SwePub
Sök i LIBRIS databas

  Extended search

L773:1046 5928 OR L773:1096 0279
 

Search: L773:1046 5928 OR L773:1096 0279 > (2020-2024) > Highly secretory ex...

Highly secretory expression of recombinant cowpea chlorotic mottle virus capsid proteins in Pichia pastoris and in-vitro encapsulation of ruthenium nanoparticles for catalysis

Zhu, Jie (author)
Changzhou Univ, Natl Local Joint Engn Res Ctr Biomass Refining &, Changzhou 213164, Peoples R China
Yang, Kun (author)
Changzhou Univ, Natl Local Joint Engn Res Ctr Biomass Refining &, Changzhou 213164, Peoples R China
Liu, Aijie (author)
Uppsala universitet,Fysikalisk kemi,Univ Twente, MESA Inst Nanotechnol, Dept Biomol Nanotechnol, NL-7500 AE Enschede, Netherlands
show more...
Lu, Xiaoxue (author)
Changzhou Univ, Natl Local Joint Engn Res Ctr Biomass Refining &, Changzhou 213164, Peoples R China
Yang, Linsong (author)
Changzhou Univ, Natl Local Joint Engn Res Ctr Biomass Refining &, Changzhou 213164, Peoples R China
Zhao, Qinghuan (author)
Changzhou Univ, Natl Local Joint Engn Res Ctr Biomass Refining &, Changzhou 213164, Peoples R China; Suzhou BioTOP Tech Serv Co Ltd, Suzhou Ind Pk, Suzhou 215123, Peoples R China
show less...
 (creator_code:org_t)
Elsevier BV, 2020
2020
English.
In: Protein Expression and Purification. - : Elsevier BV. - 1046-5928 .- 1096-0279. ; 174
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • The applications of viral protein cages have expanded rapidly into the fields of bionanotechnology and materials science. However, the low-cost production of viral capsid proteins (CPs) on a large scale is always a challenge. Herein, we develop a highly efficient expression system by constructing recombinant Pichia pastoris cells as a “factory” for the secretion of soluble cowpea chlorotic mottle virus (CCMV) CPs. Under optimal induction conditions (0.9 mg/mL of methanol concentration at 30 °C for 96 h), a high yield of approximately 95 mg/L of CCMV CPs was harvested from the fermentation supernatant with CPs purity >90%, which has significantly simplified the rest of the purification process. The resultant CPs are employed to encapsulate Ruthenium (Ru) nanoparticles (NPs) via in-vitro self-assembly to prepare hybrid nanocatalyst, i.e. Ru@virus-like particles (VLPs). The catalytic activity over Ru@VLPs was evaluated by reducing 4-nitrophenol (4-NP) to 4-aminophenol (4-AP). The results indicate that, with the protection of protein cages, Ru NPs were highly stabilized during the catalytic reaction. This results in enhanced catalytic activity (reaction rate constant k = 0.14 min−1) in comparison with unsupported citrate-stabilized Ru NPs (Ru-CA) (k = 0.08 min−1). Additionally, comparatively lower activation energy over Ru@VLPs (approximately 32 kJ/mol) than that over Ru-CA (approximately 39 kJ/mol) could be attributed to the synergistic effect between Ru NPs and some functional groups such as amino groups (–NH2) on CPs that weakened the activation barrier of 4-NP reduction. Therefore, enhanced activity and decreased activation energy over Ru@VLPs demonstrated the superiority of Ru@VLPs to unsupported Ru-CA.

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

Pichiapastoris
Cowpeachloroticmottlevirus
Secretion
Virus-likeparticles
Hybridnanocatalyst
4-Nitrophenolreduction

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

To the university's database

Find more in SwePub

By the author/editor
Zhu, Jie
Yang, Kun
Liu, Aijie
Lu, Xiaoxue
Yang, Linsong
Zhao, Qinghuan
About the subject
NATURAL SCIENCES
NATURAL SCIENCES
and Biological Scien ...
and Biochemistry and ...
Articles in the publication
Protein Expressi ...
By the university
Uppsala University

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view