"Candidatus Galacturonibacter soehngenii" Shows Acetogenic Catabolism of Galacturonic Acid but Lacks a Canonical Carbon Monoxide Dehydrogenase/Acetyl-CoA Synthase Complex

被引:5
作者
Valk, Laura C. [1 ]
Diender, Martijn [2 ]
Stouten, Gerben R. [1 ]
Petersen, Jette F. [3 ]
Nielsen, Per H. [3 ]
Dueholm, Morten S. [3 ]
Pronk, Jack T. [1 ]
van Loosdrecht, Mark C. M. [1 ]
机构
[1] Delft Univ Technol, Dept Biotechnol, Delft, Netherlands
[2] Wageningen Univ & Res, Lab Microbiol, Wageningen, Netherlands
[3] Aalborg Univ, Ctr Microbial Communities, Dept Chem & Biosci, Aalborg, Denmark
关键词
acetogenesis; C-13-labeling; meta-transcriptomics; chemostat enrichment culture; Wood-Ljungdahl pathway; HYBRID-CLUSTER PROTEIN; WOOD-LJUNGDAHL PATHWAY; IRON-SULFUR PROTEIN; RHODOSPIRILLUM-RUBRUM; DESULFOVIBRIO-VULGARIS; ESCHERICHIA-COLI; NICKEL; HYDROGENASE; METABOLISM; DATABASE;
D O I
10.3389/fmicb.2020.00063
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Acetogens have the ability to fixate carbon during fermentation by employing the Wood-Ljungdahl pathway (WLP), which is highly conserved across Bacteria and Archaea. In a previous study, product stoichometries in galacturonate-limited, anaerobic enrichment cultures of "Candidatus Galacturonibacter soehngenii," from a novel genus within the Lachnospiraceae, suggested the simultaneous operation of a modified Entner-Doudoroff pathway for galacturonate fermentation and a WLP for acetogenesis. However, a draft metagenome-assembled genome (MAG) based on short reads did not reveal homologs of genes encoding a canonical WLP carbon-monoxide-dehydrogenase/acetyl-Coenzyme A synthase (CODH/ACS) complex. In this study, (NaHCO3)-C-13 fed to chemostat-grown, galacturonate-limited enrichment cultures of "Ca. G. soehngenii" was shown to be incorporated into acetate. Preferential labeling of the carboxyl group of acetate was consistent with acetogenesis via a WLP in which the methyl group of acetate was predominately derived from formate. This interpretation was further supported by high transcript levels of a putative pyruvate-formate lyase gene and very low transcript levels of a candidate gene for formate dehydrogenase. Reassembly of the "Ca. G. soehngenii" MAG with support from long-read nanopore sequencing data produced a single-scaffold MAG, which confirmed the absence of canonical CODH/ACS-complex genes homologs. However, high CO-dehydrogenase activities were measured in cell extracts of "Ca. G. soehngenii" enrichment cultures, contradicting the absence of corresponding homologs in the MAG. Based on the highly conserved amino-acid motif associated with anaerobic Ni-CO dehydrogenase proteins, a novel candidate was identified which could be responsible for the observed activities. These results demonstrate operation of an acetogenic pathway, most probably as a yet unresolved variant of the Wood-Ljungdahl pathway, in anaerobic, galacturonate-limited cultures of "Ca. G. soehngenii."
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页数:12
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