Deshpande M, Calenoff E, Daniels L
Department of Microbiology, University of Iowa, Iowa City 52242, USA.
Appl Environ Microbiol. 1995 Jun;61(6):2431-5. doi: 10.1128/aem.61.6.2431-2435.1995.
We developed procedures for large-scale cultivation of Helicobacter pylori in flasks and fermentors. Flasks incubated closed under a microaerophilic gas phase with a cotton plug covered by a plastic bag, followed by removal of the bag after 8 h, gave excellent growth. Growth in a 10-liter fermentor led to excessive foaming if the medium was sparged with gas; silicone- or polyglycol-based antifoaming agents were severely inhibitory. Use of fermentor surface gassing, first with a microaerophilic 6% oxygen gas mixture, then with air, and then with 95% oxygen, allowed the culture to grow to an A600 of 2.5 in < 24 h. This method was modified for scale-up to a 100-liter fermentor.
我们开发了在烧瓶和发酵罐中大规模培养幽门螺杆菌的程序。在微需氧气相条件下,用塑料袋覆盖的棉塞封闭培养烧瓶,8小时后取出塑料袋,可实现良好生长。如果向培养基中鼓入气体,在10升发酵罐中培养会导致过度起泡;基于硅酮或聚乙二醇的消泡剂具有严重抑制作用。使用发酵罐表面通气法,先通入含6%氧气的微需氧气体混合物,再通入空气,然后通入95%氧气,可使培养物在不到24小时内生长至A600为2.5。此方法经改进后可扩大至100升发酵罐。