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Table 2 Representative genome engineering strategies which could be applied to the enhancement of recombinant protein production in bacteria

From: Strain engineering for improved expression of recombinant proteins in bacteria

Method

Targeted cellular component

Target organism

Engineered phenotype

References

Global transcription machinery engineering (gTME)

General sigma factor σ70, stationary phase sigma factor σS, RNA polymerase a subunit

E. coli

Ethanol, butanol, isobutanol, pentanol, and 3-pentanol tolerance; lycopene, L-tyrosine, and hyaluronic acid production

[55, 66, 68]

 

Transcription factor Spt15p

S. cerevisiae

Ethanol tolerance and production

[67]

 

General sigma factor

Lactobacillus plantarum

lactic acid and hydrochloric acid tolerance

[95]

Libraries of artificial zinc fingers

Zinc fingers

S. cerevisiae

Tolerance to heat and osmotic stress; ketoconazole resistance

[69]

  

Mouse neuroblastoma cells

Neurogenesis, differentiation of neuroblasts to osteoblasts, proliferation rate

[69]

  

E. coli

Tolerance to heat, cold, and osmotic stress

[70, 71]

Trackable multiplex recombineering (TRMR)

> 95% of all individual E. coli genes

E. coli

Tolerance to salicin, D-fucose, methylglyoxal, valine, and lignocellulosic hydrolysate

[56]

Genome shuffling

Chromosome

Streptomyces fradiae

Tylosin production

[72]

  

A strain of Lactobacillus

Tolerance to lactic acid

[73]

  

Sphingobium chlorophenolicum

Degradation of pentachlorophenol

[74]