Nairn C A, Cole J A, Patel P V, Parsons N J, Fox J E, Smith H
Department of Microbiology, University of Birmingham, UK.
J Gen Microbiol. 1988 Dec;134(12):3295-306. doi: 10.1099/00221287-134-12-3295.
A low-Mr factor which induces gonococcal resistance to complement-mediated serum killing has been partially purified from lysates of mixed red and buffy coat cells from human blood. The lysates were dialysed against Tris buffer for 24 h at 25 degrees C with the diffusate being continuously recycled through a column of QAE-Sephadex A25. After elution in an NaCl gradient, the active fractions were both desalted and further purified on Sephadex G10. A second fractionation on QAE-Sephadex A25 and desalting with Sephadex G10 preceded further purification by repeated high-pressure liquid chromatography (HPLC) using a DEAE anion exchange column and desalting with Sephadex G10. Less than 500 micrograms of material showing one peak in HPLC was obtained from 1 litre of blood. After NMR had indicated the possible presence of pyrimidine nucleotide, carbohydrate and N-acetyl groups, nanogram quantities of a commercial preparation of cytidine 5'-monophospho-N-acetylneuraminic acid (CMP-NANA) were shown to induce gonococci to serum resistance. The synthetic CMP-NANA also co-eluted with the preparation from blood cells in HPLC, and the two materials were indistinguishable in their patterns of acid and heat lability. Furthermore, the resistance-inducing activity of both materials was inhibited by cytidine monophosphate, which is known to inhibit sialylation reactions by CMP-NANA. It appears therefore that the resistance-inducing factor is CMP-NANA or a closely related compound. If the factor is CMP-NANA, biological activities indicated that the cell lysate from 1 litre of blood contained about 40 micrograms, and the most purified preparation contained only about 1%. With this minute amount in a mixture, the presence of CMP-NANA or a closely related analogue could not be established unequivocally by NMR.
一种可诱导淋球菌对补体介导的血清杀伤产生抗性的低分子量因子已从人血的红细胞和白细胞层混合细胞裂解物中部分纯化出来。将裂解物在25℃下用Tris缓冲液透析24小时,透析液通过QAE-葡聚糖A25柱连续循环。在NaCl梯度洗脱后,活性部分先进行脱盐,然后在葡聚糖G10上进一步纯化。在使用DEAE阴离子交换柱进行重复高压液相色谱(HPLC)进一步纯化并用葡聚糖G10脱盐之前,先在QAE-葡聚糖A25上进行第二次分级分离并用葡聚糖G10脱盐。从1升血液中获得的材料在HPLC中显示一个峰,其含量不到500微克。核磁共振(NMR)表明可能存在嘧啶核苷酸、碳水化合物和N-乙酰基后,已证明纳克量的胞苷5'-单磷酸-N-乙酰神经氨酸(CMP-NANA)商业制剂可诱导淋球菌产生血清抗性。合成的CMP-NANA在HPLC中也与血细胞制备物共洗脱,并且这两种物质在酸和热不稳定性模式上无法区分。此外,两种物质的抗性诱导活性均被胞苷一磷酸抑制,已知胞苷一磷酸可抑制CMP-NANA的唾液酸化反应。因此,抗性诱导因子似乎是CMP-NANA或一种密切相关的化合物。如果该因子是CMP-NANA,生物学活性表明1升血液中的细胞裂解物含有约40微克,而最纯的制剂仅含有约1%。由于混合物中的量极少,通过NMR无法明确确定CMP-NANA或密切相关类似物的存在。