Pinta Violaine, Picaud Martine, Reiss-Husson Françoise, Astier Chantal
Laboratoire de Génétique des Bactéries Photosynthétiques, Centre de Génétique Moléculaire, UPR2167 associée à l'Université Pierre-et-Marie-Curie, CNRS, 91198 Gif-sur-Yvette Cedex, France.
J Bacteriol. 2002 Feb;184(3):746-53. doi: 10.1128/JB.184.3.746-753.2002.
This study describes the characterization of orf358, an open reading frame of previously unidentified function, in the purple bacterium Rubrivivax gelatinosus. A strain in which orf358 was disrupted exhibited a phenotype similar to the wild type under photosynthesis or low-aeration respiratory growth conditions. In contrast, under highly aerated respiratory growth conditions, the wild type still produced bacteriochlorophyll a (Bchl a), while the disrupted strain accumulated a compound that had the same absorption and fluorescence emission spectra as Mg-protoporphyrin but was less polar, suggesting that it was Mg-protoporphyrin monomethylester (MgPMe). These data indicated a blockage in Bchl a synthesis at the oxidative cyclization stage and implied the coexistence of two different mechanisms for MgPMe cyclization in R. gelatinosus, an anaerobic mechanism active under photosynthesis or low oxygenation and an aerobic mechanism active under high-oxygenation growth conditions. Based on these results as well as on sequence analysis indicating the presence of conserved putative binuclear-iron-cluster binding motifs, the designation of orf358 as acsF (for aerobic cyclization system Fe-containing subunit) is proposed. Several homologs of AcsF were found in a wide range of photosynthetic organisms, including Chlamydonomas reinhardtii Crd1 and Pharbitis nil PNZIP, suggesting that this aerobic oxidative cyclization mechanism is conserved from bacteria to plants.
本研究描述了紫色细菌嗜胶红游动菌中orf358(一个功能此前未明的开放阅读框)的特征。在光合作用或低通气量呼吸生长条件下,orf358被破坏的菌株表现出与野生型相似的表型。相反,在高通气量呼吸生长条件下,野生型仍能产生细菌叶绿素a(Bchl a),而被破坏的菌株积累了一种化合物,其吸收光谱和荧光发射光谱与镁原卟啉相同,但极性较小,表明它是镁原卟啉单甲酯(MgPMe)。这些数据表明在Bchl a合成的氧化环化阶段出现了阻断,并暗示在嗜胶红游动菌中存在两种不同的MgPMe环化机制,一种是在光合作用或低氧条件下活跃的厌氧机制,另一种是在高氧生长条件下活跃的需氧机制。基于这些结果以及序列分析表明存在保守的假定双核铁簇结合基序,建议将orf358命名为acsF(用于需氧环化系统含铁亚基)。在广泛的光合生物中发现了几种AcsF的同源物,包括莱茵衣藻Crd1和牵牛PNZIP,这表明这种需氧氧化环化机制从细菌到植物都是保守的。