Newly discovered Asgard archaea Hermodarchaeota potentially degrade alkanes and aromatics via alkyl/benzyl-succinate synthase and benzoyl-CoA pathway.
Jia-Wei ZhangHong-Po DongLi-Jun HouYang LiuYa-Fei OuYan-Ling ZhengPing HanXia LiangGuo-Yu YinDian-Ming WuMin LiuYuhan HuangPublished in: The ISME journal (2021)
Asgard archaea are widely distributed in anaerobic environments. Previous studies revealed the potential capability of Asgard archaea to utilize various organic substrates including proteins, carbohydrates, fatty acids, amino acids and hydrocarbons, suggesting that Asgard archaea play an important role in sediment carbon cycling. Here, we describe a previously unrecognized archaeal phylum, Hermodarchaeota, affiliated with the Asgard superphylum. The genomes of these archaea were recovered from metagenomes generated from mangrove sediments, and were found to encode alkyl/benzyl-succinate synthases and their activating enzymes that are similar to those identified in alkane-degrading sulfate-reducing bacteria. Hermodarchaeota also encode enzymes potentially involved in alkyl-coenzyme A and benzoyl-coenzyme A oxidation, the Wood-Ljungdahl pathway and nitrate reduction. These results indicate that members of this phylum have the potential to strictly anaerobically degrade alkanes and aromatic compounds, coupling the reduction of nitrate. By screening Sequence Read Archive, additional genes encoding 16S rRNA and alkyl/benzyl-succinate synthases analogous to those in Hermodarchaeota were identified in metagenomic datasets from a wide range of marine and freshwater sediments. These findings suggest that Asgard archaea capable of degrading alkanes and aromatics via formation of alkyl/benzyl-substituted succinates are ubiquitous in sediments.
Keyphrases
- ionic liquid
- heavy metals
- amino acid
- polycyclic aromatic hydrocarbons
- fatty acid
- visible light
- nitric oxide
- organic matter
- room temperature
- signaling pathway
- wastewater treatment
- drinking water
- microbial community
- molecular docking
- single cell
- high intensity
- hydrogen peroxide
- transcription factor
- rna seq
- genome wide identification