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首页> 外文期刊>Le Lait >Application of Streptococcus thermophilus DPC1842 as an adjunct to counteract bacteriophage disruption in a predominantly lactococcal Cheddar cheese starter: use in bulk starter culture systems
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Application of Streptococcus thermophilus DPC1842 as an adjunct to counteract bacteriophage disruption in a predominantly lactococcal Cheddar cheese starter: use in bulk starter culture systems

机译:嗜热链球菌DPC1842作为辅助剂可抵消主要是乳球菌切达干酪发酵剂中的噬菌体破坏:在批量发酵剂培养系统中使用

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摘要

A significant amount of Cheddar cheese manufactured world-wide relies on bulk starter cultures instead of direct vat set (DVS) cultures. While the inclusion of S. thermophilus is sometimes used to counteract failure due to lactococcal phage in the latter system, it is considered difficult to implement in bulk starter systems and is normally avoided. This stems from the problem in controlling the ratio of S. thermophilus to lactococci during the bulk starter preparation such that suitable acidification rates can be achieved. The current study demonstrates how S. thermophilus numbers can be controlled during growth in the bulk starter medium prior to inoculation of a culture, based on three lactococcal strains and S. thermophilus DPC1842, into the cheese vat. The concentration of inorganic phosphate necessary to inhibit the growth of strain DPC1842 in a whey-based bulk starter medium was found to be 0.18 mol.L-1. Since higher levels of phosphate exist in different commercial bulk starter media used for mesophilic cultures, a number of these media can be used for propagation of this starter blend without domination of strain DPC1842 over its lactococcal counterparts. Strain DPC1842 is highly phage resistant and is particularly acid-fast in the cheese milk and reduces the pH efficiently at very low inocula. Cheddar cheese was manufactured in a commercial plant with this system and the resulting cheese had good flavour characteristics. This study demonstrates the effectiveness of the S. thermophilus DPC1842 component in rescuing the fermentation in the event of severe lactococcal phage attack.
机译:在全球范围内生产的切达干酪中,有大量依赖于大量的起子文化,而不是直接采用桶装(DVS)培养。尽管有时将嗜热链球菌包括在内以抵消后一种系统中由于乳球菌噬菌体引起的衰竭,但认为在批量发酵剂系统中难以实施并且通常避免。这源于在批量发酵剂制备过程中控制嗜热链球菌与乳球菌的比例的问题,从而可以实现合适的酸化速率。当前的研究表明,在将三种乳酸菌和嗜热链球菌DPC1842接种到干酪桶中后,如何在培养菌接种前在大量起始培养基中生长期间控制嗜热链球菌的数量。发现在基于乳清的大量发酵剂培养基中抑制菌株DPC1842生长所需的无机磷酸盐的浓度为0.18mol.L-1。由于用于中温培养的不同商业批量发酵剂培养基中存在较高水平的磷酸盐,因此许多此类培养基可用于发酵该发酵剂混合物,而菌株DPC1842在其乳球菌对应物中没有优势。 DPC1842菌株具有高度的噬菌体抗性,在干酪乳中特别耐酸,并且在极低接种量下即可有效降低pH值。切达干酪是用这种系统在商业工厂生产的,所得干酪具有良好的风味特征。这项研究证明,如果发生严重的乳球菌噬菌体攻击,嗜热链球菌DPC1842组分在挽救发酵中的有效性。

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