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Table 3 The optimal solution for multi-synthesis maximization by E. coli

From: Multi-objective optimization of enzyme manipulations in metabolic networks considering resilience effects

ε-value

v P E P C * v P E P C b a s a l

v S E R S * v S E R S b a s a l

v D A H P S * v D A H P S b a s a l

Modulated enzymes

Optimal objective value ( η D * )

1

1.271

1.081

1.560

PK

0.970

 

1.342

1.068

1.780

G6PDH

0.975

2

1.248

1.518

1.652

G6PDH, SERS

0.846

 

1.211

1.409

1.456

PK, SERS

0.878†

 

1.778

1.106

2.185

PK, G6PDH

0.969

3

1.578

1.860

2.027

G6PDH, PK, SERS

0.782

 

1.388

1.730

1.872

G6PDH, SERS, RPPK

0.814†

4

1.801

1.973

2.225

G6PDH, PK, SERS, RPPK

0.778

 

1.492

1.934

2.175

G6PDH, PK, SERS, DAHPS

0.787†

5

1.597

2.258

2.467

G6PDH, PK, SERS, RPPK, DAHPS

0.763

 

1.958

2.134

2.322

G6PDH, PK, SERS, RPPK, SYN1

0.786

  1. The optimal enzymatic modulation to maximize aromatic amino acid, serine, and oxaloacetate synthesis rates simultaneously by E. coli without considering cell viability constraints. γ x i L B and γ e i L B are set to 0.2. γ x i U B and γ e i U B are set to 5.0. The superscript * means optimal solution, † denotes that the solution is not a Pareto solution, and ε is the number of allowed manipulated genes.