Keire D A, Anton P, Faull K F, Ruth E, Walsh J H, Chew P, Quisimoro D, Territo M, Reeve J R
CURE: Digestive Diseases Research Center, Veterans Affairs Greater Los Angeles Health Care System, Los Angeles, California 90073, USA.
J Biol Chem. 2001 Dec 28;276(52):48847-53. doi: 10.1074/jbc.M109811200. Epub 2001 Oct 24.
The structure of a small-molecule, non-peptide chemotactic factor has been determined from activity purified to apparent homogeneity from Helicobacter pylori supernatants. H. pylori was grown in brucella broth media until one liter of solution had 0.9 absorbance units. The culture was centrifuged, and the bacteria re-suspended in physiological saline and incubated at 37 degrees C for 4 h. A monocyte migration bioassay revealed the presence of a single active chemotactic factor in the supernatant from this incubation. The chemotactic factor was concentrated by solid phase chromatography and purified by reverse phase high pressure liquid chromatography. The factor was shown to be indistinguishable from diethyl phthalate (DEP) on the basis of multiple criteria including nuclear magnetic resonance spectroscopy, electron impact mass spectroscopy, UV visible absorption spectrometry, GC and high pressure liquid chromatography retention times, and chemotactic activity toward monocytes. Control experiments with incubated culture media without detectable bacteria did not yield detectable DEP, suggesting it is bacterially derived. It is not known if the bacteria produce diethyl phthalate de novo or if it is a metabolic product of a precursor molecule present in culture media. DEP produced by H. pylori in addition to DEP present in man-made products may contribute to the high levels of DEP metabolites observed in human urine. DEP represents a new class of chemotactic factor.
已从幽门螺杆菌上清液中纯化至表观同质活性的小分子非肽趋化因子的结构得以确定。幽门螺杆菌在布鲁氏菌肉汤培养基中培养,直至一升溶液的吸光度为0.9个单位。培养物离心后,细菌重悬于生理盐水中,并在37℃孵育4小时。单核细胞迁移生物测定显示该孵育上清液中存在单一活性趋化因子。趋化因子通过固相色谱浓缩,并通过反相高压液相色谱纯化。基于包括核磁共振光谱、电子轰击质谱、紫外可见吸收光谱、气相色谱和高压液相色谱保留时间以及对单核细胞的趋化活性等多项标准,该因子被证明与邻苯二甲酸二乙酯(DEP)无法区分。对无可检测细菌的孵育培养基进行的对照实验未产生可检测到的DEP,表明其源自细菌。尚不清楚细菌是从头合成邻苯二甲酸二乙酯,还是它是培养基中存在的前体分子的代谢产物。幽门螺杆菌产生的DEP以及人造产品中存在的DEP可能导致在人类尿液中观察到的高水平DEP代谢物。DEP代表了一类新的趋化因子。