Table 3.
Comparison of B. subtilis and E. coli as chassis for pyrazines biosynthesis.
| Attribute | B. subtilis | E. coli |
|---|---|---|
| Native pathway capacity | High (TTMP/alkylpyrazines via acetoin) | None (requires full heterologous pathway) |
| Max. reported titer | 13.37 g/L TTMP (Li et al., 2023) | 2.90 g/L 2,5-DMP (Liu et al., 2024) |
| Metabolic flexibility | Limited (alkylpyrazines dominant) | High (engineered for various pyrazines) |
| Key engineering targets | Precursor retention (bdhA, acoA) | Pathway assembly + Cofactor balancing (NADH/NADPH) |
| Process scalability | Robust in waste-based media (e.g., molasses) | Demands defined media; Sensitive to inhibitors |