Fidopiastis Pat M, Rader Bethany A, Gerling David G, Gutierrez Nestor A, Watkins Katherine H, Frey Michelle West, Nyholm Spencer V, Whistler Cheryl A
Biological Sciences Department, California Polytechnic University, San Luis Obispo, California, USA.
J Bacteriol. 2012 Aug;194(15):3995-4002. doi: 10.1128/JB.00108-12. Epub 2012 May 25.
Vibrio fischeri cells are the sole colonists of a specialized light organ in the mantle cavity of the sepiolid squid Euprymna scolopes. The process begins when the bacteria aggregate in mucus secretions outside the light organ. The cells eventually leave the aggregate, enter the light organ, and encounter a rich supply of peptides. The need to dissociate from mucus and presumably utilize peptides led us to hypothesize that protease activity is integral to the colonization process. Protease activity associated with whole cells of Vibrio fischeri strain ES114 was identified as the product of a putative cell membrane-associated aminopeptidase (PepN). To characterize this activity, the aminopeptidase was cloned, overexpressed, and purified. Initial steady-state kinetic studies revealed that the aminopeptidase has broad activity, with a preference for basic and hydrophobic side chains and k(cat) and K(m) values that are lower and smaller, respectively, than those of Escherichia coli PepN. A V. fischeri mutant unable to produce PepN is significantly delayed in its ability to colonize squid within the first 12 h, but eventually it establishes a wild-type colonization level. Likewise, in competition with the wild type for colonization, the mutant is outcompeted at 12 h postinoculation but then competes evenly by 24 h. Also, the PepN-deficient strain fails to achieve wild-type levels of cells in aggregates, suggesting an explanation for the initial colonization delay. This study provides a foundation for more studies on PepN expression, localization, and role in the early stages of squid colonization.
费氏弧菌细胞是乌贼(Euprymna scolopes)外套腔中一个特殊发光器官的唯一定殖菌。这个过程始于细菌在发光器官外的黏液分泌物中聚集。细胞最终离开聚集体,进入发光器官,并遇到丰富的肽供应。从黏液中解离并利用肽的需求使我们推测蛋白酶活性是定殖过程不可或缺的一部分。与费氏弧菌菌株ES114全细胞相关的蛋白酶活性被鉴定为一种假定的细胞膜相关氨肽酶(PepN)的产物。为了表征这种活性,对氨肽酶进行了克隆、过表达和纯化。初步的稳态动力学研究表明,该氨肽酶具有广泛的活性,偏好碱性和疏水性侧链,其催化常数(k(cat))和米氏常数(K(m))分别低于大肠杆菌的PepN。一个无法产生PepN的费氏弧菌突变体在最初12小时内定殖乌贼的能力显著延迟,但最终它建立了野生型的定殖水平。同样,在与野生型竞争定殖时,该突变体在接种后12小时被淘汰,但到24小时时竞争相当。此外,缺乏PepN的菌株在聚集体中无法达到野生型的细胞水平,这为最初的定殖延迟提供了解释。这项研究为进一步研究PepN在乌贼定殖早期阶段的表达、定位和作用奠定了基础。