Bacterial genome replication at subzero temperatures in permafrost

Abstract Microbial metabolic activity occurs at subzero temperatures in permafrost, an environment representing ∼25% of the global soil organic matter. Although much of the observed subzero microbial activity may be due to basal metabolism or macromolecular repair, there is also ample evidence for c...

Full description

Bibliographic Details
Published in:The ISME Journal
Main Authors: Tuorto, Steven J, Darias, Phillip, McGuinness, Lora R, Panikov, Nicolai, Zhang, Tingjun, Häggblom, Max M, Kerkhof, Lee J
Format: Article in Journal/Newspaper
Language:English
Published: Oxford University Press (OUP) 2013
Subjects:
Online Access:http://dx.doi.org/10.1038/ismej.2013.140
http://www.nature.com/articles/ismej2013140.pdf
http://www.nature.com/articles/ismej2013140
https://academic.oup.com/ismej/article-pdf/8/1/139/56286340/41396_2014_article_bfismej2013140.pdf
Description
Summary:Abstract Microbial metabolic activity occurs at subzero temperatures in permafrost, an environment representing ∼25% of the global soil organic matter. Although much of the observed subzero microbial activity may be due to basal metabolism or macromolecular repair, there is also ample evidence for cellular growth. Unfortunately, most metabolic measurements or culture-based laboratory experiments cannot elucidate the specific microorganisms responsible for metabolic activities in native permafrost, nor, can bulk approaches determine whether different members of the microbial community modulate their responses as a function of changing subzero temperatures. Here, we report on the use of stable isotope probing with 13C-acetate to demonstrate bacterial genome replication in Alaskan permafrost at temperatures of 0 to −20 °C. We found that the majority (80%) of operational taxonomic units detected in permafrost microcosms were active and could synthesize 13C-labeled DNA when supplemented with 13C-acetate at temperatures of 0 to −20 °C during a 6-month incubation. The data indicated that some members of the bacterial community were active across all of the experimental temperatures, whereas many others only synthesized DNA within a narrow subzero temperature range. Phylogenetic analysis of 13C-labeled 16S rRNA genes revealed that the subzero active bacteria were members of the Acidobacteria, Actinobacteria, Chloroflexi, Gemmatimonadetes and Proteobacteria phyla and were distantly related to currently cultivated psychrophiles. These results imply that small subzero temperature changes may lead to changes in the active microbial community, which could have consequences for biogeochemical cycling in permanently frozen systems.