Weng Shu-Fen, Lin Juey-Wen, Chen Chih-Hung, Chen Yih-Yuan, Tseng Yi-Hsuan, Tseng Yi-Hsiung
Institute of Molecular Biology, National Chung Hsing University, Taichung 402, Taiwan, Republic of China.
Antimicrob Agents Chemother. 2004 Jan;48(1):209-15. doi: 10.1128/AAC.48.1.209-215.2004.
Sequencing of the upstream region of the beta-lactamase gene from Xanthomonas campestris pv. campestris 11 (bla(XCC-1)) revealed the cognate ampR1 gene (289 amino acids, 31 kDa). It runs divergently from bla(XCC-1) with a 100-bp intergenic region (IG) containing partially overlapped promoters with structural features typical of the bla-ampR IG. The deduced AmpR1 protein shows significant identity in amino acid sequence and conserved motifs with AmpR proteins of other species, e.g., of Pseudomonas aeruginosa (58.2% amino acid identity). Results of insertional mutation, complementation tests, and beta-lactamase assays suggested that expression of bla(XCC-1) was constitutive and dependent on AmpR1. Four bla genes and two ampR genes are present in the fully sequenced X. campestris pv. campestris ATCC 33913 genome, with XCC3039 and XCC3040 considered the analogues of bla(XCC-1) and ampR1, respectively. An ampR1 homologue was detected by Southern hybridization in the ampicillin-resistant Xanthomonas strains, which appear to express beta-lactamase constitutively. Although the significance remains to be studied, constitutive expression of beta-lactamase by a widespread bacterial genus raises environmental concerns regarding the dissemination of resistance genes.
对野油菜黄单胞菌野油菜致病变种11(bla(XCC - 1))的β-内酰胺酶基因上游区域进行测序,发现了同源的ampR1基因(289个氨基酸,31 kDa)。它与bla(XCC - 1)反向转录,间隔区(IG)为100 bp,包含部分重叠的启动子,具有bla - ampR间隔区典型的结构特征。推导的AmpR1蛋白在氨基酸序列和保守基序方面与其他物种的AmpR蛋白具有显著同源性,例如铜绿假单胞菌(氨基酸同源性为58.2%)。插入突变、互补试验和β-内酰胺酶检测结果表明,bla(XCC - 1)的表达是组成型的且依赖于AmpR1。在全序列测定的野油菜黄单胞菌野油菜致病变种ATCC 33913基因组中存在4个bla基因和2个ampR基因,其中XCC3039和XCC3040分别被认为是bla(XCC - 1)和ampR1的类似物。通过Southern杂交在耐氨苄青霉素的黄单胞菌菌株中检测到一个ampR1同源物,这些菌株似乎组成型表达β-内酰胺酶。尽管其意义仍有待研究,但一个广泛存在的细菌属组成型表达β-内酰胺酶引发了对耐药基因传播的环境担忧。