Decoding how a soil bacterium extracts building blocks and metabolic energy from ligninolysis provides road map for lignin valorization

Proc Natl Acad Sci U S A. 2016 Oct 4;113(40):E5802-E5811. doi: 10.1073/pnas.1606043113. Epub 2016 Sep 15.

Abstract

Sphingobium sp. SYK-6 is a soil bacterium boasting a well-studied ligninolytic pathway and the potential for development into a microbial chassis for lignin valorization. An improved understanding of its metabolism will help researchers in the engineering of SYK-6 for the production of value-added chemicals through lignin valorization. We used 13C-fingerprinting, 13C metabolic flux analysis (13C-MFA), and RNA-sequencing differential expression analysis to uncover the following metabolic traits: (i) SYK-6 prefers alkaline conditions, making it an efficient host for the consolidated bioprocessing of lignin, and it also lacks the ability to metabolize sugars or organic acids; (ii) the CO2 release (i.e., carbon loss) from the ligninolysis-based metabolism of SYK-6 is significantly greater than the CO2 release from the sugar-based metabolism of Escherichia coli; (iii) the vanillin catabolic pathway (which is the converging point of majority of the lignin catabolic pathways) is coupled with the tetrahydrofolate-dependent C1 pathway that is essential for the biosynthesis of serine, histidine, and methionine; (iv) catabolic end products of lignin (pyruvate and oxaloacetate) must enter the tricarboxylic acid (TCA) cycle first and then use phosphoenolpyruvate carboxykinase to initiate gluconeogenesis; and (v) 13C-MFA together with RNA-sequencing differential expression analysis establishes the vanillin catabolic pathway as the major contributor of NAD(P)H synthesis. Therefore, the vanillin catabolic pathway is essential for SYK-6 to obtain sufficient reducing equivalents for its healthy growth; cosubstrate experiments support this finding. This unique energy feature of SYK-6 is particularly interesting because most heterotrophs rely on the transhydrogenase, the TCA cycle, and the oxidative pentose phosphate pathway to obtain NADPH.

Keywords: 13C-MFA; NADPH; fingerprinting; gluconeogenesis; lignin.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acids / metabolism
  • Bacteria / genetics
  • Bacteria / growth & development
  • Bacteria / metabolism*
  • Benzaldehydes / chemistry
  • Benzaldehydes / metabolism
  • Carbon / metabolism
  • Carbon Isotopes
  • Energy Metabolism*
  • Gene Expression Profiling
  • Gene Expression Regulation, Bacterial
  • Hydrogen-Ion Concentration
  • Lignin / metabolism*
  • Metabolic Flux Analysis
  • NADP / metabolism
  • Sequence Analysis, RNA
  • Soil
  • Soil Microbiology*
  • Vanillic Acid / chemistry
  • Vanillic Acid / metabolism

Substances

  • Amino Acids
  • Benzaldehydes
  • Carbon Isotopes
  • Soil
  • NADP
  • Carbon
  • Lignin
  • vanillin
  • Vanillic Acid