Werner Erin, Roe Frank, Bugnicourt Amandine, Franklin Michael J, Heydorn Arne, Molin Søren, Pitts Betsey, Stewart Philip S
Center for Biofilm Engineering, Montana State University-Bozeman, Bozeman, MT 59717-3980, USA.
Appl Environ Microbiol. 2004 Oct;70(10):6188-96. doi: 10.1128/AEM.70.10.6188-6196.2004.
In this study, stratified patterns of protein synthesis and growth were demonstrated in Pseudomonas aeruginosa biofilms. Spatial patterns of protein synthetic activity inside biofilms were characterized by the use of two green fluorescent protein (GFP) reporter gene constructs. One construct carried an isopropyl-beta-d-thiogalactopyranoside (IPTG)-inducible gfpmut2 gene encoding a stable GFP. The second construct carried a GFP derivative, gfp-AGA, encoding an unstable GFP under the control of the growth-rate-dependent rrnBp(1) promoter. Both GFP reporters indicated that active protein synthesis was restricted to a narrow band in the part of the biofilm adjacent to the source of oxygen. The zone of active GFP expression was approximately 60 microm wide in colony biofilms and 30 microm wide in flow cell biofilms. The region of the biofilm in which cells were capable of elongation was mapped by treating colony biofilms with carbenicillin, which blocks cell division, and then measuring individual cell lengths by transmission electron microscopy. Cell elongation was localized at the air interface of the biofilm. The heterogeneous anabolic patterns measured inside these biofilms were likely a result of oxygen limitation in the biofilm. Oxygen microelectrode measurements showed that oxygen only penetrated approximately 50 microm into the biofilm. P. aeruginosa was incapable of anaerobic growth in the medium used for this investigation. These results show that while mature P. aeruginosa biofilms contain active, growing cells, they can also harbor large numbers of cells that are inactive and not growing.
在本研究中,证明了铜绿假单胞菌生物膜中蛋白质合成和生长的分层模式。通过使用两种绿色荧光蛋白(GFP)报告基因构建体来表征生物膜内蛋白质合成活性的空间模式。一种构建体携带异丙基-β-D-硫代半乳糖苷(IPTG)诱导型gfpmut2基因,其编码一种稳定的GFP。第二种构建体携带一种GFP衍生物gfp-AGA,其在依赖生长速率的rrnBp(1)启动子的控制下编码一种不稳定的GFP。两种GFP报告基因均表明,活跃的蛋白质合成仅限于生物膜中与氧气源相邻部分的一条窄带。在菌落生物膜中,活跃的GFP表达区域约为60微米宽,在流动细胞生物膜中为30微米宽。通过用羧苄青霉素处理菌落生物膜来绘制生物膜中细胞能够伸长的区域,羧苄青霉素可阻断细胞分裂,然后通过透射电子显微镜测量单个细胞的长度。细胞伸长位于生物膜的空气界面处。在这些生物膜内测得的异质合成代谢模式可能是生物膜中氧气限制的结果。氧微电极测量表明,氧气仅渗透到生物膜中约50微米的深度。在本研究使用的培养基中,铜绿假单胞菌无法进行厌氧生长。这些结果表明,虽然成熟的铜绿假单胞菌生物膜包含活跃生长的细胞,但它们也可能含有大量不活跃且不生长的细胞。