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普洱茶中真菌种群的分离与分子鉴定

  • 赵振军 ,
  • 童华荣 ,
  • 周黎 ,
  • 刘勤晋
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  • 1. 西南大学园艺园林学院,重庆400716;
    2. 西南大学食品学院,重庆 400716
赵振军(1976— ),博士研究生,主要从事普洱茶安全与功能研究。

收稿日期: 2009-07-07

  修回日期: 2009-09-04

  网络出版日期: 2019-09-09

基金资助

普洱茶关键技术研究(2007YNCXB-01-01)

Isolation and Molecular Identification of Fungal Colonization of Pu-erh Tea

  • ZHAO Zhen-jun ,
  • TONG Hua-rong ,
  • ZHOU Li ,
  • LIU Qin-jin
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  • 1. College of Horticulture and Landscape Architecture, Southwest University, Chongqing 400716, China;
    2. College of Food Science, Southwest University, Chongqing 400716, China

Received date: 2009-07-07

  Revised date: 2009-09-04

  Online published: 2019-09-09

摘要

采用平板稀释法以孟加拉红(DRBC)和18%的甘油琼脂(DG18)两种培养基对60个普洱茶样品中的真菌种群进行了分离,种群分离结果显示:样品中真菌种群数量变化值范围为1.6×103~1.16×105 cfu/g;应用分子生物学的手段,对分离到的71株真菌做了分子鉴定,鉴定结果表明:这些真菌分别属于19个属,40个种,主要是曲霉属13种,青霉属7种,其他属20种。数量上占优势的真菌种群是酵母和曲霉属的不同种。这些真菌的安全性有待进一步评估。

本文引用格式

赵振军 , 童华荣 , 周黎 , 刘勤晋 . 普洱茶中真菌种群的分离与分子鉴定[J]. 茶叶科学, 2009 , 29(6) : 436 -442 . DOI: 10.13305/j.cnki.jts.2009.6.06

Abstract

The fungal colonization was investigated from 60 representative samples by using the method of dilution plating on the medium of Dichloran Rose-Bengal Chloramphenicol Agar (DRBC) and dichloran 18% glycerol (DG18) agar. The results of the survey showed that the fungal colonization ranged from 1.6×103 to 1.16×105 cfu/g, and 71 isolates were identified by means of sequencing the rDNA fragments, which belong to 40 species of 19 genera, including 13 species of Aspergillus and 7 species of Penicillium, and 20 species of other genera. The predominant fungi in number were yeasts and different species of the genus Aspergillus. Further evaluation on the safety of these fungi isolated from Pu-erh tea products is needed.

参考文献

[1] Chiang C T, Weng M.S, Lin S A, et al. Pu-erh tea supplementation suppresses fatty acid synthase expression in the rat liver through down regulating Akt and JNK signalings as demonstrated in human hepatoma HepG2 cells[J]. Oncology Research, 2006, 16(3): 119~128.
[2] Duh P D, Yen G C, Yen W J, et al. Effects of Pu-erh tea on oxidative damage and nitric oxide scavenging[J]. Journal of Agricultural and Food Chemistry, 2004(52): 8169~8176.
[3] Jie G.L, Lin Z, Zhang L.Z, et al. Free radical scavenging effect of Pu-erh tea extracts and their protective effect on oxidative damage in human fibroblast cells[J]. Journal of Agricultural and Food Chemistry, 2006, 54(21): 8058~8064.
[4] Kuo K L, Weng M S, Chiang C T, et al. Comparative studies on the hypolipidemic and growth suppressive effects of oolong, black, pu-erh, and green tea leaves in rats[J]. Journal of Agricultural and Food Chemistry, 2005, 53(2): 480~489.
[5] 刘勤晋, 周才琼, 许鸿亮, 等. 普洱茶的渥堆作用[J]. 茶叶科学, 1986, 6(2): 55~56.
[6] 何国藩, 林月蝉, 徐祥福. 广东普洱茶渥堆中细胞组织的显微变化及微生物分析[J]. 茶叶科学, 1987, 7(2): 54~57.
[7] 周红杰, 李家华, 赵龙飞, 等. 渥堆过程中主要微生物对云南普洱茶品质形成的研究[J]. 茶叶科学, 2004, 24(3): 212~218.
[8] Pitt J I, Hocking A D.Fungi and Food Spoilage (2nd ed.)[M]. Blackie Academic & Professional, London, 1997: 307~309.
[9] 朱衡, 瞿峰, 朱立煌. 利用氯化苄提取适于分子生物学分析的真菌DNA[J]. 真菌学报, 1994, 13(1): 34~40.
[10] Guo L D, Hyde K D, Liew E.C.Y. Detection and taxonomic placement of endophytic fungi within frond tissues of Livistona chinensis based on rDNA sequences[J]. Molecular Phylogenetics and Evolution, 2001(20): 1~13.
[11] 吴琦, 王红宁, 刘世贵. 三种黑曲霉细胞基因组DNA提取方法的比较[J]. 生物技术, 13(6): 30~31.
[12] 仓道平, 温琼英. 茯砖茶发酵中优势菌与有害菌类的分离鉴定[J]. 茶叶通讯, 1981(2): 12~14.
[13] 温琼英. 茯砖茶中主要微生物的研究[J]. 茶叶通讯, 1986(4): 19~21.
[14] 齐祖同, 孙曾美. 茯砖茶中优势菌群的鉴定[J]. 真菌学报, 1990, 9(3): 176~179
[15] 陈可可, 朱宏涛, 王东, 等. 普洱熟茶后发酵加工过程中曲霉菌的分离和鉴定[J]. 云南植物研究, 2006, 28(2): 123~126.
[16] A Al Musallam.Revision of the black Aspergillus species[D]. Utrecht: The Netherlands; University of Utrecht, 1980.
[17] Pitt J I, Hocking A D.Fungi and Food Spoilage[M]. Aspen Publishers Inc, Gaithersburg, 1999: 593.
[18] Samson RA, Hoekstra ES, Frisvad JC, et al. Introduction to Food- and Airborne Fungi(6th edition)[M]. Utrecht: Centraalbureau voor Schimmelcultures, 2002: 389.
[19] Beuchat L R, Hwang C A.Evaluation of modified dichloran 18% glycerol (DGl8) agar for enumerating fungi in wheat flour: a collaborative study[J]. International Journal of Food Microbiology, 1996(29): 161~166.
[20] Deak T, Chen J, Golden D.A, et al. Comparison of dichloran 18% glycerol (DG18) agar with general purpose mycological media for enumerating food spoilage yeasts[J]. International Journal of Food Microbiology, 2001: 49~53.
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