Development of Rapid Identification and Risk Analysis of Moniliella Spp. in Acidic Processed Foods

被引:0
作者
Nakayama, Motokazu [1 ]
Hosoya, Kouichi [1 ]
Shimizu-Imanishi, Yumi [2 ]
Chibana, Hiroji [3 ]
Yaguchi, Takashi [3 ]
机构
[1] Kao Corp, Global R&D Safety Sci, 2606 Akabane, Ichikai, Tochigi 3213497, Japan
[2] Kanto Gakuin Univ, Coll Engn, Dept Appl Mat & Life Sci, Kanazawa Ku, 1-50-1 Mutsuura Higashi, Yokohama, Kanagawa 2368501, Japan
[3] Chiba Univ, Med Mycol Res Ctr, Chuo Ku, 1-8-1 Inohana, Chiba 2608673, Japan
关键词
Acetic acid resistance; Adaptation; Ethanol resistance; Moniliella; Rapid identification; SP NOV; YEASTS;
D O I
暂无
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The number of spoilage incidents in the food industry attributable to a species of the genus Moniliella has recently increased, but the risk of food spoilage has not yet been evaluated. The purpose of this study was to develop a method to rapidly identify high-risk species and to conduct a risk analysis study of Moniliella spp. Acetic acid resistance of M. acetoabutens and ethanol resistance of M. suaveolens were higher than for other Moniliella species. All examined strains of M. acetoabutens developed a high tolerance to acetic acid by being cultured twice in liquid media containing low concentrations of acetic acid. These findings indicate that M. acetoabutens and M. suaveolens are high-risk species for food spoilage and must be discriminated from other fungi. We developed species-specific primers to identify M. acetoabutens and M. suaveolens using the polymerase chain reaction (PCR) to amplify the D1/D2 domain of 28S rDNA. The PCR using the primer sets designed for M. acetoabutens (Mac_F1/R1) and M. suaveolens (Msu_F1/R1) was specific to the target species and did not detect other fungi involved in food spoilage or environmental contamination. This method is expected to be effective for the monitoring of raw materials and components of the food production process.
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页码:73 / 80
页数:8
相关论文
共 18 条
  • [1] Aou T., 1992, J ANTIBACT ANTIFUNG, V20, P381
  • [2] Food spoilage yeasts: effects of pH, NaCl and temperature on growth
    Betts, GD
    Linton, P
    Betteridge, RJ
    [J]. FOOD CONTROL, 1999, 10 (01) : 27 - 33
  • [3] Dakin J. C., 1968, Journal of Food Technology, V3, P49
  • [4] De Hoog G S., 1979, Studies in Mycology, V19, P1
  • [5] Entani E., 2000, J BREW SOC JPN, V95, P39
  • [6] Hitokoto H., 1987, JAPANESE J FOOD MICR, V4, P149
  • [7] Risk analysis and rapid detection of the genus Thermoascus, food spoilage fungi
    Hosoya, Kouichi
    Nakayama, Motokazu
    Tomiyama, Daisuke
    Matsuzawa, Tetsuhiro
    Imanishi, Yumi
    Ueda, Seiichi
    Yaguchi, Takashi
    [J]. FOOD CONTROL, 2014, 41 : 7 - 12
  • [8] Risk analysis and development of a rapid method for identifying four species of Byssochlamys
    Hosoya, Kouichi
    Nakayama, Motokazu
    Matsuzawa, Tetsuhiro
    Imanishi, Yumi
    Hitomi, Jun
    Yaguchi, Takashi
    [J]. FOOD CONTROL, 2012, 26 (01) : 169 - 173
  • [9] Identification of clinically important ascomycetous yeasts based on nucleotide divergence in the 5' end of the large-subunit (26S) ribosomal DNA gene
    Kurtzman, CP
    Robnett, CJ
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (05) : 1216 - 1223
  • [10] Morozumi S., 1988, FOOD CHEM, V5, P30