Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99352, USA.
Department of Translational Medicine and Physiology, Elson S. Floyd College of Medicine, Washington State University, Spokane, WA 99202, USA.
Org Biomol Chem. 2023 May 17;21(19):4028-4038. doi: 10.1039/d2ob02257e.
Diurnal rhythmicity of cellular function is key to survival for most organisms on Earth. Many circadian functions are driven by the brain, but regulation of a separate set of peripheral rhythms remains poorly understood. The gut microbiome is a potential candidate for regulation of host peripheral rhythms, and this study sought to specifically examine the process of microbial bile salt biotransformation. To enable this work, an assay for bile salt hydrolase (BSH) that could work with small quantities of stool samples was necessary. Using a turn-on fluorescence probe, we developed a rapid and inexpensive assay to detect BSH enzyme activity with concentrations as low as 6-25 μM, which is considerably more robust than prior approaches. We successfully applied this rhodamine-based assay to detect BSH activity in a wide range of biological samples such as recombinant protein, whole cells, fecal samples, and gut lumen content from mice. We were able to detect significant BSH activity in small amounts of mouse fecal/gut content (20-50 mg) within 2 h, which illustrates its potential for use in various biological/clinical applications. Using this assay, we investigated the diurnal fluctuations of BSH activity in the large intestine of mice. By using time restricted feeding conditions, we provided direct evidence of 24 h rhythmicity in microbiome BSH activity levels and showed that this rhythmicity is influenced by feeding patterns. Our novel function-centric approach has potential to aid in the discovery of therapeutic, diet, or lifestyle interventions for correction of circadian perturbations linked to bile metabolism.
细胞功能的昼夜节律性是地球上大多数生物生存的关键。许多昼夜节律功能受大脑驱动,但对另一套外周节律的调节仍知之甚少。肠道微生物组是调节宿主外周节律的潜在候选者,本研究旨在专门研究微生物胆汁盐转化的过程。为了实现这一目标,需要开发一种能够处理少量粪便样本的胆汁盐水解酶(BSH)检测方法。我们使用一种开启型荧光探针,开发了一种快速且廉价的检测 BSH 酶活性的方法,其检测浓度低至 6-25 μM,比之前的方法更具稳健性。我们成功地将这种基于罗丹明的检测方法应用于检测生物样本中的 BSH 活性,包括重组蛋白、全细胞、粪便样本和来自小鼠的肠道腔内容物。我们能够在 2 小时内从小鼠粪便/肠道内容物(20-50mg)中检测到显著的 BSH 活性,这说明了它在各种生物/临床应用中的潜力。使用该检测方法,我们研究了小鼠大肠中 BSH 活性的昼夜波动。通过采用限时喂养条件,我们提供了微生物 BSH 活性水平 24 小时节律性的直接证据,并表明这种节律性受喂养模式的影响。我们的新功能中心方法有可能有助于发现治疗、饮食或生活方式干预措施,以纠正与胆汁代谢相关的昼夜节律紊乱。