Single-cell genomics reveals pyrrolysine-encoding potential in members of uncultivated archaeal candidate division MSBL1
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ArticleKAUST Department
Biological and Environmental Sciences and Engineering (BESE) DivisionBioscience Program
Computational Bioscience Research Center (CBRC)
Marine Science Program
Office of the VP
Red Sea Research Center (RSRC)
Date
2017-06-06Online Publication Date
2017-06-06Print Publication Date
2017-08Permanent link to this record
http://hdl.handle.net/10754/623647
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Show full item recordAbstract
Pyrrolysine (Pyl), the 22nd canonical amino acid, is only decoded and synthesized by a limited number of organisms in the domains Archaea and Bacteria. Pyl is encoded by the amber codon UAG, typically a stop codon. To date, all known Pyl-decoding archaea are able to carry out methylotrophic methanogenesis. The functionality of methylamine methyltransferases, an important component of corrinoid-dependent methyltransfer reactions, depends on the presence of Pyl. Here, we present a putative pyl gene cluster obtained from single-cell genomes of the archaeal Mediterranean Sea Brine Lakes group 1 (MSBL1) from the Red Sea. Functional annotation of the MSBL1 single cell amplified genomes (SAGs) also revealed a complete corrinoid-dependent methyl-transfer pathway suggesting that members of MSBL1 may possibly be capable of synthesizing Pyl and metabolizing methylated amines. This article is protected by copyright. All rights reserved.Citation
Guan Y, Haroon MF, Alam I, Ferry JG, Stingl U (2017) Single-cell genomics reveals pyrrolysine-encoding potential in members of uncultivated archaeal candidate division MSBL1. Environmental Microbiology Reports. Available: http://dx.doi.org/10.1111/1758-2229.12545.Sponsors
This study was supported by King Abdullah University of Science and Technology (KAUST) through baseline funding and the SEDCO Research Excellence award to US.Publisher
WileyPubMed ID
28493460Additional Links
http://onlinelibrary.wiley.com/doi/10.1111/1758-2229.12545/abstractae974a485f413a2113503eed53cd6c53
10.1111/1758-2229.12545
Scopus Count
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