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首页> 外文期刊>Journal of applied microbiology >Lactococcus lactis DPC5598, a plasmid-free derivative of a commercial starter, provides a valuable alternative host for culture improvement studies
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Lactococcus lactis DPC5598, a plasmid-free derivative of a commercial starter, provides a valuable alternative host for culture improvement studies

机译:乳酸乳球菌DPC5598,一种商业发酵剂的无质粒衍生物,为培养改良研究提供了有价值的替代宿主

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Aims: To generate a plasmid-free derivative of an extensively used industrial starter strain Lactococcus lactis DPC4268, which could be used as a backbone strain for starter improvement programmes. Methods and Results: DPC4268 containing four large plasmids was subjected to high temperature plasmid curing resulting in derivatives, each with a different plasmid complement of one, two or three different plasmids in addition to a plasmid-free derivative. Industrially relevant phenotypes were assigned to each plasmid on the basis of detailed phenotypic and genetic analyses and these were (a) proteinase activity (Prt, 60 kb) (b) lactose fermentation (Lac, 55 kb) (c) bacteriophage adsorption inhibition (Ads, 44 kb) and (d) type I restriction/ modification (R/M, 40 kb). The plasmid-free variant of DPC4268 was shown to be transformable at frequencies comparable to the common laboratory strain L. lactis MG1614. Furthermore its genome was demonstrated to be significantly different from the laboratory strains L. lactis MG1614 and the recently sequenced L. lactis IL1403 genomes by pulsed-field gel electrophoresis. Conclusions: This study produced an easily transformable plasmid-free derivative which was genomically different from both MG1614 and IL1403. In addition, important plasmid-borne industrial traits, including two phage-resistance mechanisms, were identified in DPC4268. Significance and Impact of the Study: L. DPC4268 is a vitally important commercial strain used in the manufacture of Cheddar cheese. The generation of a plasmid-free derivative may provide an important backbone strain as a basis for future strain improvement purposes.
机译:目的:产生广泛使用的工业发酵菌株乳酸乳球菌DPC4268的无质粒衍生物,其可用作发酵改良计划的骨干菌株。方法和结果:将含有四个大质粒的DPC4268进行高温质粒固化,得到衍生物,除了不含质粒的衍生物外,每个衍生物还具有一个,两个或三个不同质粒的不同质粒互补序列。在详细的表型和遗传分析的基础上,将与工业相关的表型分配给每个质粒,它们是(a)蛋白酶活性(Prt,60 kb)(b)乳糖发酵(Lac,55 kb)(c)噬菌体吸附抑制(Ads (44 kb)和(d)I型限制/修饰(R / M,40 kb)。已显示DPC4268的无质粒变异体可在与普通实验室菌株乳酸乳球菌MG1614相当的频率下转化。此外,通过脉冲场凝胶电泳证明其基因组与实验室菌株乳酸乳球菌MG1614和最近测序的乳酸乳球菌IL1403基因组显着不同。结论:该研究产生了易于转化的无质粒衍生物,其在基因组上与MG1614和IL1403均不同。此外,在DPC4268中鉴定出重要的质粒携带的工业性状,包括两个噬菌体抗性机制。该研究的意义和影响:L. DPC4268是用于切达干酪生产中至关重要的商业菌株。无质粒衍生物的产生可提供重要的主链菌株,作为未来菌株改良目的的基础。

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