Loo C Y, Mitrakul K, Voss I B, Hughes C V, Ganeshkumar N
Department of Pediatric Dentistry, Goldman School of Dental Medicine, Boston University, Boston, Massachusetts 02118, USA.
J Bacteriol. 2003 May;185(9):2887-900. doi: 10.1128/JB.185.9.2887-2900.2003.
Pioneer oral bacteria, including Streptococcus gordonii, initiate the formation of oral biofilms on tooth surfaces, which requires differential expression of genes that recognize unique environmental cues. An S. gordonii::Tn917-lac biofilm-defective mutant was isolated by using an in vitro biofilm formation assay. Subsequent inverse PCR and sequence analyses identified the transposon insertion to be near the 3' end of an open reading frame (ORF) encoding a protein homologous to a Streptococcus pneumoniae repressor, AdcR. The S. gordonii adc operon, consisting of the four ORFs adcR, adcC, adcB, and adcA, is homologous to the adc operon of S. pneumoniae, which plays a role in zinc and/or manganese transport and genetic competence in S. pneumoniae. AdcR is a metal-dependent repressor protein containing a putative metal-binding site, AdcC contains a consensus-binding site for ATP, AdcB is a hydrophobic protein with seven hydrophobic membrane-spanning regions, and AdcA is a lipoprotein permease with a putative metal-binding site. The three proteins (AdcC through -A) are similar to those of the binding-lipoprotein-dependent transport system of gram-positive bacteria. Reverse transcriptase PCR confirmed that adcRCBA are cotranscribed as an operon in S. gordonii and that the transposon insertion in S. gordonii adcR::Tn917-lac had resulted in a polar mutation. Expression of adcR, measured by the beta-galactosidase activity of the adcR::Tn917-lac mutant, was growth phase dependent and increased when the mutant was grown in media with high levels of manganese (>1 mM) and to a lesser extent in media with zinc, indicating that AdcR may be a regulator at high levels of extracellular manganese. A nonpolar inactivation of adcR generated by allelic replacement resulted in a biofilm- and competence-defective phenotype. The biofilm-defective phenotype observed suggests that AdcR is an active repressor when synthesized and acts at a distant site(s) on the chromosome. Thus, the adc operon is involved in manganese acquisition in S. gordonii and manganese homeostasis and appears to modulate sessile growth in this bacterium.
包括戈登氏链球菌在内的先驱口腔细菌会在牙齿表面引发口腔生物膜的形成,这需要识别独特环境线索的基因进行差异表达。通过体外生物膜形成试验分离出一株戈登氏链球菌::Tn917 - lac生物膜缺陷型突变体。随后的反向PCR和序列分析确定转座子插入位于一个开放阅读框(ORF)的3'端附近,该开放阅读框编码一种与肺炎链球菌阻遏蛋白AdcR同源的蛋白质。戈登氏链球菌的adc操纵子由四个开放阅读框adcR、adcC、adcB和adcA组成,与肺炎链球菌的adc操纵子同源,后者在肺炎链球菌的锌和/或锰转运以及遗传感受态中发挥作用。AdcR是一种金属依赖性阻遏蛋白,含有一个假定的金属结合位点,AdcC含有一个ATP的共有结合位点,AdcB是一种具有七个疏水跨膜区域的疏水蛋白,AdcA是一种具有假定金属结合位点的脂蛋白通透酶。这三种蛋白质(AdcC至 -A)与革兰氏阳性细菌的结合脂蛋白依赖性转运系统中的蛋白质相似。逆转录酶PCR证实adcRCBA在戈登氏链球菌中作为一个操纵子共转录,并且戈登氏链球菌adcR::Tn917 - lac中的转座子插入导致了极性突变。通过adcR::Tn917 - lac突变体的β - 半乳糖苷酶活性测量的adcR表达与生长阶段相关,当突变体在含有高水平锰(>1 mM)的培养基中生长时表达增加,在含有锌的培养基中增加程度较小,这表明AdcR可能是细胞外锰水平较高时的一种调节因子。通过等位基因替换产生的adcR非极性失活导致了生物膜和感受态缺陷型表型。观察到的生物膜缺陷型表型表明,AdcR在合成时是一种活性阻遏蛋白,并在染色体上的远处位点起作用。因此,adc操纵子参与了戈登氏链球菌中的锰获取和锰稳态,并且似乎调节了这种细菌的固着生长。