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Tryptophan catabolism in Brevibacterium linens BL2.

机译:短杆菌属BL2中的色氨酸分解代谢。

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摘要

Recent studies suggest aromatic amino acid catabolism by starter lactococci and flavor adjunct bacteria have a significant impact on off-flavor development during Cheddar cheese ripening. We hypothesized that a flavor adjunct bacterium, Brevibacterium linens BL2, produces off-flavor compounds from aromatic amino acid metabolism that will have a detrimental impact on cheese flavor.; The mechanism of tryptophan (Trp) catabolism in Brevibacterium linens BL2, was investigated in a chemically defined medium during incubation in laboratory conditions (no carbohydrate, pH 6.50, 220 rpm, 25°C) and cheese-like conditions (no carbohydrate, 4% NaCl, static incubation, 15°C). In laboratory conditions, metabolic studies and enzyme assays confirmed that Trp was converted to kynurenine and anthranilic acid. However, cells incubated in cheese-like conditions did not utilize Trp, indicating that these enzymes are not likely to be involved in formation of Trp compounds associated with off-flavors in Cheddar cheese.; In an attempt to verify the metabolic activity of the cells during incubation by monitoring the amino acid metabolism in chemically defined medium inoculated with B. linens BL2, a capillary electrophoresis-laser-induced fluorescence method was developed that could separate, detect, and quantitate 18 amino acids within 38 min. The data indicated that B. linens BL2 was metabolically active. Presumably, the cells will be metabolically active and metabolize amino acids in cheese as well.; The ability to determine the Trp metabolic activity of B. linens BL2 in cheese, and to quantify Trp catabolic compounds in cheese during ripening, requires a quantitative extraction procedure. An analytical method was developed to extract and quantify aromatic amino acids and Trp catabolites from cheese using capillary electrophoresis. Methanol was used to extract Cheddar cheese made with Lactococcus lactis S3 alone and in combination with B. linens BL2 to quantitatively determine the influence of BL2 on the occurrence of aromatic catabolites. All cheeses contained aromatic amino acids, indole acetic acid, and indole. The concentration and time taken for development of these compounds were significantly decreased or delayed by the addition of B. linens BL2. After 6 months of aging, the concentrations of Trp catabolites were significantly lower in cheese made with B. linens BL2. Addition of BL2 did not directly contribute to off-flavors derived from Trp catabolism in Cheddar cheese. Therefore, the hypothesis was rejected.
机译:最近的研究表明,起始乳球菌和风味辅助细菌对芳香族氨基酸的分解代谢对切达干酪成熟期间异味的产生有重大影响。我们假设,风味辅助细菌短杆菌属 BL2,会从芳香族氨基酸代谢中产生异味化合物,这将对奶酪的风味产生不利影响。在实验室条件下(无碳水化合物,pH 6.50、220 rpm,25°C)和类似干酪的条件下孵育期间,在化学成分确定的培养基中研究了短杆菌属 BL2中色氨酸(Trp)分解代谢的机理。条件(无碳水化合物,4%NaCl,静态孵育,15°C)。在实验室条件下,代谢研究和酶分析证实Trp转化为犬尿氨酸和邻氨基苯甲酸。然而,在类似干酪的条件下培养的细胞没有利用Trp,这表明这些酶不太可能参与与切达干酪中异味相关的Trp化合物的形成。为了通过在接种了 B的化学成分确定的培养基中监测氨基酸代谢,来验证培养过程中细胞的代谢活性。亚麻BL2是一种毛细管电泳-激光诱导的荧光方法,可以在38分钟内分离,检测和定量18种氨基酸。数据表明<斜体> B。亚麻BL2具有代谢活性。据推测,这些细胞将具有代谢活性,并且也会代谢奶酪中的氨基酸。确定 B的Trp代谢活性的能力。奶酪中的亚麻 BL2,以及在成熟过程中定量奶酪中的Trp分解代谢化合物,需要定量提取程序。开发了一种使用毛细管电泳从奶酪中提取和定量芳香族氨基酸和Trp分解代谢物的分析方法。甲醇被用来提取切达干酪,该切达干酪仅由乳酸乳球菌 S3制成,并与 B结合使用。亚麻BL2来定量确定BL2对芳香族分解代谢产物的影响。所有奶酪均包含芳香族氨基酸,吲哚乙酸和吲哚。添加 B显着降低或延迟了开发这些化合物的浓度和时间。亚麻 BL2。老化6个月后,用 B制成的奶酪中Trp分解代谢物的浓度明显降低。亚麻 BL2。在切达干酪中,添加BL2不会直接导致源自Trp分解代谢的异味。因此,该假设被拒绝了。

著录项

  • 作者

    Ummadi, Madhavi Soni.;

  • 作者单位

    Utah State University.;

  • 授予单位 Utah State University.;
  • 学科 Agriculture Food Science and Technology.
  • 学位 Ph.D.
  • 年度 2002
  • 页码 163 p.
  • 总页数 163
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 农产品收获、加工及贮藏;
  • 关键词

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