Cytochromes as microbial electron ‘wires’ — and how on-site qPCR turns this into decisions
Cytochromes are heme proteins that carry electrons. In many bacteria, multi-heme c-type cytochromes form chains that conduct electrons across the cell envelope to solids (minerals, metals, electrodes). We outline the science, why it matters for MIC, and how MICBUSTERS’ on-site qPCR makes it actionable.
What is a cytochrome?
A cytochrome is a hemoprotein whose heme cycles between Fe(II)/Fe(III), enabling electron transfer. Classes (a, b, c) refer to heme type/binding; c-types are covalently bound via the CXXCH motif. In bacteria, membrane- and surface-exposed cytochromes underpin respiration and extracellular electron transfer (EET).
From single heme to ‘heme wires’: multi-heme c-types
Multi-heme cytochromes stack several hemes within one polypeptide. Efficient electron flow emerges from heme–heme coupling and a graded set of redox potentials. Canonical systems include:
- Shewanella (Mtr/Omc): MtrA (periplasm), MtrC/OmcA (outer membrane, decaheme), plus a β-barrel conduit to the surface.
- Geobacter (OmcS/OmcZ): outer-surface cytochromes forming nanowires; OmcZ filaments exhibit high conductivity and support large current densities.
- Desulfovibrio (SRB): periplasmic cytochrome c3 (tetraheme) interfaces with hydrogenases and Hmc complexes toward sulfate reduction.
Cytochromes in EET: direct, mediated, hybrid
Multi-heme cytochromes enable direct transfer to/from solids; mediated routes via soluble shuttles (e.g., flavins) extend reach. Real biofilms often run a hybrid of both.
Why this matters for MIC
In MIC, the cathodic step frequently limits overall rates. Surface cytochromes can draw electrons from metals/conductive films more efficiently, raising cathodic current and corrosion.
- Current → loss (rule-of-thumb): 1 µA/cm² ≈ 0.011–0.012 mm/y uniform loss; +10 µA/cm² ≈ +0.12 mm/y (order-of-magnitude; pitting can exceed this).
- Consortia: EET-active, cytochrome-rich bacteria can coexist with methanogen-linked routes (e.g., micH), jointly aggravating corrosion.
- Films/minerals: FeS, magnetite and other conductive phases can bridge cytochromes to metal, shaping MIC kinetics.
MICBUSTERS on-site qPCR: making cytochrome-EET actionable
The practical question is: “Do we host a cytochrome-rich, EET-active community that elevates MIC risk?” Our on-site qPCR answers this within hours, via:
1) Marker panel (asset-specific)
- EET/cytochrome genes: outer-membrane/periplasmic markers such as mtrC/omcA (Shewanella), omcS/omcZ (Geobacter), hmc complex (Desulfovibrio).
- Community anchors: bacterial/archaeal 16S rRNA plus functional targets (e.g., mcrA for methanogens); optional micH for methanogen-linked corrosion.
- Assay design: degenerate primers as needed, matrix-validated efficiency/specificity (melt curves or probe assays).
2) Quantification & normalization
- Absolute qPCR: standard curves; report as gene copies per mL (fluids/sludge) or per cm² (biofilm/coupons).
- Relative indices: normalize EET markers to 16S to compute an Cytochrome-EET Index (CEI) (sum or weighted sum of mtrC/omcA/omcS/omcZ/hmc vs 16S).
- Live fraction (optional): PMA-qPCR to distinguish intact cells from relic DNA.
3) Reporting to decisions
- Trends & heatmaps: CEI, 16S load, functional markers across time and location.
- Electrochemistry linkage: Rising CEI concurrent with increased cathodic current supports an EET-driven MIC hypothesis.
- Action bands (heuristics; calibrate on site):
- Low/stable CEI + low Icath → routine monitoring.
- Rising/high CEI + moderate Icath → targeted tests (biofilm/cathode assays).
- High CEI + high Icath (>~13 µA/cm² ≈ >0.15 mm/y) → escalate mitigation; verify impact with qPCR + ER/coupons.
From genes to mm/y
qPCR quantifies capacity, not current. By co-trending CEI with cathodic current/potential and metal-loss (ER/coupons), site-specific models convert biology into predicted mm/y and document mitigation impact within a single maintenance window.
References (selected)
- Shi L. et al. (2016) Extracellular electron transfer mechanisms between microorganisms and minerals. Nat Rev Microbiol.
- Breuer M., Rosso K.M., Blumberger J. (2014) Electron flow in multiheme bacterial cytochromes. PNAS.
- Gu Y. et al. (2023) Structure & conductivity of Geobacter OmcZ nanowires. Nat Microbiol.
- Marsili E. et al. (2008) Flavin-mediated EET in Shewanella. PNAS.
- Valente F.M.A. et al. (2001) Tetraheme cytochrome c3 in Desulfovibrio. J Bacteriol.
- Lahme S. et al. (2021) Severe corrosion linked to methanogens via micH. Appl Environ Microbiol.
- Knisz J. et al. (2023) MIC—more than microbes. FEMS Microbiol Rev.
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