Models / KEA3 - tomato

Tomato KEA3 model

The tomato KEA3 model is a non-photochemical quenching (NPQ) model adapted for tomato (Solanum lycopersicum) from the original Arabidopsis NPQ model. It tracks the photosystem II reaction-centre states, plastoquinone redox, lumenal proton and potassium balance, ATP synthesis, PsbS protonation and the xanthophyll cycle.

The KEA3 K⁺/H⁺ antiporter shapes the proton motive force and thus the kinetics of photoprotection, and the model supports PAM fluorescence protocols to reproduce the resulting quenching dynamics.

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PAM Fluorescence - NPQ results

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1000
lumen_volume_per_area_membrane
molChl_per_area_membrane

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2.302585092994046
F
T

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1000
K_lumen_conc_initial
molChl_per_area_membrane

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1000
K_stroma_conc_initial
molChl_per_area_membrane

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Generated LaTeX Code

\begin{align*}
  \frac{d B0}{dt} &= - 2 \cdot B0 \cdot PPFD \\
  & + 2 \cdot B1 \cdot (kH0 + Quencher act. \cdot kH\_Qslope) \\
  & + 2 \cdot B1 \cdot kF \\
  & + 2 \cdot B2 \cdot PQ \cdot kPQH2 - \frac{B0 \cdot PQH2 \cdot kPQH2}{Keq\_PQH2} \\ 
  \frac{d B1}{dt} &= 2 \cdot B0 \cdot PPFD \\
  & - 2 \cdot B1 \cdot (kH0 + Quencher act. \cdot kH\_Qslope) \\
  & - 2 \cdot B1 \cdot kF - 2 \cdot 0.5 \cdot B1 \cdot kP \\ 
  \frac{d B2}{dt} &= 2 \cdot 0.5 \cdot B1 \cdot kP \\
  & - 2 \cdot B2 \cdot PQ \cdot kPQH2 - \frac{B0 \cdot PQH2 \cdot kPQH2}{Keq\_PQH2} \\
  & - 2 \cdot B2 \cdot PPFD + 2 \cdot B3 \cdot kF \\
  & + 2 \cdot B3 \cdot (kH0 + Quencher act. \cdot kH\_Qslope) \\ 
  \frac{d PQH2}{dt} &= B2 \cdot PQ \cdot kPQH2 - \frac{B0 \cdot PQH2 \cdot kPQH2}{Keq\_PQH2} \\
  & - PQH2 \cdot (O2ex \cdot kPTOX + \frac{Keqcytb6f \cdot PPFD \cdot k\_cytb6f}{1 + Keqcytb6f}) - \frac{PPFD \cdot k\_cytb6f \cdot (PQtot - PQH2)}{1 + Keqcytb6f} \\ 
  \frac{d ATP}{dt} &= ATP\_pmf\_act \cdot ATPactivity \cdot kATPsynthase \cdot (ADP - \frac{ATP}{KeqATPsyn}) \\
  & - ATP \cdot kATPconsumption \\ 
  \frac{d H\_lumen}{dt} &= \frac{2}{bH} \cdot 0.5 \cdot B1 \cdot kP \\
  & + \frac{4}{bH} \cdot PQH2 \cdot (O2ex \cdot kPTOX + \frac{Keqcytb6f \cdot PPFD \cdot k\_cytb6f}{1 + Keqcytb6f}) - \frac{PPFD \cdot k\_cytb6f \cdot (PQtot - PQH2)}{1 + Keqcytb6f} \\
  & - \frac{HPR}{bH} \cdot ATP\_pmf\_act \cdot ATPactivity \cdot kATPsynthase \cdot (ADP - \frac{ATP}{KeqATPsyn}) \\
  & - \frac{1}{bH} \cdot kleak \cdot (H\_lumen\_conc - H\_stroma\_conc) \\
  & - \frac{1}{bH} \cdot \max(0, \frac{1000 \cdot k\_KEA3 \cdot reg\_KEA3 \cdot stroma\_volume\_per\_area\_membrane \cdot (H\_lumen\_conc \cdot K\_stroma\_conc - H\_stroma\_conc \cdot K\_lumen\_conc)}{molChl\_per\_area\_membrane}) \\
  & + \frac{1}{bH} \cdot \max(0, \frac{1000 \cdot k\_KEA3 \cdot lumen\_volume\_per\_area\_membrane \cdot reg\_KEA3 \cdot (H\_stroma\_conc \cdot K\_lumen\_conc - H\_lumen\_conc \cdot K\_stroma\_conc)}{molChl\_per\_area\_membrane}) \\ 
  \frac{d delta\_psi}{dt} &= \frac{2 \cdot volts\_per\_charge}{bH} \cdot 0.5 \cdot B1 \cdot kP \\
  & + \frac{4 \cdot volts\_per\_charge}{bH} \cdot PQH2 \cdot (O2ex \cdot kPTOX + \frac{Keqcytb6f \cdot PPFD \cdot k\_cytb6f}{1 + Keqcytb6f}) - \frac{PPFD \cdot k\_cytb6f \cdot (PQtot - PQH2)}{1 + Keqcytb6f} \\
  & - \frac{HPR \cdot volts\_per\_charge}{bH} \cdot ATP\_pmf\_act \cdot ATPactivity \cdot kATPsynthase \cdot (ADP - \frac{ATP}{KeqATPsyn}) \\
  & - \frac{volts\_per\_charge}{bH} \cdot kleak \cdot (H\_lumen\_conc - H\_stroma\_conc) \\ 
  \frac{d Vx}{dt} &= - \frac{Vx \cdot kDeepoxV \cdot {H\_lumen}^{nHX}}{{H\_lumen}^{nHX} + {\frac{1000 \cdot lumen\_volume\_per\_area\_membrane \cdot {10}^{- KphSatZ}}{molChl\_per\_area\_membrane}}^{nHX}} \\
  & + Zx \cdot kEpoxZ \\ 
  \frac{d PsbS}{dt} &= - \frac{PsbS \cdot kProt \cdot {H\_lumen}^{nHL}}{{H\_lumen}^{nHL} + {\frac{1000 \cdot lumen\_volume\_per\_area\_membrane \cdot {10}^{- KphSatLHC}}{molChl\_per\_area\_membrane}}^{nHL}} \\
  & + PsbSP \cdot PsbS\_deprot\_act \cdot kDeprot \\ 
  \frac{d ATPactivity}{dt} &= \begin{cases}kActATPase \cdot (1 - ATPactivity) & PPFD > 0 \\ - ATPactivity \cdot kDeactATPase & \text{else}\end{cases} \\ 
  \frac{d K\_lumen}{dt} &= \max(0, \frac{1000 \cdot k\_KEA3 \cdot reg\_KEA3 \cdot stroma\_volume\_per\_area\_membrane \cdot (H\_lumen\_conc \cdot K\_stroma\_conc - H\_stroma\_conc \cdot K\_lumen\_conc)}{molChl\_per\_area\_membrane}) \\
  & - \max(0, \frac{1000 \cdot k\_KEA3 \cdot lumen\_volume\_per\_area\_membrane \cdot reg\_KEA3 \cdot (H\_stroma\_conc \cdot K\_lumen\_conc - H\_lumen\_conc \cdot K\_stroma\_conc)}{molChl\_per\_area\_membrane}) \\ 
  \frac{d K\_stroma}{dt} &= - \max(0, \frac{1000 \cdot k\_KEA3 \cdot reg\_KEA3 \cdot stroma\_volume\_per\_area\_membrane \cdot (H\_lumen\_conc \cdot K\_stroma\_conc - H\_stroma\_conc \cdot K\_lumen\_conc)}{molChl\_per\_area\_membrane}) \\
  & + \max(0, \frac{1000 \cdot k\_KEA3 \cdot lumen\_volume\_per\_area\_membrane \cdot reg\_KEA3 \cdot (H\_stroma\_conc \cdot K\_lumen\_conc - H\_lumen\_conc \cdot K\_stroma\_conc)}{molChl\_per\_area\_membrane})
\end{align*}

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