In-Cell Engineering of Protein Crystals with Nanoporous Structures for Promoting Cascade Reactions

The development of solid biocatalysts has rapidly progressed for applications in nanomaterials. The immobilization of enzymes in solid materials is considered an alternative method for constructing traditional biocatalysts with high stability and efficiency to be reused. However, the design of solid...

Full description

Bibliographic Details
Main Authors: Tien K. Nguyen (10046576), Satoshi Abe (524075), Makoto Kasamatsu (10046579), Basudev Maity (2274049), Keitaro Yamashita (3712387), Kunio Hirata (480519), Mariko Kojima (10046582), Takafumi Ueno (541538)
Format: Other Non-Article Part of Journal/Newspaper
Language:unknown
Published: 2021
Subjects:
Online Access:https://doi.org/10.1021/acsanm.0c03129.s001
id ftsmithonian:oai:figshare.com:article/13656182
record_format openpolar
spelling ftsmithonian:oai:figshare.com:article/13656182 2023-05-15T13:59:57+02:00 In-Cell Engineering of Protein Crystals with Nanoporous Structures for Promoting Cascade Reactions Tien K. Nguyen (10046576) Satoshi Abe (524075) Makoto Kasamatsu (10046579) Basudev Maity (2274049) Keitaro Yamashita (3712387) Kunio Hirata (480519) Mariko Kojima (10046582) Takafumi Ueno (541538) 2021-01-28T00:00:00Z https://doi.org/10.1021/acsanm.0c03129.s001 unknown https://figshare.com/articles/journal_contribution/_i_In-Cell_i_Engineering_of_Protein_Crystals_with_Nanoporous_Structures_for_Promoting_Cascade_Reactions/13656182 doi:10.1021/acsanm.0c03129.s001 CC BY-NC 4.0 CC-BY-NC Biophysics Biochemistry Microbiology Molecular Biology Biotechnology Immunology Developmental Biology Infectious Diseases Space Science Chemical Sciences not elsewhere classified cascade reaction nanoporous materials reactivity enzyme Promoting Cascade Reactions Candida antarctica lipase B Lactobacillus kefir alcohol dehydro. in-cell protein crystals cytoplasmic polyhedrosis virus Text Journal contribution 2021 ftsmithonian https://doi.org/10.1021/acsanm.0c03129.s001 2021-02-03T08:52:06Z The development of solid biocatalysts has rapidly progressed for applications in nanomaterials. The immobilization of enzymes in solid materials is considered an alternative method for constructing traditional biocatalysts with high stability and efficiency to be reused. However, the design of solid scaffolds from nanoporous materials to immobilize multiple enzymes and improve catalytic reactivity remains challenging. In this study, the engineering of in-cell protein crystals is demonstrated to have the potential for immobilizing two enzymes that promote a cascade reaction. Polyhedra is known as an in-cell crystalline protein produced in insect cells by the infection of cytoplasmic polyhedrosis virus. We constructed the 38-residue-deletion mutant, which forms interlinked hollow nanocages with a diameter of 5 nm in the crystal. The mutant crystal can encapsulate Candida antarctica lipase B and Lactobacillus kefir alcohol dehydrogenase. The composite crystal significantly enhances the reactivity of the cascade reaction with 1.9-fold and 3.8-fold higher efficiency than that of the wild-type crystal and the mixture of the free enzymes, respectively. The higher reactivity is because of the substrate and intermediate efficiently diffusing through the extended channels designed within the nanoporous crystal. These results suggest the possibility of using polyhedrin crystals to design the nanoporous materials for developing further applications in bio-nanomaterial science. Other Non-Article Part of Journal/Newspaper Antarc* Antarctica Unknown
institution Open Polar
collection Unknown
op_collection_id ftsmithonian
language unknown
topic Biophysics
Biochemistry
Microbiology
Molecular Biology
Biotechnology
Immunology
Developmental Biology
Infectious Diseases
Space Science
Chemical Sciences not elsewhere classified
cascade reaction
nanoporous materials
reactivity
enzyme
Promoting Cascade Reactions
Candida antarctica lipase B
Lactobacillus kefir alcohol dehydro.
in-cell protein crystals
cytoplasmic polyhedrosis virus
spellingShingle Biophysics
Biochemistry
Microbiology
Molecular Biology
Biotechnology
Immunology
Developmental Biology
Infectious Diseases
Space Science
Chemical Sciences not elsewhere classified
cascade reaction
nanoporous materials
reactivity
enzyme
Promoting Cascade Reactions
Candida antarctica lipase B
Lactobacillus kefir alcohol dehydro.
in-cell protein crystals
cytoplasmic polyhedrosis virus
Tien K. Nguyen (10046576)
Satoshi Abe (524075)
Makoto Kasamatsu (10046579)
Basudev Maity (2274049)
Keitaro Yamashita (3712387)
Kunio Hirata (480519)
Mariko Kojima (10046582)
Takafumi Ueno (541538)
In-Cell Engineering of Protein Crystals with Nanoporous Structures for Promoting Cascade Reactions
topic_facet Biophysics
Biochemistry
Microbiology
Molecular Biology
Biotechnology
Immunology
Developmental Biology
Infectious Diseases
Space Science
Chemical Sciences not elsewhere classified
cascade reaction
nanoporous materials
reactivity
enzyme
Promoting Cascade Reactions
Candida antarctica lipase B
Lactobacillus kefir alcohol dehydro.
in-cell protein crystals
cytoplasmic polyhedrosis virus
description The development of solid biocatalysts has rapidly progressed for applications in nanomaterials. The immobilization of enzymes in solid materials is considered an alternative method for constructing traditional biocatalysts with high stability and efficiency to be reused. However, the design of solid scaffolds from nanoporous materials to immobilize multiple enzymes and improve catalytic reactivity remains challenging. In this study, the engineering of in-cell protein crystals is demonstrated to have the potential for immobilizing two enzymes that promote a cascade reaction. Polyhedra is known as an in-cell crystalline protein produced in insect cells by the infection of cytoplasmic polyhedrosis virus. We constructed the 38-residue-deletion mutant, which forms interlinked hollow nanocages with a diameter of 5 nm in the crystal. The mutant crystal can encapsulate Candida antarctica lipase B and Lactobacillus kefir alcohol dehydrogenase. The composite crystal significantly enhances the reactivity of the cascade reaction with 1.9-fold and 3.8-fold higher efficiency than that of the wild-type crystal and the mixture of the free enzymes, respectively. The higher reactivity is because of the substrate and intermediate efficiently diffusing through the extended channels designed within the nanoporous crystal. These results suggest the possibility of using polyhedrin crystals to design the nanoporous materials for developing further applications in bio-nanomaterial science.
format Other Non-Article Part of Journal/Newspaper
author Tien K. Nguyen (10046576)
Satoshi Abe (524075)
Makoto Kasamatsu (10046579)
Basudev Maity (2274049)
Keitaro Yamashita (3712387)
Kunio Hirata (480519)
Mariko Kojima (10046582)
Takafumi Ueno (541538)
author_facet Tien K. Nguyen (10046576)
Satoshi Abe (524075)
Makoto Kasamatsu (10046579)
Basudev Maity (2274049)
Keitaro Yamashita (3712387)
Kunio Hirata (480519)
Mariko Kojima (10046582)
Takafumi Ueno (541538)
author_sort Tien K. Nguyen (10046576)
title In-Cell Engineering of Protein Crystals with Nanoporous Structures for Promoting Cascade Reactions
title_short In-Cell Engineering of Protein Crystals with Nanoporous Structures for Promoting Cascade Reactions
title_full In-Cell Engineering of Protein Crystals with Nanoporous Structures for Promoting Cascade Reactions
title_fullStr In-Cell Engineering of Protein Crystals with Nanoporous Structures for Promoting Cascade Reactions
title_full_unstemmed In-Cell Engineering of Protein Crystals with Nanoporous Structures for Promoting Cascade Reactions
title_sort in-cell engineering of protein crystals with nanoporous structures for promoting cascade reactions
publishDate 2021
url https://doi.org/10.1021/acsanm.0c03129.s001
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_relation https://figshare.com/articles/journal_contribution/_i_In-Cell_i_Engineering_of_Protein_Crystals_with_Nanoporous_Structures_for_Promoting_Cascade_Reactions/13656182
doi:10.1021/acsanm.0c03129.s001
op_rights CC BY-NC 4.0
op_rightsnorm CC-BY-NC
op_doi https://doi.org/10.1021/acsanm.0c03129.s001
_version_ 1766268870459392000