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Table 2 List of primers (with sequences) used in cloning, confirmation of mltG gene deletion and qRT-PCR analyses

From: mltG gene deletion mitigated virulence potential of Streptococcus mutans: An in-vitro, ex-situ and in-vivo study

Function

Primer name

Forward sequence (5′ → 3′)

Reverse sequence (3′ → 5′)

Cloning

mltG-up

TACTCGAGATGCTGTCTATGTCTTTATG

ATCTGCAGCATAACAGTTCGTGTTTCTT

mltG-dw

ATGGATCCGATGATCTTTATTTTGTAGCC

ATGTCGACTATTTTCTACGTCTACGCTA

Kan

ATAGGAGGGATTTATATGAGCCATATTCAA

TTAGAAGAACTCATCCATGGATGTCTGGAG

Transformation

analysis

mltG

ATACTCGAGATGAAAAAGGCTAAGCAATC

ATTGGATCCTTACGAATCACTGCTTGA

qRT-PCR

fruA

AGCAGATCAAACTACAGAGCCTACTG

GGACTGCTCGCACCATCA

gtfC

GGTTTAACGTCAAAATTAGCTGTATTAGC

CTCAACCAACCGCCACTGTT

clpA

TTTTGGGAGGCCTGTTGCT

TGGCAACGGAGGCAATAATC

spaP

GACTTTGGTAATGGTTATGCATCAA

TTTGTATCAGCCGGATCAAGTG

vic

TGACACGATTACAGCCTTTGATG

CGTCTAGTTCTGGTAACATTAAGTCCAAT

atpA

TCTGCCCGAGAAAGATCGA

GACCATTGTTGCGGATTCG

atpC

TGGAATGGGATCGGACTTTTT

TCCAACCCACGTAATTCAAAGG

ropA

GCGGTCGCTAATGCTGAAAT

CACGTTGGACCTCATCATGAA

comCD

ACAATTCCTTGAGTTCCATCCAAG

TGGTCTGCTGCCTGTTGC

ccpA

GCCAACTCATCCTCAGCAACA

GCGCAGCGTGTCATTAATTC

ftsX

GCAGCAAGATTTGGATTG

GCTTGGGTTGGTCTTATT

murE

TGCCGACCAGCCACATGATTTC

AGGCAGCAGCAACTGCATTTTC

murN

GAGGCTGGCAATCATAAA

CGCAGAGAATACAGTGATAA

gbpB

ATGGCGGTTATGGACACGTT

TTTGGCCACCTTGAACACCT