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High-Level Expression and Biochemical Properties of A Thermo-Alkaline Pectate Lyase From Bacillus sp. RN1 in Pichia pastoris With Potential in Ramie Degumming
Pectate lyases play an essential role in textiles, animal feed, and oil extraction industries. Pichia pastoris can be an ideal platform for pectate lyases production, and BspPel (a thermo-alkaline pectate lyase from Bacillus sp. RN1) was overexpressed by combined strategies, reaching 1859 U/mL in a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396651/ https://www.ncbi.nlm.nih.gov/pubmed/32850721 http://dx.doi.org/10.3389/fbioe.2020.00850 |
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author | Zheng, Xueyun Zhang, Yimin Liu, Xiaoxiao Li, Cheng Lin, Ying Liang, Shuli |
author_facet | Zheng, Xueyun Zhang, Yimin Liu, Xiaoxiao Li, Cheng Lin, Ying Liang, Shuli |
author_sort | Zheng, Xueyun |
collection | PubMed |
description | Pectate lyases play an essential role in textiles, animal feed, and oil extraction industries. Pichia pastoris can be an ideal platform for pectate lyases production, and BspPel (a thermo-alkaline pectate lyase from Bacillus sp. RN1) was overexpressed by combined strategies, reaching 1859 U/mL in a 50 L fermentator. It displayed the highest activity at 80°C, and maintained more than 60% of the activity between 30 and 70°C for 1 h. It showed an optimal pH of 10.0, and exhibited remarkable stability over a wider pH range (3.0-11.0), retaining more than 80.0% of enzyme activity for 4 h. The K(m) and k(cat) of BspPel on PGA (polygalacturonic acid) was 2.19 g L(–1) and 116.1 s(–1), respectively. The activity was significantly enhanced by Ca(2+), Mn(2+), and Cu(2+), and a slight increase was observed with the addition of Ba(2+) and Mg(2+). Scanning electron microscope was used to show the degumming efficiency of BspPel on ramie fibers. The loss weight was 9.2% when treated with crude enzyme supernatant and 20.8% when treated with the enzyme-chemical method, which was higher than the 14.2% weight loss in the positive control treated with 0.5% (w/v) NaOH alone. In conclusion, BspPel could be a good candidate for the ramie degumming industry. |
format | Online Article Text |
id | pubmed-7396651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73966512020-08-25 High-Level Expression and Biochemical Properties of A Thermo-Alkaline Pectate Lyase From Bacillus sp. RN1 in Pichia pastoris With Potential in Ramie Degumming Zheng, Xueyun Zhang, Yimin Liu, Xiaoxiao Li, Cheng Lin, Ying Liang, Shuli Front Bioeng Biotechnol Bioengineering and Biotechnology Pectate lyases play an essential role in textiles, animal feed, and oil extraction industries. Pichia pastoris can be an ideal platform for pectate lyases production, and BspPel (a thermo-alkaline pectate lyase from Bacillus sp. RN1) was overexpressed by combined strategies, reaching 1859 U/mL in a 50 L fermentator. It displayed the highest activity at 80°C, and maintained more than 60% of the activity between 30 and 70°C for 1 h. It showed an optimal pH of 10.0, and exhibited remarkable stability over a wider pH range (3.0-11.0), retaining more than 80.0% of enzyme activity for 4 h. The K(m) and k(cat) of BspPel on PGA (polygalacturonic acid) was 2.19 g L(–1) and 116.1 s(–1), respectively. The activity was significantly enhanced by Ca(2+), Mn(2+), and Cu(2+), and a slight increase was observed with the addition of Ba(2+) and Mg(2+). Scanning electron microscope was used to show the degumming efficiency of BspPel on ramie fibers. The loss weight was 9.2% when treated with crude enzyme supernatant and 20.8% when treated with the enzyme-chemical method, which was higher than the 14.2% weight loss in the positive control treated with 0.5% (w/v) NaOH alone. In conclusion, BspPel could be a good candidate for the ramie degumming industry. Frontiers Media S.A. 2020-07-24 /pmc/articles/PMC7396651/ /pubmed/32850721 http://dx.doi.org/10.3389/fbioe.2020.00850 Text en Copyright © 2020 Zheng, Zhang, Liu, Li, Lin and Liang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Zheng, Xueyun Zhang, Yimin Liu, Xiaoxiao Li, Cheng Lin, Ying Liang, Shuli High-Level Expression and Biochemical Properties of A Thermo-Alkaline Pectate Lyase From Bacillus sp. RN1 in Pichia pastoris With Potential in Ramie Degumming |
title | High-Level Expression and Biochemical Properties of A Thermo-Alkaline Pectate Lyase From Bacillus sp. RN1 in Pichia pastoris With Potential in Ramie Degumming |
title_full | High-Level Expression and Biochemical Properties of A Thermo-Alkaline Pectate Lyase From Bacillus sp. RN1 in Pichia pastoris With Potential in Ramie Degumming |
title_fullStr | High-Level Expression and Biochemical Properties of A Thermo-Alkaline Pectate Lyase From Bacillus sp. RN1 in Pichia pastoris With Potential in Ramie Degumming |
title_full_unstemmed | High-Level Expression and Biochemical Properties of A Thermo-Alkaline Pectate Lyase From Bacillus sp. RN1 in Pichia pastoris With Potential in Ramie Degumming |
title_short | High-Level Expression and Biochemical Properties of A Thermo-Alkaline Pectate Lyase From Bacillus sp. RN1 in Pichia pastoris With Potential in Ramie Degumming |
title_sort | high-level expression and biochemical properties of a thermo-alkaline pectate lyase from bacillus sp. rn1 in pichia pastoris with potential in ramie degumming |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396651/ https://www.ncbi.nlm.nih.gov/pubmed/32850721 http://dx.doi.org/10.3389/fbioe.2020.00850 |
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