Innovative Bioprocess Strategies Combining Physiological Control and Strain Engineering of Pichia pastoris to Improve Recombinant Protein Production

被引:11
|
作者
Gasset, Arnau [1 ]
Garcia-Ortega, Xavier [1 ,2 ]
Garrigos-Martinez, Javier [1 ]
Valero, Francisco [1 ]
Montesinos-Segui, Jose Luis [1 ]
机构
[1] Univ Autonoma Barcelona, Sch Engn, Dept Chem Biol & Environm Engn, Bellaterra, Spain
[2] Univ Vic Univ Cent Catalunya, Fac Sci & Technol, Dept Biosci, QuBi Lab, Vic, Spain
关键词
GAP promoter; Pichia pastoris (Komagataella phaffii); physiological control; transcriptional analysis; recombinant gene dosage; respiratory quotient; hypoxia; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE PROMOTER; BIOREACTOR OPERATION; CANDIDA-RUGOSA; GENE DOSAGE; EXPRESSION; CULTIVATION; SECRETION;
D O I
10.3389/fbioe.2022.818434
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The combination of strain and bioprocess engineering strategies should be considered to obtain the highest levels of recombinant protein production (RPP) while assuring product quality and process reproducibility of heterologous products. In this work, two complementary approaches were investigated to improve bioprocess efficiency based on the yeast P. pastoris. Firstly, the performance of two Candida rugosa lipase 1 producer clones with different gene dosage under the regulation of the constitutive P-GAP were compared in chemostat cultures with different oxygen-limiting conditions. Secondly, hypoxic conditions in carbon-limited fed-batch cultures were applied by means of a physiological control based on the respiratory quotient (RQ). Stirring rate was selected to maintain RQ between 1.4 and 1.6, since it was found to be the most favorable in chemostat. As the major outcome, between 2-fold and 4-fold higher specific production rate (q(P)) values were observed when comparing multicopy clone (MCC) and single-copy clone (SCC), both in chemostat and fed-batch. Additionally, when applying oxygen limitation, between 1.5-fold and 3-fold higher q(P) values were obtained compared with normoxic conditions. Thus, notable increases of up to 9-fold in the production rates were reached. Furthermore, transcriptional analysis of certain key genes related to RPP and central carbon metabolism were performed. Results seem to indicate the presence of a limitation in post-transcriptional protein processing steps and a possible transcription attenuation of the target gene in the strains with high gene dosage. The entire approach, including both strain and bioprocess engineering, represents a relevant novelty involving physiological control in Pichia cell factory and is of crucial interest in bioprocess optimization, boosting RPP, allowing bioproducts to be economically competitive in the market, and helping develop the bioeconomy.
引用
收藏
页数:12
相关论文
共 50 条
  • [1] Bioprocess engineering aspects of heterologous protein production in Pichia pastoris: A review
    Potvin, Gabriel
    Ahmad, Ayla
    Zhang, Zisheng
    BIOCHEMICAL ENGINEERING JOURNAL, 2012, 64 : 91 - 105
  • [2] Strategies in Pichia pastoris fermentation for recombinant protein mass production
    Tang, Shuiquan
    Hastie, Michele
    Carriere, Nick
    Zhang, Zisheng
    JOURNAL OF BIOTECHNOLOGY, 2008, 136 : S284 - S285
  • [3] Engineering protein translocation pathway to improve recombinant proteins in Pichia pastoris
    Wang, Shengyan
    Dai, Huijia
    Tang, Qingling
    Yu, Yujing
    Xie, Yaying
    Wang, Tao
    Huang, Yide
    CURRENT RESEARCH IN BIOTECHNOLOGY, 2024, 7
  • [4] Production of recombinant protein in Pichia pastoris by fermentation
    Berend Tolner
    Lisa Smith
    Richard H J Begent
    Kerry A Chester
    Nature Protocols, 2006, 1 : 1006 - 1021
  • [5] Production of recombinant protein in Pichia pastoris by fermentation
    Tolner, Berend
    Smith, Lisa
    Begent, Richard H. J.
    Chester, Kerry A.
    NATURE PROTOCOLS, 2006, 1 (02) : 1006 - 1021
  • [6] Model-based specific growth rate control for Pichia pastoris to improve recombinant protein production
    Ren, HT
    Yuan, JQ
    JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2005, 80 (11) : 1268 - 1272
  • [7] Bioprocess performance analysis of novel methanol-independent promoters for recombinant protein production with Pichia pastoris
    Javier Garrigós-Martínez
    Kiira Vuoristo
    Miguel Angel Nieto-Taype
    Juha Tähtiharju
    Jaana Uusitalo
    Pauliina Tukiainen
    Christian Schmid
    Ilya Tolstorukov
    Knut Madden
    Merja Penttilä
    José Luis Montesinos-Seguí
    Francisco Valero
    Anton Glieder
    Xavier Garcia-Ortega
    Microbial Cell Factories, 20
  • [8] Bioprocess performance analysis of novel methanol-independent promoters for recombinant protein production with Pichia pastoris
    Garrigos-Martinez, Javier
    Vuoristo, Kiira
    Nieto-Taype, Miguel Angel
    Taehtiharju, Juha
    Uusitalo, Jaana
    Tukiainen, Pauliina
    Schmid, Christian
    Tolstorukov, Ilya
    Madden, Knut
    Penttila, Merja
    Montesinos-Segui, Jose Luis
    Valero, Francisco
    Glieder, Anton
    Garcia-Ortega, Xavier
    MICROBIAL CELL FACTORIES, 2021, 20 (01)
  • [9] Recombinant protein production in Pichia pastoris: from transcriptionally redesigned strains to bioprocess optimization and metabolic modelling
    Ergun, Burcu Gundus
    Berrios, Julio
    Binay, Baris
    Fickers, Patrick
    FEMS YEAST RESEARCH, 2021, 21 (07)
  • [10] Quantitative comparison of dynamic physiological feeding profiles for recombinant protein production with Pichia pastoris
    Oliver Spadiut
    Denes Zalai
    Christian Dietzsch
    Christoph Herwig
    Bioprocess and Biosystems Engineering, 2014, 37 : 1163 - 1172