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CAZyChip: dynamic assessment of exploration of glycoside hydrolases in microbial ecosystems
被引:24
作者:
Abot, Anne
[1
,2
,3
]
Arnal, Gregory
[1
,2
,3
]
Auer, Lucas
[1
,2
,3
]
Lazuka, Adele
[1
,2
,3
]
Labourdette, Delphine
[1
,2
,3
]
Lamarre, Sophie
[1
,2
,3
]
Trouilh, Lidwine
[1
,2
,3
]
Laville, Elisabeth
[1
,2
,3
]
Lombard, Vincent
[4
,5
,6
]
Potocki-Veronese, Gabrielle
[1
,2
,3
]
Henrissat, Bernard
[4
,5
,6
,7
]
O'Donohue, Michael
[1
,2
,3
]
Hernandez-Raquet, Guillermina
[1
,2
,3
]
Dumon, Claire
[1
,2
,3
]
Leberre, Veronique Anton
[1
,2
,3
,8
]
机构:
[1] Univ Toulouse, INSA, UPS, INP,LISBP, 135 Ave Rangueil, F-31077 Toulouse, France
[2] INRA, Ingn Syst Biol & Proc UMR792, F-31400 Toulouse, France
[3] CNRS, UMR5504, F-31400 Toulouse, France
[4] CNRS, UMR 7257, F-13288 Marseille, France
[5] Aix Marseille Univ, Architecture & Fonct Macromol Biol, F-13288 Marseille, France
[6] USC 1408 AFMB, INRA, F-13288 Marseille, France
[7] King Abdulaziz Univ, Dept Biol Sci, Jeddah, Saudi Arabia
[8] INRA 792, CNRS 5504, UMR INSA, LISBP, INSA Batiment Bio 5,135 Ave Rangueil, F-31077 Toulouse 4, France
来源:
关键词:
CAZymes detection;
Glycoside hydrolase;
Microarray;
Microbial functional diversity;
Plant cell wall degradation;
Transcriptomic analysis;
PLANT-CELL WALL;
CARBOHYDRATE-ACTIVE ENZYMES;
HIGH-THROUGHPUT TOOL;
HUMAN GUT MICROBIOME;
TRICHODERMA-REESEI;
HIGHLY EFFICIENT;
DNA MICROARRAY;
EXPRESSION;
BIOMASS;
IDENTIFICATION;
D O I:
10.1186/s12864-016-2988-4
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Background: Microorganisms constitute a reservoir of enzymes involved in environmental carbon cycling and degradation of plant polysaccharides through their production of a vast variety of Glycoside Hydrolases (GH). The CAZyChip was developed to allow a rapid characterization at transcriptomic level of these GHs and to identify enzymes acting on hydrolysis of polysaccharides or glycans. Results: This DNA biochip contains the signature of 55,220 bacterial GHs available in the CAZy database. Probes were designed using two softwares, and microarrays were directly synthesized using the in situ ink jet technology. CAZyChip specificity and reproducibility was validated by hybridization of known GHs RNA extracted from recombinant E. coli strains, which were previously identified by a functional metagenomic approach. The GHs arsenal was also studied in bioprocess conditions using rumen derived microbiota. Conclusions: The CAZyChip appears to be a user friendly tool for profiling the expression of a large variety of GHs. It can be used to study temporal variations of functional diversity, thereby facilitating the identification of new efficient candidates for enzymatic conversions from various ecosystems.
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