Cooperation of hydrolysis modes among xylanases reveals the mechanism of hemicellulose hydrolysis by Penicillium chrysogenum P33

Abstract Background Xylanases randomly cleave the internal β-1,4-glycosidic bonds in the xylan backbone and are grouped into different families in the carbohydrate-active enzyme (CAZy) database. Although multiple xylanases are detected in single strains of many filamentous fungi, no study has been r...

Full description

Bibliographic Details
Main Authors: Yi Yang, Jinshui Yang, Ruonan Wang, Jiawen Liu, Yu Zhang, Liang Liu, Fengqin Wang, Hongli Yuan
Format: Article
Language:English
Published: BMC 2019-09-01
Series:Microbial Cell Factories
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12934-019-1212-z
id doaj-ecff40dc419c47609ff419d4bc63dcb0
record_format Article
spelling doaj-ecff40dc419c47609ff419d4bc63dcb02020-11-25T03:27:53ZengBMCMicrobial Cell Factories1475-28592019-09-0118111310.1186/s12934-019-1212-zCooperation of hydrolysis modes among xylanases reveals the mechanism of hemicellulose hydrolysis by Penicillium chrysogenum P33Yi Yang0Jinshui Yang1Ruonan Wang2Jiawen Liu3Yu Zhang4Liang Liu5Fengqin Wang6Hongli Yuan7State Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural UniversityState Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural UniversityState Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural UniversityState Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural UniversityState Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural UniversityState Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural UniversityCollege of Life Science, Henan Agricultural UniversityState Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural UniversityAbstract Background Xylanases randomly cleave the internal β-1,4-glycosidic bonds in the xylan backbone and are grouped into different families in the carbohydrate-active enzyme (CAZy) database. Although multiple xylanases are detected in single strains of many filamentous fungi, no study has been reported on the composition, synergistic effect, and mode of action in a complete set of xylanases secreted by the same microorganism. Results All three xylanases secreted by Penicillium chrysogenum P33 were expressed and characterized. The enzymes Xyl1 and Xyl3 belong to the GH10 family and Xyl3 contains a CBM1 domain at its C-terminal, whereas Xyl2 belongs to the GH11 family. The optimal temperature/pH values were 35 °C/6.0, 50 °C/5.0 and 55 °C/6.0 for Xyl1, Xyl2, and Xyl3, respectively. The three xylanases exhibited synergistic effects, with the maximum synergy observed between Xyl3 and Xyl2, which are from different families. The synergy between xylanases could also improve the hydrolysis of cellulase (C), with the maximum amount of reducing sugars (5.68 mg/mL) observed using the combination of C + Xyl2 + Xyl3. Although the enzymatic activity of Xyl1 toward xylan was low, it was shown to be capable of hydrolyzing xylooligosaccharides into xylose. Xyl2 was shown to hydrolyze xylan to long-chain xylooligosaccharides, whereas Xyl3 hydrolyzed xylan to xylooligosaccharides with a lower degree of polymerization. Conclusions Synergistic effect exists among different xylanases, and it was higher between xylanases from different families. The cooperation of hydrolysis modes comprised the primary mechanism for the observed synergy between different xylanases. This study demonstrated, for the first time, that the hydrolysates of GH11 xylanases can be further hydrolyzed by GH10 xylanases, but not vice versa.http://link.springer.com/article/10.1186/s12934-019-1212-zPenicillium chrysogenumXylanaseEnzymatic hydrolysisCooperationHydrolysis mode
collection DOAJ
language English
format Article
sources DOAJ
author Yi Yang
Jinshui Yang
Ruonan Wang
Jiawen Liu
Yu Zhang
Liang Liu
Fengqin Wang
Hongli Yuan
spellingShingle Yi Yang
Jinshui Yang
Ruonan Wang
Jiawen Liu
Yu Zhang
Liang Liu
Fengqin Wang
Hongli Yuan
Cooperation of hydrolysis modes among xylanases reveals the mechanism of hemicellulose hydrolysis by Penicillium chrysogenum P33
Microbial Cell Factories
Penicillium chrysogenum
Xylanase
Enzymatic hydrolysis
Cooperation
Hydrolysis mode
author_facet Yi Yang
Jinshui Yang
Ruonan Wang
Jiawen Liu
Yu Zhang
Liang Liu
Fengqin Wang
Hongli Yuan
author_sort Yi Yang
title Cooperation of hydrolysis modes among xylanases reveals the mechanism of hemicellulose hydrolysis by Penicillium chrysogenum P33
title_short Cooperation of hydrolysis modes among xylanases reveals the mechanism of hemicellulose hydrolysis by Penicillium chrysogenum P33
title_full Cooperation of hydrolysis modes among xylanases reveals the mechanism of hemicellulose hydrolysis by Penicillium chrysogenum P33
title_fullStr Cooperation of hydrolysis modes among xylanases reveals the mechanism of hemicellulose hydrolysis by Penicillium chrysogenum P33
title_full_unstemmed Cooperation of hydrolysis modes among xylanases reveals the mechanism of hemicellulose hydrolysis by Penicillium chrysogenum P33
title_sort cooperation of hydrolysis modes among xylanases reveals the mechanism of hemicellulose hydrolysis by penicillium chrysogenum p33
publisher BMC
series Microbial Cell Factories
issn 1475-2859
publishDate 2019-09-01
description Abstract Background Xylanases randomly cleave the internal β-1,4-glycosidic bonds in the xylan backbone and are grouped into different families in the carbohydrate-active enzyme (CAZy) database. Although multiple xylanases are detected in single strains of many filamentous fungi, no study has been reported on the composition, synergistic effect, and mode of action in a complete set of xylanases secreted by the same microorganism. Results All three xylanases secreted by Penicillium chrysogenum P33 were expressed and characterized. The enzymes Xyl1 and Xyl3 belong to the GH10 family and Xyl3 contains a CBM1 domain at its C-terminal, whereas Xyl2 belongs to the GH11 family. The optimal temperature/pH values were 35 °C/6.0, 50 °C/5.0 and 55 °C/6.0 for Xyl1, Xyl2, and Xyl3, respectively. The three xylanases exhibited synergistic effects, with the maximum synergy observed between Xyl3 and Xyl2, which are from different families. The synergy between xylanases could also improve the hydrolysis of cellulase (C), with the maximum amount of reducing sugars (5.68 mg/mL) observed using the combination of C + Xyl2 + Xyl3. Although the enzymatic activity of Xyl1 toward xylan was low, it was shown to be capable of hydrolyzing xylooligosaccharides into xylose. Xyl2 was shown to hydrolyze xylan to long-chain xylooligosaccharides, whereas Xyl3 hydrolyzed xylan to xylooligosaccharides with a lower degree of polymerization. Conclusions Synergistic effect exists among different xylanases, and it was higher between xylanases from different families. The cooperation of hydrolysis modes comprised the primary mechanism for the observed synergy between different xylanases. This study demonstrated, for the first time, that the hydrolysates of GH11 xylanases can be further hydrolyzed by GH10 xylanases, but not vice versa.
topic Penicillium chrysogenum
Xylanase
Enzymatic hydrolysis
Cooperation
Hydrolysis mode
url http://link.springer.com/article/10.1186/s12934-019-1212-z
work_keys_str_mv AT yiyang cooperationofhydrolysismodesamongxylanasesrevealsthemechanismofhemicellulosehydrolysisbypenicilliumchrysogenump33
AT jinshuiyang cooperationofhydrolysismodesamongxylanasesrevealsthemechanismofhemicellulosehydrolysisbypenicilliumchrysogenump33
AT ruonanwang cooperationofhydrolysismodesamongxylanasesrevealsthemechanismofhemicellulosehydrolysisbypenicilliumchrysogenump33
AT jiawenliu cooperationofhydrolysismodesamongxylanasesrevealsthemechanismofhemicellulosehydrolysisbypenicilliumchrysogenump33
AT yuzhang cooperationofhydrolysismodesamongxylanasesrevealsthemechanismofhemicellulosehydrolysisbypenicilliumchrysogenump33
AT liangliu cooperationofhydrolysismodesamongxylanasesrevealsthemechanismofhemicellulosehydrolysisbypenicilliumchrysogenump33
AT fengqinwang cooperationofhydrolysismodesamongxylanasesrevealsthemechanismofhemicellulosehydrolysisbypenicilliumchrysogenump33
AT hongliyuan cooperationofhydrolysismodesamongxylanasesrevealsthemechanismofhemicellulosehydrolysisbypenicilliumchrysogenump33
_version_ 1724586606439956480