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. 2017 Dec 1;7:16800. doi: 10.1038/s41598-017-17118-2

Table 2.

Primers used in the present study.

Primer Sequence 5′-3′ Amplified DNA
Phusion PCR for carB disruption
carBcrispfuz1 CTGTGCAGGTGCCAGCGCATCACC carB promoter and coding sequence upstream from protospacer
carBcrispfuz2 GGTGGTCTTGAATGCGCTCGTCCAG
carBcrispfuz3 TGGAGCTGCTGCGATGCGACAAC carB coding sequence downstream from protospacer
carBcrispfuz4 GTCTTGCTCTTCATATGACCAATAG
carBcrispfuz5 CCGATCTGGACGAGCGCATTCAAGACCACCTGCCTCAGCATTGGTACTTG pyrG with own promoter and terminator sequences
carBcrispfuz6 GTAGTTGTTGTCGCATCGCAGCAGCTCCAGTACACTGGCCATGCTATCG
carBcrispfuz7 CTTGTGGTAGACAATGTAGTTGTC phusion pcr product
carBcrispfuz8 CGTCAAAGCTCTCCTGATAAGCCTC
Primers for analysis of the carB mutants
MccarRPfw ATGCTGCTCACCTACATGGAAG carRP
MccarRPrev2 TTAAATGGTATTTAGATTTCTCA
MccarB1 ATGTCCAAGAAACACATTGTCATTA carB
MccarB2 TTAAATGACATTAGAGTTATGAACG
MccarBupfw TAGCCAATGACAGCGGTGACGC upstream region from protospacer
MccarBuprev GTTGTCGCATCGCAGCAGCTCCA
MccarBdwfw TGGAGCTGCTGCGATGCGACAAC downstream region from protospacer
MccarBdwrev CGTCAAAGCTCTCCTGATAAGCCTC
Phusion PCR for hmgR 2 disruption
h2p1 ACGGAGCAAGTTTACATTCATACC hmgR2 promoter and coding region upstream from protospacer
h2p2 GATTGGCGGTCTATCATATTTCAG
h2p3 CTCAACATCTCTTGTACTATGCCC hmgR2 coding sequence downstream from protospacer
h2p4 ATACGTTTGTACCGATGAAGGGA
h2pyrG5 CTCATTGCTGAAATATGATAGACCGCCAATCGTACAATTCCCTGCCTTCTGGAAG pyrG with own promoter and terminator seqences
h2pyrG6 CGATACAGGGCATAGTACAAGAGATGTTGAGCGCGTGAAAGACCTGCCTTGACTC
h2p7 TGTGAAATTGGCCTATAATCAGCCT phusion pcr product
h2p8 GGACAGACATTCCATCGTATACAG
Primers for analysis of the hmgR 2 mutant
h2cdns1 ATGTTGAAAAACGTCAAAAAAGAT hmgR2
h2cdns2 CTATGATTTAATACAACTTCCA
Primers used in the qPCR experiment
MCactinF CACTCCTTCACTACCACCGCTGA 117 bp of actin
MCactinR GAGAGCAGAGGATTGAGCAGCAG
H2_RT_F CTCGTATCATCTGTGCCTCTG 107 bp of hmgR2
H2_RT_R AGCAGTGTTACGGTTGTGAG