Table 1.

Primers and conditions for PCR amplification of genetic element.

No.	Name	Sequence (5′–3′)	Tm (°C)	Target	Product size
1	rpoA1F	GCATTCCAGTCGATTCCATC	57	rpoA	560 bp
2	rpoA1R	CCAAGATCGCCTTCTGATGT
3	rpoA2F	GGACGTCGAAAGGAAGAAGA	57	rpoA	542 bp
4	rpoA2R	GTCTCCACGTCCAGGATCAG
5	rpoBF	GTAGTCCACGCCGTAAACGG	65	rpoB	601 bp
6	rpoBR	ACGTCCATGTAGTCCACCTCAG
7	rpoCF	CGAAAACCTCTACCGCGAAC	64	rpoC	650 bp
8	rpoCR	GCGACAGGATGTTGTTGGAG
9	inhAproF	ATCACCACCGCCGCTGAAGC	65	inhApro	650 bp
12	inhAproR	GTTCGGGTACCCGGGAATG
11	inhA1F	CTACATCGACACCGATATGAC	57	inhA	600 bp
12	inhA1R	GACCGTCATCCAGTTGTAG
13	inhA2F	GCATCAACCCGTTCTTCGAC	57	inhA	550 bp
14	inhA2R	TAATGCCATTGATCGGTGATAC
15	ahpCproF	ACCACTGCTTTGCCGCCACC	70	ahpCpro	340 bp
16	ahpCproR	CCGATGAGAGCGGTGAGCTG
17	katGF	CCAGCGGCCCAAGGTATC	65	katG	820 bp
18	katGR	GCTGTGGCCGGTCAAGAAGAAGT
19	ndhF	ATCACCACCGCCGCTGAAGC	64	ndh	589 bp
20	ndhR	GTTCGGGTACCCGGGAATG