Combine strategy of treated activated charcoal and cell surface protein curli induction for enhanced performance in Escherichia coli immobilization

[Display omitted] •NaOH treatment increased surface area, pore volume and macropore size.•NaOH-treated activated charcoal increased cell adsorption by >120 %.•Production of curli enhanced the adsorption of E. coli by 50 %.•NaOH treatment and curli induction together increased overall cell adsorpt...

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Veröffentlicht in:Process biochemistry (1991) 2021-11, Vol.110, p.26-36
Hauptverfasser: Pachelles, Samson, Fuzi, Siti Fatimah Zaharah Mohamad, Man, Rohaida Che, Abdullah, Azian Azamimi, Illias, Rosli Md
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container_end_page 36
container_issue
container_start_page 26
container_title Process biochemistry (1991)
container_volume 110
creator Pachelles, Samson
Fuzi, Siti Fatimah Zaharah Mohamad
Man, Rohaida Che
Abdullah, Azian Azamimi
Illias, Rosli Md
description [Display omitted] •NaOH treatment increased surface area, pore volume and macropore size.•NaOH-treated activated charcoal increased cell adsorption by >120 %.•Production of curli enhanced the adsorption of E. coli by 50 %.•NaOH treatment and curli induction together increased overall cell adsorption by >160 %. Immobilization of Escherichia coli (E. coli) on commercial activated charcoal was enhanced by mild chemical treatment coupled with curli production from E. coli. The chemical used to treat the activated charcoal were sodium hydroxide, hydrochloric acid, ammonium hydroxide, and acetic acid while nickel (II) chloride was used to promote the production of curli. Characteristics of the activated charcoal before and after chemical treatments were analyzed including its surface properties, pore size, and crystalline structure. The immobilization of E. coli was enhanced greatly after sodium hydroxide treatment which gave rise to more than 120 % cell immobilized compared to the untreated activated charcoal which was mainly attributed to the larger size of macropore, surface area, and pore volume. Curli were produced by the induction of nickel (II) chloride and further enhanced the cell immobilization by at least 50 %. Overall, the combine strategy enhanced cell immobilization by more than 160 %. The resulting biocatalyst from the enhanced cell immobilization managed to be reused up to 10 cycles for the enzyme cyclodextrin glucanotransferase expression while retaining up to 60 % of the enzyme’s initial activity.
doi_str_mv 10.1016/j.procbio.2021.06.012
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Immobilization of Escherichia coli (E. coli) on commercial activated charcoal was enhanced by mild chemical treatment coupled with curli production from E. coli. The chemical used to treat the activated charcoal were sodium hydroxide, hydrochloric acid, ammonium hydroxide, and acetic acid while nickel (II) chloride was used to promote the production of curli. Characteristics of the activated charcoal before and after chemical treatments were analyzed including its surface properties, pore size, and crystalline structure. The immobilization of E. coli was enhanced greatly after sodium hydroxide treatment which gave rise to more than 120 % cell immobilized compared to the untreated activated charcoal which was mainly attributed to the larger size of macropore, surface area, and pore volume. Curli were produced by the induction of nickel (II) chloride and further enhanced the cell immobilization by at least 50 %. 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source ScienceDirect Journals (5 years ago - present)
subjects Acetic acid
Activated carbon
Activated charcoal
Ammonium
Ammonium hydroxide
Biocatalyst
Caustic soda
Cell immobilization
Cell surface
Charcoal
Chemical treatment
Chlorides
Curli
Cyclodextrin
Cyclodextrins
E coli
Enzymes
Escherichia coli
Hydrochloric acid
Immobilization
Nickel
Pore size
Sodium hydroxide
Surface properties
title Combine strategy of treated activated charcoal and cell surface protein curli induction for enhanced performance in Escherichia coli immobilization
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