A semisynthetic organism carries a third, engineered base pair — X:Y (modelled on Romesberg's dNaM:dTPT3) — spliced into an otherwise natural A·T / G·C genome. The cell cannot make the unnatural nucleoside triphosphates itself, so each division needs an external feed plus an algal nucleotide transporter (PtNTT2) to pull them across the membrane:
transport efficiency e = clamp(feed × transporter × 1.05, 0, 1)
loss rate per gen L = L_max × (1 − e) L_max = 35%
retention per gen p = 1 − L
population fraction F(g) = p^g (each cell decides independently, once lost it stays lost)
- Feed / transporter sliders — with both near 100% the effective loss rate collapses toward zero and the X:Y pair is copied faithfully generation after generation, exactly like the lab strain's improved retention.
- Advance Generation / Auto-play — each generation the visualised specimen cell and a 144-cell population sample independently roll against the retention probability; once a lineage loses X:Y it reverts permanently to a natural T·A pair — DNA repair has no template to restore the unnatural chemistry.
- Cut Feed — sets the external supply to zero, so loss rate jumps to L_max: this is the "genetic firewall" — an inherent biocontainment mechanism, since an escaped cell simply cannot propagate its expanded genetic code outside the lab.
Real-world relevance: this is the actual containment strategy behind Synthorx/Sanofi's semisynthetic biologics and the original Scripps Research organism — dependency on a synthetic nutrient, not a kill gene, keeps engineered genetic information from spreading into wild populations.