Literature DB >> 34272577

Improving the functionality of surface-engineered yeast cells by altering the cell wall morphology of the host strain.

Kentaro Inokuma1, Yuki Kitada1, Takahiro Bamba1, Yuma Kobayashi1, Takahiro Yukawa1, Riaan den Haan2, Willem Heber van Zyl3, Akihiko Kondo1,4,5, Tomohisa Hasunuma6,7.   

Abstract

The expression of functional proteins on the cell surface using glycosylphosphatidylinositol (GPI)-anchoring technology is a promising approach for constructing yeast cells with special functions. The functionality of surface-engineered yeast strains strongly depends on the amount of functional proteins displayed on their cell surface. On the other hand, since the yeast cell wall space is finite, heterologous protein carrying capacity of the cell wall is limited. Here, we report the effect of CCW12 and CCW14 knockout, which encode major nonenzymatic GPI-anchored cell wall proteins (GPI-CWPs) involved in the cell wall organization, on the heterologous protein carrying capacity of yeast cell wall. Aspergillus aculeatus β-glucosidase (BGL) was used as a reporter to evaluate the protein carrying capacity in Saccharomyces cerevisiae. No significant difference in the amount of cell wall-associated BGL and cell-surface BGL activity was observed between CCW12 and CCW14 knockout strains and their control strain. In contrast, in the CCW12 and CCW14 co-knockout strains, the amount of cell wall-associated BGL and its activity were approximately 1.4-fold higher than those of the control strain and CCW12 or CCW14 knockout strains. Electron microscopic observation revealed that the total cell wall thickness of the CCW12 and CCW14 co-knockout strains was increased compared to the parental strain, suggesting a potential increase in heterologous protein carrying capacity of the cell wall. These results indicate that the CCW12 and CCW14 co-knockout strains are a promising host for the construction of highly functional recombinant yeast strains using cell-surface display technology. KEY POINTS: • CCW12 and/or CCW14 of a BGL-displaying S. cerevisiae strain were knocked out. • CCW12 and CCW14 co-disruption improved the display efficiency of BGL. • The thickness of the yeast cell wall was increased upon CCW12 and CCW14 knockout.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Glycosylphosphatidylinositol-anchored cell wall protein; Saccharomyces cerevisiae; Yeast surface display; cell wall morphology

Year:  2021        PMID: 34272577     DOI: 10.1007/s00253-021-11440-6

Source DB:  PubMed          Journal:  Appl Microbiol Biotechnol        ISSN: 0175-7598            Impact factor:   4.813


  32 in total

1.  One-step transformation of yeast in stationary phase.

Authors:  D C Chen; B C Yang; T T Kuo
Journal:  Curr Genet       Date:  1992-01       Impact factor: 3.886

2.  A simple and immediate method for simultaneously evaluating expression level and plasmid maintenance in yeast.

Authors:  Jun Ishii; Keiko Izawa; Shizuka Matsumura; Kanako Wakamura; Takanori Tanino; Tsutomu Tanaka; Chiaki Ogino; Hideki Fukuda; Akihiko Kondo
Journal:  J Biochem       Date:  2009-02-23       Impact factor: 3.387

3.  Enhanced cell-surface display of a heterologous protein using SED1 anchoring system in SED1-disrupted Saccharomyces cerevisiae strain.

Authors:  Takahiro Bamba; Kentaro Inokuma; Tomohisa Hasunuma; Akihiko Kondo
Journal:  J Biosci Bioeng       Date:  2017-11-23       Impact factor: 2.894

4.  Efficient co-displaying and artificial ratio control of α-amylase and glucoamylase on the yeast cell surface by using combinations of different anchoring domains.

Authors:  Kentaro Inokuma; Takanobu Yoshida; Jun Ishii; Tomohisa Hasunuma; Akihiko Kondo
Journal:  Appl Microbiol Biotechnol       Date:  2014-11-30       Impact factor: 4.813

5.  Protein Engineering and Selection Using Yeast Surface Display.

Authors:  Alessandro Angelini; Tiffany F Chen; Seymour de Picciotto; Nicole J Yang; Alice Tzeng; Michael S Santos; James A Van Deventer; Michael W Traxlmayr; K Dane Wittrup
Journal:  Methods Mol Biol       Date:  2015

Review 6.  'Strengthening the fungal cell wall through chitin-glucan cross-links: effects on morphogenesis and cell integrity'.

Authors:  Javier Arroyo; Vladimír Farkaš; Ana Belén Sanz; Enrico Cabib
Journal:  Cell Microbiol       Date:  2016-06-16       Impact factor: 3.715

7.  Enhanced cell-surface display and secretory production of cellulolytic enzymes with Saccharomyces cerevisiae Sed1 signal peptide.

Authors:  Kentaro Inokuma; Takahiro Bamba; Jun Ishii; Yoichiro Ito; Tomohisa Hasunuma; Akihiko Kondo
Journal:  Biotechnol Bioeng       Date:  2016-06-03       Impact factor: 4.530

8.  Novel strategy for anchorage position control of GPI-attached proteins in the yeast cell wall using different GPI-anchoring domains.

Authors:  Kentaro Inokuma; Hiroki Kurono; Riaan den Haan; Willem Heber van Zyl; Tomohisa Hasunuma; Akihiko Kondo
Journal:  Metab Eng       Date:  2019-11-09       Impact factor: 9.783

9.  Enhancement of protein production via the strong DIT1 terminator and two RNA-binding proteins in Saccharomyces cerevisiae.

Authors:  Yoichiro Ito; Takao Kitagawa; Mamoru Yamanishi; Satoshi Katahira; Shingo Izawa; Kenji Irie; Makoto Furutani-Seiki; Takashi Matsuyama
Journal:  Sci Rep       Date:  2016-11-15       Impact factor: 4.379

10.  Efficient yeast cell-surface display of exo- and endo-cellulase using the SED1 anchoring region and its original promoter.

Authors:  Kentaro Inokuma; Tomohisa Hasunuma; Akihiko Kondo
Journal:  Biotechnol Biofuels       Date:  2014-01-14       Impact factor: 6.040

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  2 in total

1.  Protective effects of peptides on the cell wall structure of yeast under osmotic stress.

Authors:  Xiaofan Jin; Moutong Chen; Teodora Emilia Coldea; Huirong Yang; Haifeng Zhao
Journal:  Appl Microbiol Biotechnol       Date:  2022-10-03       Impact factor: 5.560

Review 2.  Yeast Surface Display System: Strategies for Improvement and Biotechnological Applications.

Authors:  Karla V Teymennet-Ramírez; Fernando Martínez-Morales; María R Trejo-Hernández
Journal:  Front Bioeng Biotechnol       Date:  2022-01-10
  2 in total

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