TABLE 2.
Selected genes or operons regulated by CepR2
| Gene | Functiona | Transcriptional unitb | Change (fold) for K56-2cepR2b vs K56-2
|
|
|---|---|---|---|---|
| Microarrayc | qRT-PCR or RT-PCRd | |||
| BCAL1234 | Putative heat shock Hsp20-related protein | BCAL1234-BCAL1233 | −2.2 ± 0.5 | −17.9 ± 21 |
| BCAL1233 | Putative heat shock protein | −2.0 ± 0.5 | ||
| bclA | Lectin BclA | BCAM0186 | 2.9 ± 0.8 | 2.2 ± 0.1 |
| cepR2 | Orphan LuxR homolog CepR2 | 21.1 ± 3.4 | 170 ± 50 | |
| BCAM0189 | Putative AraC-family regulatory protein | 188 ± 46 | 26.7 ± 6.6 | |
| BCAM0190 | Putative aminotransferase, class III | 11.6 ± 0.9 | ||
| BCAM0191 | Putative nonribosomal peptide synthetase | BCAM0191-BCAM0190 | 9.5 ± 3.0 | —e |
| BCAM0192 | Conserved hypothetical protein | BCAM0192-BCAM0196 | 113 ± 27 | —e |
| BCAM0193 | Conserved hypothetical protein | 171 ± 74 | ||
| BCAM0194 | Hypothetical protein | 151 ± 48 | ||
| BCAM0195 | Putative nonribosomal peptide synthetase | 58.3 ± 62.1 | ||
| BCAM0196 | Conserved hypothetical protein | 80.5 ± 31.1 | ||
| BCAM0199 | Putative outer membrane efflux protein | BCAM0199-BCAM0202 | 2.5 ± 0.6 | —e |
| BCAM0200 | Putative secretion protein, HlyD family | 8.4 ± 5.6 | ||
| BCAM0201 | Putative transporter | 2.3 ± 0.8 | ||
| BCAM0202 | Hypothetical protein | 1.8 ± 0.2 | ||
| BCAM1290 | RpiR family transcriptional regulator | −1.7 ± 0.2 | −2.6 ± 2.0 | |
| BCAM1420 | Putative multidrug efflux protein | −2.3 ± 1.2 | −8.1 ± 0.3 | |
| BCAM2307 | Zinc metalloprotease ZmpB | −1.7 ± 0.7 | 2.6 ± 1.2f | |
| BCAS0293 | Nematocidal protein AidA | 1.7 ± 0.1 | 5.8 ± 2.9f | |
| BCAS0409 | Zinc metalloprotease ZmpA | 1.6 ± 0.3 | 1.2 ± 0.1f | |
Function derived from B. cenocepacia J2315 (33).
Transcriptional units were experimentally determined by RT-PCR.
Unless indicated otherwise, change (mean ± standard deviation) in 8-h cultures of K56-2cepR2b compared to 8-h cultures of K56-2 as determined by microarray analysis with at least two biological replicates.
Change (mean ± standard deviation) in 8-h cultures of K56-2cepR2b compared to 8-h cultures of K56-2 as determined by qRT-PCR.
Expression was measured by RT-PCR (see Fig. 3).
Expression was measured in cultures grown for 18 h.