Kyndt J A, Hurley J K, Devreese B, Meyer T E, Cusanovich M A, Tollin G, Van Beeumen J J
Laboratory of Protein Biochemistry and Protein Engineering, University of Gent, Ledeganckstraat 35, 9000 Gent, Belgium.
Biochemistry. 2004 Feb 24;43(7):1809-20. doi: 10.1021/bi035789f.
A gene for photoactive yellow protein (PYP) was previously cloned from Rhodobacter capsulatus (Rc), and we have now found it to be associated with genes for gas vesicle formation in the recently completed genome sequence. However, the PYP had not been characterized as a protein. We have now produced the recombinant RcPYP in Escherichia coli as a glutathione-S-transferase (GST) fusion protein, along with the biosynthetic enzymes, resulting in the formation of holo-RcPYP following cleavage of the GST tag. The absorption spectrum (with characteristic peaks at 435 and 375 nm) and the photocycle kinetics, initiated by a laser flash at 445 nm, are generally similar to those of Rhodobacter sphaeroides (RsPYP) but are significantly different from those of the prototypic PYP from Halorhodospira halophila (HhPYP), which has a single peak at 446 nm and has slower recovery. RcPYP also is photoactive when excited with near-ultraviolet laser light, but the end point is then above the preflash baseline. This suggests that some of the PYP chromophore is present in the cis-protonated conformation in the resting state. The excess 435 nm form in RcPYP, built up from repetitive 365 nm laser flashes, returns to the preflash baseline with an estimated half-life of 2 h, which is markedly slower than that for the same reaction in RsPYP. Met100 has been reported to facilitate cis-trans isomerization in HhPYP, yet both Rc and RsPYPs have Lys and Gly substitutions at positions 99 and 100 (using HhPYP numbering throughout) and have 100-fold faster recovery kinetics than does HhPYP. However, the G100M and K99Q mutations of RcPYP have virtually no effect on kinetics. Apparently, the RcPYP M100 is in a different conformation, as was recently found for the PYP domain of Rhodocista centenaria Ppr. The cumulative results show that the two Rhodobacter PYPs are clearly distinct from the other species of PYP that have been characterized. These properties also suggest a different functional role, that we postulate to be in regulation of gas vesicle genes, which are known to be light-regulated in other species.
光活性黄色蛋白(PYP)基因先前已从荚膜红细菌(Rc)中克隆出来,而我们现在发现在最近完成的基因组序列中它与气体囊泡形成相关基因相连。然而,PYP此前尚未作为一种蛋白质得到表征。我们现在已在大肠杆菌中表达出重组RcPYP,它是一种谷胱甘肽-S-转移酶(GST)融合蛋白,同时还有生物合成酶,在去除GST标签后形成全酶形式的RcPYP。其吸收光谱(在435和375nm处有特征峰)以及由445nm激光闪光引发后的光循环动力学,总体上与球形红细菌(RsPYP)相似,但与嗜盐嗜盐红螺菌(HhPYP)的原型PYP显著不同,后者在446nm处有单峰且恢复较慢。当用近紫外激光激发时,RcPYP也具有光活性,但终点高于闪光前基线。这表明在静息状态下,部分PYP发色团以顺式质子化构象存在。通过重复365nm激光闪光积累形成的RcPYP中过量的435nm形式,以估计2小时的半衰期回到闪光前基线,这明显慢于RsPYP中相同反应的半衰期。据报道,Met100有助于HhPYP中的顺反异构化,但RcPYP和RsPYP在99和100位(全程采用HhPYP编号)都有赖氨酸和甘氨酸取代,且恢复动力学比HhPYP快100倍。然而,RcPYP的G100M和K99Q突变对动力学几乎没有影响。显然,RcPYP的M100处于不同构象,就像最近在百岁红杆菌Ppr的PYP结构域中发现的那样。累积结果表明,这两种红细菌PYP与已表征的其他PYP物种明显不同。这些特性还暗示了一种不同的功能作用,我们推测其作用是调节气体囊泡基因,已知在其他物种中这些基因受光调节。