Nabedryk E, Breton J, Hienerwadel R, Fogel C, Mäntele W, Paddock M L, Okamura M Y
Département de Biologie Cellulaire et Moléculaire, CEA-Saclay, Gif-sur-Yvette, France.
Biochemistry. 1995 Nov 14;34(45):14722-32. doi: 10.1021/bi00045a013.
In order to investigate the changes of protonation or environment of carboxylic residues occurring upon photoreduction of the secondary quinone acceptor (QB) in the reaction center (RC) of the photosynthetic bacteria Rhodobacter sphaeroides 2.4.1., we have performed light-induced Fourier transform infrared (FTIR) spectroscopy on RCs from wild-type (Wt) and several site-directed mutants. The FTIR QB-/QB spectra have been obtained at pH 7 upon single-saturating flash excitation for native RCs and RC mutants containing either a single-site mutation, with Gln at L212 (EQ L212), Asn at L213 (DN L213), or Asn at L210 (DN L210), or a double-site mutation with both Gln at L212 and Asn at L213 (EQ L212 + DN L213). The assignment of an IR band to the protonation/deprotonation of a particular carboxylic side chain was analyzed by combining the effects of site-directed mutagenesis and 1H/2H isotope exchange. A positive band at 1728 cm-1 in the QB-/QB spectra was observed in Wt, DN L213, and DN L210 and was absent in the mutants EQ L212 and EQ L212 + DN L213. The intensity of the 1728 cm-1 band was significantly reduced in 2H2O, and a new feature appears at 1717 +/- 1 cm-1. Furthermore, the amplitude of the 1728 cm-1 band was similar in native and DN L210 RCs but was increased in DN L213. This band is attributed to partial proton uptake by Glu L212 estimated to be 0.3-0.4 H+/QB- in native and DN L210 RCs and O.5-0.6 H+/QB- in DN L213 RCs. In contrast, the FTIR QB-/QB spectra show no evidence for change of protonation or environment of Asp L213 upon QB- formation. The increased protonation of Glu L212 in DN L213 RCs is explained by a decreased Glu L212 pKa value due to the loss of a negatively charged Asp L213. Part of a small differential signal at 1732 (+)/1740 (-) cm-1 that is affected by 1H/2H exchange is tentatively assigned to an environmental shift of the protonated Asp L210. A negative signal at 1685 cm-1 is propose to arise from the absorption change of the amide I carbonyl mode of Glu L212.(ABSTRACT TRUNCATED AT 400 WORDS)
为了研究光合细菌球形红杆菌2.4.1反应中心(RC)中次级醌受体(QB)光还原时羧基残基的质子化或环境变化,我们对野生型(Wt)和几个定点突变体的RC进行了光诱导傅里叶变换红外(FTIR)光谱分析。在pH 7条件下,通过单次饱和闪光激发,获得了天然RC以及含有单个位点突变(L212位为Gln,即EQ L212;L213位为Asn,即DN L213;或L210位为Asn,即DN L210)或双位点突变(L212位为Gln且L213位为Asn,即EQ L212 + DN L213)的RC突变体的FTIR QB-/QB光谱。通过结合定点诱变和1H/2H同位素交换的影响,分析了特定羧基侧链的质子化/去质子化的红外波段归属。在Wt、DN L213和DN L210的QB-/QB光谱中,在1728 cm-1处观察到一个正峰,而在突变体EQ L212和EQ L212 + DN L213中则没有。1728 cm-1峰的强度在2H2O中显著降低,并且在1717 +/- 1 cm-1处出现了一个新特征。此外,1728 cm-1峰的幅度在天然和DN L210的RC中相似,但在DN L213中有所增加。该峰归因于Glu L212的部分质子摄取,在天然和DN L210的RC中估计为0.3 - 0.4 H+/QB-,在DN L213的RC中为0.5 - 0.6 H+/QB-。相比之下,FTIR QB-/QB光谱没有显示出QB-形成时Asp L213的质子化或环境变化的证据。DN L213的RC中Glu L212质子化增加是由于带负电荷的Asp L213缺失导致Glu L212的pKa值降低。1732(+)/1740(-)cm-1处受1H/2H交换影响的小差异信号的一部分暂定为质子化Asp L210的环境变化。1685 cm-1处的负信号被认为是由Glu L212的酰胺I羰基模式的吸收变化引起的。(摘要截短为400字)