Nicolas Terrapon

Dr. Nicolas Terrapon

orcid

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2016 in Cell
Verified
Journal Article
Closed access
MDMahesh Desai
Mahesh Desai
ASAnna M. Seekatz
Anna M. Seekatz
NKNicole M. Koropatkin
Nicole M. Koropatkin
NKNobuhiko Kamada
Nobuhiko Kamada
CHChristina A. Hickey
Christina A. Hickey
EMEric C. Martens
Eric C. Martens

29 November 2021 in Nucleic Acids Research
Verified
Journal Article
Open access
EDElodie Drula
Elodie Drula
MGMarie-Line Garron
Marie-Line Garron
SDSuzan Dogan
Suzan Dogan
VLVincent Lombard
Vincent Lombard
BHBernard Henrissat
Bernard Henrissat
NTNicolas Terrapon
Nicolas Terrapon
Thirty years have elapsed since the emergence of the classification of carbohydrate-active enzymes in sequence-based families that became the CAZy database over 20 years ago, freely available for browsing and download at www.cazy.org. In the era of large scale sequencing and high-throughput Biology, it is important to examine the position of this specialist database that is deeply rooted in human curation. The three primary tasks of the CAZy curators are (i) to maintain and update the family classification of this class of enzymes, (ii) to classify sequences newly released by GenBank and the Protein Data Bank and (iii) to capture and present functional information for each family. The CAZy website is updated once a month. Here we briefly summarize the increase in novel families and the annotations conducted during the last 8 years. We present several important changes that facilitate taxonomic navigation, and allow to download the entirety of the annotations. Most importantly we highlight the considerable amount of work that accompanies the analysis and report of biochemical data from the literature.

22 March 2017 in Nature
Verified
Journal Article
Open access
PDF file
DNDidier Ndeh
Didier Ndeh
ARArtur Rogowski
Artur Rogowski
ACAlan Cartmell
Alan Cartmell
ALAna S Luis
Ana S Luis
ABArnaud Baslé
Arnaud Baslé
HGHarry J. Gilbert
Harry J. Gilbert
The metabolism of carbohydrate polymers drives microbial diversity in the human gut microbiota. It is unclear, however, whether bacterial consortia or single organisms are required to depolymerize highly complex glycans. Here we show that the gut bacterium Bacteroides thetaiotaomicron uses the most structurally complex glycan known: the plant pectic polysaccharide rhamnogalacturonan-II, cleaving all but 1 of its 21 distinct glycosidic linkages. The deconstruction of rhamnogalacturonan-II side chains and backbone are coordinated to overcome steric constraints, and the degradation involves previously undiscovered enzyme families and catalytic activities. The degradation system informs revision of the current structural model of rhamnogalacturonan-II and highlights how individual gut bacteria orchestrate manifold enzymes to metabolize the most challenging glycan in the human diet.

19 March 2018 in Nature Biotechnology
Verified
Journal Article
Open access
PDF file
RSRekha Seshadri
Rekha Seshadri
SLSinead C Leahy
Sinead C Leahy
GAGraeme T Attwood
Graeme T Attwood
KTKoon Hoong Teh
Koon Hoong Teh
SLSuzanne C Lambie
Suzanne C Lambie
WKWilliam J Kelly
William J Kelly
Rumen microbiome biology gets a boost with the release of 410 high-quality reference genomes from the Hungate1000 project. Productivity of ruminant livestock depends on the rumen microbiota, which ferment indigestible plant polysaccharides into nutrients used for growth. Understanding the functions carried out by the rumen microbiota is important for reducing greenhouse gas production by ruminants and for developing biofuels from lignocellulose. We present 410 cultured bacteria and archaea, together with their reference genomes, representing every cultivated rumen-associated archaeal and bacterial family. We evaluate polysaccharide degradation, short-chain fatty acid production and methanogenesis pathways, and assign specific taxa to functions. A total of 336 organisms were present in available rumen metagenomic data sets, and 134 were present in human gut microbiome data sets. Comparison with the human microbiome revealed rumen-specific enrichment for genes encoding de novo synthesis of vitamin B12, ongoing evolution by gene loss and potential vertical inheritance of the rumen microbiome based on underrepresentation of markers of environmental stress. We estimate that our Hungate genome resource represents ∼75% of the genus-level bacterial and archaeal taxa present in the rumen.

3 May 2019 in Nature Communications
Verified
Journal Article
Open access
PDF file
PLPascal Lapébie
Pascal Lapébie
VLVincent Lombard
Vincent Lombard
EDElodie Drula
Elodie Drula
NTNicolas Terrapon
Nicolas Terrapon
BHBernard Henrissat
Bernard Henrissat
Unlike proteins, glycan chains are not directly encoded by DNA, but by the specificity of the enzymes that assemble them. Theoretical calculations have proposed an astronomical number of possible isomers (> 1012 hexasaccharides) but the actual diversity of glycan structures in nature is not known. Bacteria of the Bacteroidetes phylum are considered primary degraders of polysaccharides and they are found in all ecosystems investigated. In Bacteroidetes genomes, carbohydrate-degrading enzymes (CAZymes) are arranged in gene clusters termed polysaccharide utilization loci (PULs). The depolymerization of a given complex glycan by Bacteroidetes PULs requires bespoke enzymes; conversely, the enzyme composition in PULs can provide information on the structure of the targeted glycans. Here we group the 13,537 PULs encoded by 964 Bacteroidetes genomes according to their CAZyme composition. We find that collectively Bacteroidetes have elaborated a few thousand enzyme combinations for glycan breakdown, suggesting a global estimate of diversity of glycan structures much smaller than the theoretical one.

20 May 2014 in Nature Communications
Verified
Journal Article
Open access
PDF file
NTNicolas Terrapon
Nicolas Terrapon
CLCai Li
Cai Li
HRHugh M. Robertson
Hugh M. Robertson
LJLu Ji
Lu Ji
XMXuehong Meng
Xuehong Meng
JLJürgen Liebig
Jürgen Liebig
Although eusociality evolved independently within several orders of insects, research into the molecular underpinnings of the transition towards social complexity has been confined primarily to Hymenoptera (for example, ants and bees). Here we sequence the genome and stage-specific transcriptomes of the dampwood termite Zootermopsis nevadensis (Blattodea) and compare them with similar data for eusocial Hymenoptera, to better identify commonalities and differences in achieving this significant transition. We show an expansion of genes related to male fertility, with upregulated gene expression in male reproductive individuals reflecting the profound differences in mating biology relative to the Hymenoptera. For several chemoreceptor families, we show divergent numbers of genes, which may correspond to the more claustral lifestyle of these termites. We also show similarities in the number and expression of genes related to caste determination mechanisms. Finally, patterns of DNA methylation and alternative splicing support a hypothesized epigenetic regulation of caste differentiation.