. 2005 Aug;71(8):4241–4247. doi: 10.1128/AEM.71.8.4241-4247.2005

TABLE 2.

Oligonucleotide primers

Primer	Sequence (5′-3′)
HtrAF	GGTCTAGACGCGCTGGTACAACTGG^a
HtrAR	TCGGATCCGTCGCCATTTGTATCAAC^a^,^c
HtrA-out	ACCGGAGAGCGCGCAACCAG^c
HtrASSF	AACGGATCCTGGTTATGTAAG^a
HtrASSR	ACGGTACCCGTTACCACTTC^a
HtrASSQ1F	CACCGTTTTTTTAAAGCTTTATTCATC GTTTTTTCATATTTGGGG^b
HtrASSQ1R	CCCCAAATATGAAAAAACGATGAATA AAGCTTTAAAAAAACGGT^b
DnaKF	GCTGGTCTTGAAGTAGAAC^c
DnaKR	GTTCATCAAATTTAGCACGAGT^c
GroELF	GTAGTAGCCGTGAAAGC^c
GroELR	GTAGAGCGGAACGTGTTAC^c
0291F	GATTGTGCTTTGAGTGGAAAG^c
0291R	CCCCCAACATCAATACCTTC^c
0293F	GTTGAAGTTCCGGATGAGAAA^c
0293R	CAACCTCATCAACTGGTGC^c

Restriction sites incorporated into primer sequences are underlined.

Frameshift mutation incorporated into primer sequence are underlined.

Primers used for transcriptional analysis.