Size-dependent ability of AtaA to immobilize cells in Acinetobacter sp. Tol 5.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
09 09 2024
Historique:
received: 27 06 2024
accepted: 31 08 2024
medline: 10 9 2024
pubmed: 10 9 2024
entrez: 9 9 2024
Statut: epublish

Résumé

Microbial cells serve as efficient and environmentally friendly biocatalysts, but their stability and reusability in practical applications must often be improved through immobilization. Acinetobacter sp. Tol 5 shows high adhesiveness to materials due to its large cell surface protein AtaA, which consists of 3630 amino acids (aa). Previously, we developed a method for immobilizing bacteria using AtaA. Herein, we investigated the cell immobilization ability of in-frame deletion (IFD) mutants of AtaA with different sizes in Tol 5. Mini-AtaA, which consists of 775 aa and is functional in Escherichia coli, was produced and present on the cell surface; however, mini-AtaA showed no immobilization ability in Tol 5. A cell immobilization assay was performed with cells expressing 16 IFD mutants of AtaA with different sizes, revealing that a length of at least 1417 aa was required for the sufficient immobilization of Tol 5 cells; thus, the minimum length needed to achieve the adhesive function of AtaA varies among bacterial species. The constructed mutant library of AtaA ranging from 3630 to 775 aa will allow researchers to quickly and easily explore the optimal size of AtaA, even for bacteria newly introduced to AtaA.

Identifiants

pubmed: 39251675
doi: 10.1038/s41598-024-71920-3
pii: 10.1038/s41598-024-71920-3
doi:

Substances chimiques

Bacterial Proteins 0
Membrane Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

21039

Informations de copyright

© 2024. The Author(s).

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Auteurs

Shogo Yoshimoto (S)

Department of Biomolecular Engineering, Graduate School of Engineering, Nagoya University, Nagoya, Aichi, 464-8603, Japan.

Sota Aoki (S)

Department of Biomolecular Engineering, Graduate School of Engineering, Nagoya University, Nagoya, Aichi, 464-8603, Japan.

Masahito Ishikawa (M)

Department of Frontier Bioscience, Faculty of Bioscience, Nagahama Institute of Bio-Science and Technology, Nagahama, Shiga, 526-0829, Japan.

Atsuo Suzuki (A)

Department of Biomolecular Engineering, Graduate School of Engineering, Nagoya University, Nagoya, Aichi, 464-8603, Japan.

Katsutoshi Hori (K)

Department of Biomolecular Engineering, Graduate School of Engineering, Nagoya University, Nagoya, Aichi, 464-8603, Japan. khori@chembio.nagoya-u.ac.jp.

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