Ångström Laboratories, Department of Photochemistry and Molecular Science, Uppsala University, Uppsala, Sweden.
FEMS Microbiol Lett. 2011 Mar;316(2):152-9. doi: 10.1111/j.1574-6968.2010.02206.x. Epub 2011 Jan 24.
All diazotrophic filamentous cyanobacteria contain an uptake hydrogenase that is involved in the reoxidation of H(2) produced during N(2) -fixation. In Nostoc punctiforme ATCC 29133, N(2) -fixation takes place in the microaerobic heterocysts, catalysed by a nitrogenase. Although the function of the uptake hydrogenase may be closely connected to that of nitrogenase, the localization in cyanobacteria has been under debate. Moreover, the subcellular localization is not understood. To investigate the cellular and subcellular localization of the uptake hydrogenase in N. punctiforme, a reporter construct consisting of the green fluorescent protein (GFP) translationally fused to HupS, within the complete hupSL operon, was constructed and transferred into N. punctiforme on a self-replicative vector by electroporation. Expression of the complete HupS-GFP fusion protein was confirmed by Western blotting using GFP antibodies. The N. punctiforme culture expressing HupS-GFP was examined using laser scanning confocal microscopy, and fluorescence was exclusively detected in the heterocysts. Furthermore, the fluorescence in mature heterocysts was localized to several small or fewer large clusters, which indicates a specificity of the subcellular localization of the uptake hydrogenase.
所有固氮丝状蓝藻都含有一种摄取氢化酶,它参与了 N2 固定过程中产生的 H2 的再氧化。在鱼腥藻 ATCC 29133 中,N2 固定发生在微氧异形胞中,由固氮酶催化。尽管摄取氢化酶的功能可能与固氮酶密切相关,但它在蓝藻中的定位一直存在争议。此外,其亚细胞定位尚不清楚。为了研究鱼腥藻中摄取氢化酶的细胞和亚细胞定位,构建了一个由 GFP 翻译融合到 HupS 内的报告基因构建体,位于完整的 hupSL 操纵子中,并通过电穿孔将其转移到鱼腥藻的自我复制载体上。使用 GFP 抗体通过 Western blot 验证了完整的 HupS-GFP 融合蛋白的表达。使用激光扫描共聚焦显微镜检查表达 HupS-GFP 的鱼腥藻培养物,荧光仅在异形胞中检测到。此外,成熟异形胞中的荧光定位于几个小簇或较少的大簇,这表明摄取氢化酶的亚细胞定位具有特异性。