摘要
目的建立基于基因水平的产B类伏马菌素黑曲霉菌株的鉴定方法。方法通过聚合酶链反应(polymerase chain reaction,PCR)和反转录-PCR(reverse transcription-PCR,RT-PCR)对产B类伏马菌素黑曲霉基因簇中8个关键基因的DNA和mRNA提取方法、扩增条件等进行优化,并对其表达产物进行分析。结果检测的19株黑曲霉菌株均携带与B类伏马菌素合成相关的8个关键基因的DNA。其中与产毒量相关性较强的基因为fum6、fum14和fum19,但不同产毒水平黑曲霉菌株中8个关键基因的mRNA表达量各异。结论 DNA水平不足以鉴别黑曲霉菌株B类伏马菌素的产毒能力,需要结合mRNA表达水平综合分析。
Objective To develop a method for identification of B-type fumonisin-producing Aspergillus nigerat genetic level. Methods The DNA and mRNA extraction method, conditions fo ramplification of eight key genes of B-type fumonisin-producing gene cluster of Aspergillus niger by polymerase chain reaction (PCR) and reverse transcription-PCR (RT-PCR) were optimized. The expression products were analyzed. Results The DNA of eight key genes related to B-type fumonisin biosynthesis were detected in all 19 strains of Aspergillus niger, fum6, fum14, fi^ml9 were the most predominant genes in Aspergillus niger in association with fumonisin production, but the mRNA expression level of the 8 key genes were different which leaded to different B-type fumonisin produce ability. Conclusion B-type and non-B-type fumonisin-producing Aspergillus nigercould not be distinguished at DNA level. DNA in combination with mRNA expression level was needed to identify B-type fumonisin-producing Aspergillus niger.
出处
《中国食品卫生杂志》
北大核心
2014年第2期105-110,共6页
Chinese Journal of Food Hygiene
基金
国家自然科学基金(81072307)
国家自然科学基金(31301489)
关键词
黑曲霉
B类伏马菌素
产毒基因
菌株鉴定
霉菌毒素
食品安全
Aspergillus niger
B-type fumonisin
toxin producing gene
strain identification
mycotoxin
food safety