Stephen Camille S, LaBelle Edward V, Brantley Susan L, Bond Daniel R
Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania, United States of America.
BioTechnology Institute, University of Minnesota, St. Paul, Minnesota, United States of America.
PLoS One. 2014 Aug 4;9(8):e104336. doi: 10.1371/journal.pone.0104336. eCollection 2014.
When Geobacter sulfurreducens utilizes an electrode as its electron acceptor, cells embed themselves in a conductive biofilm tens of microns thick. While environmental conditions such as pH or redox potential have been shown to change close to the electrode, less is known about the response of G. sulfurreducens to growth in this biofilm environment. To investigate whether respiratory protein abundance varies with distance from the electrode, antibodies against an outer membrane multiheme cytochrome (OmcB) and cytoplasmic acetate kinase (AckA) were used to determine protein localization in slices spanning ∼25 µm-thick G. sulfurreducens biofilms growing on polished electrodes poised at +0.24 V (vs. Standard Hydrogen Electrode). Slices were immunogold labeled post-fixing, imaged via transmission electron microscopy, and digitally reassembled to create continuous images allowing subcellular location and abundance per cell to be quantified across an entire biofilm. OmcB was predominantly localized on cell membranes, and 3.6-fold more OmcB was detected on cells 10-20 µm distant from the electrode surface compared to inner layers (0-10 µm). In contrast, acetate kinase remained constant throughout the biofilm, and was always associated with the cell interior. This method for detecting proteins in intact conductive biofilms supports a model where the utilization of redox proteins changes with depth.
当硫还原地杆菌利用电极作为其电子受体时,细胞会嵌入到几十微米厚的导电生物膜中。虽然已表明诸如pH值或氧化还原电位等环境条件在电极附近会发生变化,但关于硫还原地杆菌在这种生物膜环境中生长的反应却知之甚少。为了研究呼吸蛋白丰度是否随距电极的距离而变化,针对外膜多血红素细胞色素(OmcB)和细胞质乙酸激酶(AckA)的抗体被用于确定在固定于+0.24 V(相对于标准氢电极)的抛光电极上生长的约25 µm厚的硫还原地杆菌生物膜切片中的蛋白质定位。切片在固定后进行免疫金标记,通过透射电子显微镜成像,并进行数字重组以创建连续图像,从而能够对整个生物膜中每个细胞的亚细胞位置和丰度进行量化。OmcB主要定位于细胞膜上,与内层(0 - 10 µm)相比,在距电极表面10 - 20 µm的细胞上检测到的OmcB多3.6倍。相比之下,乙酸激酶在整个生物膜中保持恒定,并且始终与细胞内部相关联。这种在完整导电生物膜中检测蛋白质的方法支持了一种模型,即氧化还原蛋白的利用随深度而变化。