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Table 1 List of nucleotide sequences used in this study

From: Downsizing a pullulanase to a small molecule with improved soluble expression and secretion efficiency in Escherichia coli

Primer name

Nucleotide sequence (5′ → 3′)

Enzyme

Gene

WT[F]

GGGAATTCCATATGGATTCTACTTCGACTAAAGTTATTGTTC

NdeI

BaPul

M1[F]

GGGAATTCCATATGCCATCTGTTTCAAATGCCTATCTTG

NdeI

BaPul-ΔCMB41

M2[F]

GGGAATTCCATATGGATTCTACTTCGACTAAAGTTATTGTTC

NdeI

BaPul-ΔX45

M3[F]

GGGAATTCCATATGGATTCTACTTCGACTAAAGTTATTGTTC

NdeI

BaPul-ΔX25

M4[F]

GGGAATTCCATATGGTAACTGCCGTTCTTGTTGGAGATTTAC

NdeI

BaPul-ΔCMB41ΔX45

M5[F]

GGGAATTCCATATGCCATCTGTTTCAAATGCCTATCTTG

NdeI

BaPul-ΔCMB41ΔX25

M6[F]

GGGAATTCCATATGGATTCTACTTCGACTAAAGTTATTGTTC

NdeI

BaPul-ΔX25ΔX45

pelB-M1[F]

CATGCCATGGATCCATCTGTTTCAAATGCCTATCTTG

NcoI

BaPul-ΔCMB41

pelB-M3[F]

CATGCCATGGATTCTACTTCGACTAAAGTTATTGTTC

NcoI

BaPul-ΔX25

pelB-M5[F]

CATGCCATGGATCCATCTGTTTCAAATGCCTATCTTG

NcoI

BaPul-ΔCMB41ΔX25

pelB-WT[F]

CATGCCATGGATTCTACTTCGACTAAAGTTATTGTTC

NcoI

BaPul

[R]a

CCGCTCGAGTTGTTTGAGAATAAGCGTACTTATAG

XhoI

 
  1. Italicized fonts indicate the recognition sites of the corresponding restriction enzymes
  2. [F] and [R] represent the forward and reverse primers, respectively
  3. a[R] was used as the reverse primer in all cases