yeast[J]. China Biotechnology, 2021, 41(1): 72-79.
[5] Yuan TIAN,Yan-ling LI. Biosynthesis of Fusaruside Based on Recombinant Pichia pastoris[J]. China Biotechnology, 2019, 39(7): 8-14.
[6] Qiang-qiang PENG,Qi LIU,Ming-qiang XU,Yuan-xing ZHANG,Meng-hao CAI. Heterologous Expression of Insulin Precursor in A Newly Engineered Pichia pastoris[J]. China Biotechnology, 2019, 39(7): 48-55.
[7] AN Ming-hui,TIAN Wen,HAN Xiao-xu,SHANG Hong. Construction and Phenotypic Analyses of Recombinant Lactobacillus Expressing Single-Chain Antibody of HIV[J]. China Biotechnology, 2019, 39(10): 1-8.
[8] Gong CHENG,Si-ming JIAO,Li-shi REN,Cui FENG,Yu-guang DU. Preparation and Composition Analysis of Chitooligosaccharides with Low Degree of Deacetylation by Hydrolysis of Bacillus subtilis Chitosanase[J]. China Biotechnology, 2018, 38(9): 19-26.
[9] Nan WANG,Lv-hua JIN,Ling ZHANG,Rong LIN,Hai-lin YANG. The Effect of Signal Peptides on the Expression of Leucine Dehydrogenase and Enzymatic Properties in Bacillus subtilis[J]. China Biotechnology, 2018, 38(4): 46-53.
[10] ZHANG Ling,WANG Nan,JIN Lv-hua,LIN Rong,YANG Hai-lin. To Promote the Expression of Leucine Dehydrogenase in Bacillus subtilis via Dual-Promoter and Fermentation Research[J]. China Biotechnology, 2018, 38(12): 21-31.
[11] Si-ming JIAO,Gong CHENG,Yu-chen ZHANG,Cui FENG,Li-shi REN,Jian-jun LI,Yu-guang DU. Expression of Chitinase from Trichoderma reesei and Analysis the Composition and Structure of its Hydrolysates[J]. China Biotechnology, 2018, 38(10): 30-37.
[12] FENG Xue, GAO Xiang, NIU Chun-qing, LIU Yan. Construction of Pichia pastoris Expression Vector of Codon Optimized αB-crystallin Gene and Expression Optimization[J]. China Biotechnology, 2017, 37(7): 42-47.
[13] ZHAN Chun-jun, LI Xiang, LIU Guo-qiang, LIU Xiu-xia, YANG Yan-kun, BAI Zhong-hu. Identification of Glycerol Transporter in Pichia pastoris and Function Research[J]. China Biotechnology, 2017, 37(7): 48-55.
[14] YANG Xu, HUANG Wei-wei, YAO Yu-feng, LIU Cun-bao, SUN Wen-jia, BAI Hong-mei, MA Yan-bing. Impact Factors on the Expression of Recombinant Human Papillomavirus 16 L1 Protein in Pichia pastoris[J]. China Biotechnology, 2017, 37(10): 1-7.
[15] CHEN Long-guan, QIN Jin-hong, HUANG Yun-na, MAI Jun-xin, XIE Qiu-ling. Optimized Signal Peptides Sequences for the Development of High Expressing McAbs[J]. China Biotechnology, 2016, 36(3): 77-81.