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Rational re-design of Lactobacillus reuteri 121 inulosucrase for product chain length control

Fructooligosaccharides (FOSs) are well-known prebiotics that are widely used in the food, beverage and pharmaceutical industries. Inulosucrase (E.C. 2.4.1.9) can potentially be used to synthesise FOSs from sucrose. In this study, inulosucrase from Lactobacillus reuteri 121 was engineered by site-dir...

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Autores principales: Charoenwongpaiboon, Thanapon, Klaewkla, Methus, Chunsrivirot, Surasak, Wangpaiboon, Karan, Pichyangkura, Rath, Field, Robert A., Prousoontorn, Manchumas Hengsakul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064246/
https://www.ncbi.nlm.nih.gov/pubmed/35516339
http://dx.doi.org/10.1039/c9ra02137j
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author Charoenwongpaiboon, Thanapon
Klaewkla, Methus
Chunsrivirot, Surasak
Wangpaiboon, Karan
Pichyangkura, Rath
Field, Robert A.
Prousoontorn, Manchumas Hengsakul
author_facet Charoenwongpaiboon, Thanapon
Klaewkla, Methus
Chunsrivirot, Surasak
Wangpaiboon, Karan
Pichyangkura, Rath
Field, Robert A.
Prousoontorn, Manchumas Hengsakul
author_sort Charoenwongpaiboon, Thanapon
collection PubMed
description Fructooligosaccharides (FOSs) are well-known prebiotics that are widely used in the food, beverage and pharmaceutical industries. Inulosucrase (E.C. 2.4.1.9) can potentially be used to synthesise FOSs from sucrose. In this study, inulosucrase from Lactobacillus reuteri 121 was engineered by site-directed mutagenesis to change the FOS chain length. Three variants (R483F, R483Y and R483W) were designed, and their binding free energies with 1,1,1-kestopentaose (GF4) were calculated with the Rosetta software. R483F and R483Y were predicted to bind with GF4 better than the wild type, suggesting that these engineered enzymes should be able to effectively extend GF4 by one residue and produce a greater quantity of GF5 than the wild type. MALDI-TOF MS analysis showed that R483F, R483Y and R483W variants could synthesise shorter chain FOSs with a degree of polymerization (DP) up to 11, 10, and 10, respectively, while wild type produced longer FOSs and in polymeric form. Although the decrease in catalytic activity and the increase of hydrolysis/transglycosylation activity ratio was observed, the variants could effectively synthesise FOSs with the yield up to 73% of substrate. Quantitative analysis demonstrated that these variants produced a larger quantity of GF5 than wild type, which was in good agreement with the predicted binding free energy results. Our findings demonstrate the success of using aromatic amino acid residues, at position D418, to block the oligosaccharide binding track of inulosucrase in controlling product chain length.
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spelling pubmed-90642462022-05-04 Rational re-design of Lactobacillus reuteri 121 inulosucrase for product chain length control Charoenwongpaiboon, Thanapon Klaewkla, Methus Chunsrivirot, Surasak Wangpaiboon, Karan Pichyangkura, Rath Field, Robert A. Prousoontorn, Manchumas Hengsakul RSC Adv Chemistry Fructooligosaccharides (FOSs) are well-known prebiotics that are widely used in the food, beverage and pharmaceutical industries. Inulosucrase (E.C. 2.4.1.9) can potentially be used to synthesise FOSs from sucrose. In this study, inulosucrase from Lactobacillus reuteri 121 was engineered by site-directed mutagenesis to change the FOS chain length. Three variants (R483F, R483Y and R483W) were designed, and their binding free energies with 1,1,1-kestopentaose (GF4) were calculated with the Rosetta software. R483F and R483Y were predicted to bind with GF4 better than the wild type, suggesting that these engineered enzymes should be able to effectively extend GF4 by one residue and produce a greater quantity of GF5 than the wild type. MALDI-TOF MS analysis showed that R483F, R483Y and R483W variants could synthesise shorter chain FOSs with a degree of polymerization (DP) up to 11, 10, and 10, respectively, while wild type produced longer FOSs and in polymeric form. Although the decrease in catalytic activity and the increase of hydrolysis/transglycosylation activity ratio was observed, the variants could effectively synthesise FOSs with the yield up to 73% of substrate. Quantitative analysis demonstrated that these variants produced a larger quantity of GF5 than wild type, which was in good agreement with the predicted binding free energy results. Our findings demonstrate the success of using aromatic amino acid residues, at position D418, to block the oligosaccharide binding track of inulosucrase in controlling product chain length. The Royal Society of Chemistry 2019-05-14 /pmc/articles/PMC9064246/ /pubmed/35516339 http://dx.doi.org/10.1039/c9ra02137j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Charoenwongpaiboon, Thanapon
Klaewkla, Methus
Chunsrivirot, Surasak
Wangpaiboon, Karan
Pichyangkura, Rath
Field, Robert A.
Prousoontorn, Manchumas Hengsakul
Rational re-design of Lactobacillus reuteri 121 inulosucrase for product chain length control
title Rational re-design of Lactobacillus reuteri 121 inulosucrase for product chain length control
title_full Rational re-design of Lactobacillus reuteri 121 inulosucrase for product chain length control
title_fullStr Rational re-design of Lactobacillus reuteri 121 inulosucrase for product chain length control
title_full_unstemmed Rational re-design of Lactobacillus reuteri 121 inulosucrase for product chain length control
title_short Rational re-design of Lactobacillus reuteri 121 inulosucrase for product chain length control
title_sort rational re-design of lactobacillus reuteri 121 inulosucrase for product chain length control
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064246/
https://www.ncbi.nlm.nih.gov/pubmed/35516339
http://dx.doi.org/10.1039/c9ra02137j
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