Mullins P H, Gürtler H, Wellington E M
Department of Biological Sciences, University of Warwick, Coventry, UK.
Microbiology (Reading). 1995 Sep;141 ( Pt 9):2149-56. doi: 10.1099/13500872-141-9-2149.
A polyclonal antibody raised to Streptosporangium fragile spores reacted strongly and specifically with the immunizing strain and to a number of related species of Streptosporangium, as determined by dot immunoblotting. An indirect immunomagnetic capture method was developed for the recovery of the target organism from sterile and non-sterile soil, using sheep anti-rabbit M-280 Dynabeads. The effects of different soil blocking agents, antibody labelling concentrations and spore/Dynabead capture times on the recovery of S. fragile spores were investigated. Pre-blocking of antibody binding sites within the soil, with either 2% partially hydrolysed gelatin or 10% skimmed milk, was essential prior to immunomagnetic capture. Increasing the capture time from 15 to 60 min did not affect spore recovery; however, a 10-fold decline in the magnetic bead concentration did result in a significantly lower recovery of spores from soil. S. fragile was selectively enriched (1:190-fold) when present as a mixed population with Arthrobacter oxydans in sterile soil. The indirect immunomagnetic capture method was used to selectively recover S. fragile spores seeded into non-sterile soil, although some background binding of non-target bacteria was noted. The target was successfully recovered from a sterile soil microcosm after 14 d incubation and the capture rate was increased by the inclusion of an initial soil dispersion and biomass concentration procedure, using the ion-exchange resin Chelex 100.
通过斑点免疫印迹法测定,针对脆弱链霉菌孢子产生的多克隆抗体与免疫菌株以及一些相关的链霉菌物种发生强烈且特异性的反应。利用羊抗兔M-280磁珠开发了一种间接免疫磁捕获方法,用于从无菌和非无菌土壤中回收目标生物体。研究了不同土壤封闭剂、抗体标记浓度和孢子/磁珠捕获时间对脆弱链霉菌孢子回收的影响。在免疫磁捕获之前,用2%部分水解明胶或10%脱脂牛奶对土壤中的抗体结合位点进行预封闭至关重要。将捕获时间从15分钟增加到60分钟并不影响孢子回收;然而,磁珠浓度降低10倍确实导致从土壤中回收的孢子显著减少。当脆弱链霉菌与氧化节杆菌在无菌土壤中作为混合菌群存在时,可被选择性富集(1:190倍)。间接免疫磁捕获方法用于选择性回收接种到非无菌土壤中的脆弱链霉菌孢子,不过注意到有一些非目标细菌的背景结合。在无菌土壤微宇宙中培养14天后成功回收了目标物,并且通过使用离子交换树脂Chelex 100进行初始土壤分散和生物量浓缩程序,捕获率有所提高。