Reyes-Caballero Hermes, Guerra Alfredo J, Jacobsen Faith E, Kazmierczak Krystyna M, Cowart Darin, Koppolu Uma Mahendra Kumar, Scott Robert A, Winkler Malcolm E, Giedroc David P
Department of Chemistry, Indiana University, Bloomington, IN 47405-7102, USA.
J Mol Biol. 2010 Oct 22;403(2):197-216. doi: 10.1016/j.jmb.2010.08.030. Epub 2010 Sep 8.
Streptococcus pneumoniae D39 AdcR (adhesin competence repressor) is the first metal-sensing member of the MarR (multiple antibiotic resistance repressor) family to be characterized. Expression profiling with a ΔadcR strain grown in liquid culture (brain-heart infusion) under microaerobic conditions revealed upregulation of 13 genes, including adcR and adcCBA, encoding a high-affinity ABC uptake system for zinc, and genes encoding cell-surface zinc-binding pneumococcal histidine triad (Pht) proteins and AdcAII (Lmb, laminin binding). The ΔadcR, H108Q and H112Q adcR mutant allelic strains grown in 0.2 mM Zn(II) exhibit a slow-growth phenotype and an approximately twofold increase in cell-associated Zn(II). Apo- and Zn(II)-bound AdcR are homodimers in solution and binding to a 28-mer DNA containing an adc operator is strongly stimulated by Zn(II) with K(DNA-Zn)=2.4 × 10(8) M(-1) (pH 6.0, 0.2 M NaCl, 25 °C). AdcR binds two Zn(II) per dimer, with stepwise Zn(II) affinities K(Zn1) and K(Zn2) of ≥10(9) M(-1) at pH 6.0 and ≥10(12) M(-1) at pH 8.0, and one to three lower affinity Zn(II) depending on the pH. X-ray absorption spectroscopy of the high-affinity site reveals a pentacoordinate N/O complex and no cysteine coordination, the latter finding corroborated by wild type-like functional properties of C30A AdcR. Alanine substitution of conserved residues His42 in the DNA-binding domain, and His108 and His112 in the C-terminal regulatory domain, abolish high-affinity Zn(II) binding and greatly reduce Zn(II)-activated binding to DNA. NMR studies reveal that these mutants adopt the same folded conformation as dimeric wild type apo-AdcR, but fail to conformationally switch upon Zn(II) binding. These studies implicate His42, His108 and H112 as metalloregulatory zinc ligands in S. pneumoniae AdcR.
肺炎链球菌D39 AdcR(黏附素能力阻遏蛋白)是MarR(多重抗生素抗性阻遏蛋白)家族中首个被鉴定的金属感应成员。在微需氧条件下,对在液体培养基(脑心浸液)中生长的ΔadcR菌株进行表达谱分析,结果显示13个基因上调,包括adcR和adcCBA,后者编码一种锌的高亲和力ABC摄取系统,以及编码细胞表面锌结合肺炎球菌组氨酸三联体(Pht)蛋白和AdcAII(Lmb,层粘连蛋白结合蛋白)的基因。在0.2 mM Zn(II)中生长的ΔadcR、H108Q和H112Q adcR突变等位基因菌株表现出生长缓慢的表型,且细胞相关的Zn(II)增加约两倍。溶液中的脱辅基和Zn(II)结合的AdcR均为同型二聚体,Zn(II)能强烈刺激其与含有adc操纵子的28聚体DNA结合,K(DNA-Zn)=2.4×10(8) M(-1)(pH 6.0,0.2 M NaCl,25 °C)。每个二聚体的AdcR结合两个Zn(II),在pH 6.0时,Zn(II)的逐步亲和力K(Zn1)和K(Zn2)≥10(9) M(-1),在pH 8.0时≥10(12) M(-1),且根据pH值还结合一到三个亲和力较低的Zn(II)。高亲和力位点的X射线吸收光谱显示为五配位的N/O络合物,不存在半胱氨酸配位,C30A AdcR的野生型样功能特性证实了后一发现。DNA结合结构域中保守残基His42以及C端调节结构域中His108和His112的丙氨酸取代消除了高亲和力的Zn(II)结合,并大大降低了Zn(II)激活的与DNA的结合。核磁共振研究表明,这些突变体与二聚体野生型脱辅基AdcR具有相同的折叠构象,但在结合Zn(II)时无法发生构象转换。这些研究表明His42、His108和H112是肺炎链球菌AdcR中的金属调节锌配体。