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Table 1 Summary of genome editing efficiency of the transformants by using the CRISPR/Cas9, CRISPR/Cas12a-RVR, and CRISPR/Cas12a-RR systems

From: Development of the thermophilic fungus Myceliophthora thermophila into glucoamylase hyperproduction system via the metabolic engineering using improved AsCas12a variants

Host

straina

Target

genes

Elements in co-transformation

PAM sequences

No. of analysed

Transformants

Gene disruption efficiency (%)

MtWT

Mtstk-12

Cas9 + sgRNA + donor

TGG

20

75

Cas12a-RVR + crRNA + donor

TTTC

22

82

Cas12a-RR + crRNA + donor

TTCG

22

77

MtWT

Mtap3m

Cas9 + sgRNA + donor

AGG

18

61

Cas12a-RVR + crRNA + donor

TATA

20

70

Cas12a-RR + crRNA + donor

TTCC

19

68

MtWT

Mtdsc-1

Cas9 + sgRNA + donor

CGG

20

95

Cas12a-RVR + crRNA + donor

TATG

20

100

Cas12a-RR + crRNA + donor

TTCA

20

95

MtWT

Mtsah-2

Cas9 + sgRNA + donor

CGG

20

75

Cas12a-RVR + crRNA + donor

TATC

20

90

Cas12a-RR + crRNA + donor

TCCC

20

85

  1. aMtWT, M. thermophila wild type strain