食品科学 ›› 2018, Vol. 39 ›› Issue (22): 305-311.doi: 10.7506/spkx1002-6630-201822046

• 安全检测 • 上一篇    下一篇

基于基因测序鱼露发酵橘青霉YL-1鉴定及安全性评价

宋佳佳1,古汶玉1,林昌浩1,张晓勇2,甘忠宏1,谢莉1,高向阳1,*   

  1. (1.华南农业大学食品学院,广东?广州 514642;2.华南农业大学海洋学院,广东?广州 514642)
  • 出版日期:2018-11-25 发布日期:2018-11-21
  • 基金资助:
    广东省公益研究与能力建设项目(2016B020204004)

Molecular Identification and Safety Evaluation of Penicillium citrinum YL-1 from Fish Sauce Based on Fungal Genomic Sequencing

SONG Jiajia1, GU Wenyu1, LIN Changhao1, ZHANG Xiaoyong2, GAN Zhonghong1, XIE Li1, GAO Xiangyang1,*   

  1. (1. College of Food Science, South China Agricultural University, Guangzhou 514642, China; 2. College of Marine Sciences, South China Agricultural University, Guangzhou 514642, China)
  • Online:2018-11-25 Published:2018-11-21

摘要: 目的:为弥补传统方法在检测菌株产毒素上的不足,用基因组方法分析橘青霉YL-1(Penicillium citrinum YL-1,P. citrinum YL-1)物质生物合成途径及关键基因,以此评价P. citrinum YL-1在鱼露发酵生产过程中的安全性。方法:应用ITS基因测序鉴定菌株,利用Illumina平台Hiseq测序技术对菌株YL-1进行基因组survey测序,通过生物信息分析产青霉毒素、黄曲霉毒素及典型丝状真菌毒素的非核糖体多肽合成代谢、聚合酮酶代谢、聚合酮酶-非核糖体多肽联合代谢、萜类化合物代谢和氨基酸相关代谢途径及基因,考察菌株YL-1产真菌毒素能力,判断其是否存在产真菌毒素的潜在危害。结果:ITS鉴定菌株YL-1与P. citrinum同源性99%,survey测序结果表明P. citrinum YL-1全基因组大小为31.92?Mb,GC为46.27%。利用Maker2基因预测技术得到预测基因11?980?个。其中,被KOG注释基因5?417?个,被COG注释基因4?946?个;比对KEGG数据库被注释通路323?条,注释基因3?525?个。代谢分析表明,注释到可能产真菌毒素相关的代谢途径有5?条,仅注释到1?种产黄曲霉毒素代谢途径的同源基因Afld及其他5?种相关基因,但并未注释到其完整代谢途径。结论:ITS基因测序鉴定菌株YL-1为P. citrinum,P. citrinum YL-1基因注释存在1 种产黄曲霉毒素的同源基因及其他5?种相关基因,虽不存在完整代谢链,但P. citrinum YL-1运用于鱼露及相关产品的发酵安全性仍值得进一步考察。

关键词: 橘青霉YL-1, 真菌毒素, 安全性, 基因测序

Abstract: Objective: In order to overcome the deficiency of the traditional method to toxin-producing fungi, the toxin biosynthetic pathways and related key genes in Penicillium citrinum YL-1 were investigated by genomics to evaluate the safety of P. citrinum YL-1 during fish sauce fermentation. Methods: The strain was identified by internal transcribed spacer (ITS) sequencing. Genome survey of strain YL-1 was performed using the Illumina Hiseq platform. The key synthetic pathways and genes involved in the synthesis of Penicillium toxin and aflatoxin, as well as mycotoxin metabolism in which strain YL-1 may be involved were analyzed. The metabolic pathways of non-ribosomal peptide synthetase (NRPS), polyketide synthase (PKS), PKS-NRPS, terpenoid and amino acids and related genes were analyzed by bioinformatics tools. The mycotoxin-producing ability of YL-1 was determined to evaluate whether there was a potential hazard of mycotoxin. Results: Strain YL-1 was identified as P. citrinum with a 99% similarity. The genome of P. citrinum YL-1 was 31.92 Mb in length with GC content of 46.27%. A total of 11 980 genes were predicted using Maker2 sequencing by homology analysis, including 5 417 eukaryotic genes and 4 946 prokaryotic genes annotated in eukaryote clusters of orthologous groups (KOG) and cluster of orthologous groups of proteins (COG) databases, respectively. Kyoto Encyclopaedia of Genes and Genomes (KEGG) analysis was used to assign 3 525 genes to 323 pathways. Five metabolic pathways related to the biosynthesis of mycotoxins were annotated in P. citrinum YL-1, including only one homologous gene (Afld) involved in the metabolic pathway of aflatoxin and five other related genes. However, no complete metabolic pathway was annotated. Conclusion: Despite the above findings, further studies should be done to evaluate the safety of P. citrinum YL-1 in fish sauce and other related products.

Key words: Penicillium citrinum YL-1, mycotoxins, safety, genomic sequence

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