科学技术与工程
科學技術與工程
과학기술여공정
Science Technology and Engineering
2015年
32期
143-146
,共4页
刘艳超%郝文利%宿庄%高玉敏
劉豔超%郝文利%宿莊%高玉敏
류염초%학문리%숙장%고옥민
宏基因组DNA%自来水%菌落总数%相关性%检测方法
宏基因組DNA%自來水%菌落總數%相關性%檢測方法
굉기인조DNA%자래수%균락총수%상관성%검측방법
metagenomic DNA%drinking water%total number of bacterial colonies%correlation detection method
分析自来水中细菌宏基因组DNA浓度与细菌菌落总数之间的相关性,探索新的自来水细菌菌落总数检测方法。采用国标法检测自来水中的细菌菌落总数约为(165±5) CFU/mL,高于国标限值(100 CFU/mL)。通过计算得出,检测600 mL本实验水样中的细菌菌落总数相当于检测1000 mL(1 L)100 CFU/mL的自来水。首先将600 mL及低于和高于该体积不同体积梯度的自来水经滤膜过滤收集菌体;然后使用细菌基因组提取试剂盒提取滤膜上的细菌宏基因组DNA,电泳分析提取的宏基因组质量;最后检测各个体积自来水宏基因组DNA浓度,根据检测结果分析自来水中宏基因组DNA含量与细菌菌落总数之间的相关性。提取的自来水宏基因组DNA主条带清晰,可以进行基因组DNA含量测定分析;自来水中细菌宏基因组DNA浓度与细菌菌落总数之间呈正相关的线性关系。建立一种通过检测自来水中细菌宏基因组DNA浓度来反映细菌菌落总数的检测方法,检测灵敏度可达7 CFU/mL,且省时、重复性好。
分析自來水中細菌宏基因組DNA濃度與細菌菌落總數之間的相關性,探索新的自來水細菌菌落總數檢測方法。採用國標法檢測自來水中的細菌菌落總數約為(165±5) CFU/mL,高于國標限值(100 CFU/mL)。通過計算得齣,檢測600 mL本實驗水樣中的細菌菌落總數相噹于檢測1000 mL(1 L)100 CFU/mL的自來水。首先將600 mL及低于和高于該體積不同體積梯度的自來水經濾膜過濾收集菌體;然後使用細菌基因組提取試劑盒提取濾膜上的細菌宏基因組DNA,電泳分析提取的宏基因組質量;最後檢測各箇體積自來水宏基因組DNA濃度,根據檢測結果分析自來水中宏基因組DNA含量與細菌菌落總數之間的相關性。提取的自來水宏基因組DNA主條帶清晰,可以進行基因組DNA含量測定分析;自來水中細菌宏基因組DNA濃度與細菌菌落總數之間呈正相關的線性關繫。建立一種通過檢測自來水中細菌宏基因組DNA濃度來反映細菌菌落總數的檢測方法,檢測靈敏度可達7 CFU/mL,且省時、重複性好。
분석자래수중세균굉기인조DNA농도여세균균락총수지간적상관성,탐색신적자래수세균균락총수검측방법。채용국표법검측자래수중적세균균락총수약위(165±5) CFU/mL,고우국표한치(100 CFU/mL)。통과계산득출,검측600 mL본실험수양중적세균균락총수상당우검측1000 mL(1 L)100 CFU/mL적자래수。수선장600 mL급저우화고우해체적불동체적제도적자래수경려막과려수집균체;연후사용세균기인조제취시제합제취려막상적세균굉기인조DNA,전영분석제취적굉기인조질량;최후검측각개체적자래수굉기인조DNA농도,근거검측결과분석자래수중굉기인조DNA함량여세균균락총수지간적상관성。제취적자래수굉기인조DNA주조대청석,가이진행기인조DNA함량측정분석;자래수중세균굉기인조DNA농도여세균균락총수지간정정상관적선성관계。건립일충통과검측자래수중세균굉기인조DNA농도래반영세균균락총수적검측방법,검측령민도가체7 CFU/mL,차성시、중복성호。
Through analyzing the correlation between the bacterial metagenomic DNA concentration and the total count of bacterial colonies in drinking water, we explore a new method for the detection of total number of bacterial colonies in drinking water.The total number of bacteria colonies in the water from our lab was detected by a tradi-tional technology, and it was about ( 165 ±5 ) CFU/mL, which is higher than 100 CFU/mL that is the security boundary value which was made by Chinese health department in 2006.To limit the total number of bacterial colo-nies within 100 CFU/mL,the volume of the detection sample must below 600 mL.Firstly, the sample with different volumes higher or lower than 600 mL is treated with microfiltration; Secondly, extract the bacterial metagenomic DNA of filter membrane by Bacterial Genome Extraction Kit;Thirdly, analyze the DNA extracted by agarose gel e-lectrophoresis;Fourthly, determine the concentration of DNA extracted.Finally, analyze the correlation between the bacterial metagenomic DNA concentration and the total count of bacterial colonies in drinking water according to the experimental results.The bacterial metagenomic DNA extracted from different volumes of drinking water pro-duce clear bands, and the DNA contents are enough for further analysis;the correlation between the bacterial met-agenomic DNA concentration and the total count of bacterial colonies in drinking water is positive and linear.To es-tablish a new method for detection of total number of bacterial colonies by analyzing the bacterial metagenomic DNA concentration in drinking water, the detection sensitivity can reach 7 CFU/mL, and the method is time-saving and with good repetitiveness.