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首页> 外文期刊>Journal of Microbiological Methods >Evaluation of a quantitative screening method for hydrogen sulfide production by cheese-ripening microorganisms: the first step towards l-cysteine catabolism
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Evaluation of a quantitative screening method for hydrogen sulfide production by cheese-ripening microorganisms: the first step towards l-cysteine catabolism

机译:干酪成熟微生物生产硫化氢的定量筛选方法的评估:迈向l-半胱氨酸分解代谢的第一步

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A practical adaptation of the methylene blue reaction for hydrogen sulfide quantification was developed to perform microbial selection. Closed plate flasks containing a zinc-agar layer above the liquid microbial culture are proposed as a trap system where the H(2)S can be retained and then quantified by the methylene blue reaction. Using this quantitative method, the ability to produce H(2)S was studied in several cheese-ripening microorganisms. Our aim was to select strains that produce the highest quantities of H(2)S as the main product of L-cysteine catabolism. Thirty seven yeast and bacteria strains were cultivated with or without L-cysteine. The separation between the growth medium and the H(2)S trapping layer displayed good performance: all the studied strains grew efficiently and only negligible loss of H(2)S was observed during culturing. The strains displayed large differences in their H(2)S production capabilities: yeast strains were greater producers of H(2)S than bacteria with production strain-related in both cases. Furthermore, the relationship between H(2)S production and L-cysteine consumption was analyzed, which made it possible for us to select microorganisms with high capacity in L-cysteine degradation. The production of volatile sulfur compounds was also studied and the possible effect of culture pH and metabolic differences between strains are discussed.
机译:开发了一种实用的亚甲基蓝反应用于硫化氢定量的方法,可以进行微生物选择。建议在液体微生物培养物上方包含锌-琼脂层的封闭平板烧瓶中,作为捕集系统,在其中可以保留H(2)S,然后通过亚甲基蓝反应进行定量。使用这种定量方法,研究了几种奶酪成熟微生物中产生H(2)S的能力。我们的目的是选择产生最高量的H(2)S作为L-半胱氨酸分解代谢的主要产物的菌株。在有或没有L-半胱氨酸的情况下培养了37个酵母和细菌菌株。生长培养基和H(2)S捕集层之间的分离显示出良好的性能:所有研究的菌株高效生长,并且在培养过程中仅观察到可忽略的H(2)S损失。这些菌株在H(2)S生产能力上显示出很大的差异:在这两种情况下,酵母菌株比与生产菌株相关的细菌是H(2)S的更大生产者。此外,分析了H(2)S产量与L-半胱氨酸消耗量之间的关系,这使我们有可能选择具有高降解L-半胱氨酸能力的微生物。还研究了挥发性硫化合物的产生,并讨论了培养液pH值和菌株之间代谢差异的可能影响。

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