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Table 1 Strains and plasmids used in the study

From: Optimization of alkaline protease production by rational deletion of sporulation related genes in Bacillus licheniformis

Strain or plasmid

Characteristics or purpose

Reference

Strains

 E. coli EC135

Knockout vectors construction

Chinese Academy of Science

 E. coli EC135 pM.Bam

Plasmid DNA methylation modification

Chinese Academy of Science

 B. licheniformis 2709 Δupp (BL Δupp)

Parent host

This work

 B. licheniformis ΔsigF (BL ΔF)

ΔsigF, sigF gene deletion

This work

 B. licheniformis ΔsigE (BL ΔE)

ΔsigE, sig E gene deletion

This work

 B. licheniformis Δspo0A (BL Δ0A)

Δspo0A, spo0A gene deletion

This work

 B. licheniformis CsigF (BL CF)

sigF gene complementation

This work

 B. licheniformis CsigE (BL CE)

sigE gene complementation

This work

 B. licheniformis Cspo0A (BL C0A)

spo0A gene complementation

This work

Plasmids

 pWH1520

Shuttle expression vector, Ampr (E. coli) and Tetr (Bacillus): MCS

Nankai University

 pWHU

pWH1520, upr T gene, cas9 gene

This work

 pWHF

Knockout vector, spo IIAC gene deletion

This work

 pWHE

Knockout vector, sig E gene deletion

This work

 pWHA

Knockout vector, spo0A gene deletion

This work

 pWHCF

Backcrossed vector, spo IIAC gene complementation

This work

 pWHCE

Backcrossed vector, sig E gene complementation

This work

 pWHCA

Backcrossed vector, spo0A gene complementation

This work