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嗜热链球菌半乳糖激酶阳性重组菌株的特性分析

Characterization of a galactokinase-positive recombinant strain of Streptococcus thermophilus.

作者信息

Vaillancourt Katy, LeMay Jean-Dominique, Lamoureux Maryse, Frenette Michel, Moineau Sylvain, Vadeboncoeur Christian

机构信息

Groupe de Recherche en Ecologie Buccale, Département de Biochimie et de Microbiologie, Faculté des Sciences et de Génie, and Faculté de Médecine Dentaire, Université Laval, Quebec City, Quebec, Canada G1K 7P4.

出版信息

Appl Environ Microbiol. 2004 Aug;70(8):4596-603. doi: 10.1128/AEM.70.8.4596-4603.2004.

Abstract

The lactic acid bacterium Streptococcus thermophilus is widely used by the dairy industry for its ability to transform lactose, the primary sugar found in milk, into lactic acid. Unlike the phylogenetically related species Streptococcus salivarius, S. thermophilus is unable to metabolize and grow on galactose and thus releases substantial amounts of this hexose into the external medium during growth on lactose. This metabolic property may result from the inability of S. thermophilus to synthesize galactokinase, an enzyme of the Leloir pathway that phosphorylates intracellular galactose to generate galactose-1-phosphate. In this work, we report the complementation of Gal(-) strain S. thermophilus SMQ-301 with S. salivarius galK, the gene that codes for galactokinase, and the characterization of recombinant strain SMQ-301K01. The recombinant strain, which was obtained by transformation of strain SMQ-301 with pTRKL2TK, a plasmid bearing S. salivarius galK, grew on galactose with a generation time of 55 min, which was almost double the generation time on lactose. Data confirmed that (i) the ability of SMQ-301K01 to grow on galactose resulted from the expression of S. salivarius galK and (ii) transcription of the plasmid-borne galK gene did not require GalR, a transcriptional regulator of the gal and lac operons, and did not interfere with the transcription of these operons. Unexpectedly, recombinant strain SMQ-301K01 still expelled galactose during growth on lactose, but only when the amount of the disaccharide in the medium exceeded 0.05%. Thus, unlike S. salivarius, the ability to metabolize galactose was not sufficient for S. thermophilus to simultaneously metabolize the glucose and galactose moieties of lactose. Nevertheless, during growth in milk and under time-temperature conditions that simulated those used to produce mozzarella cheese, the recombinant Gal(+) strain grew and produced acid more rapidly than the Gal(-) wild-type strain.

摘要

嗜热链球菌这种乳酸菌因其能将乳糖(牛奶中的主要糖类)转化为乳酸的能力而被乳制品行业广泛使用。与系统发育相关的唾液链球菌不同,嗜热链球菌无法代谢半乳糖并在其上生长,因此在以乳糖为生长底物时会将大量这种己糖释放到外部培养基中。这种代谢特性可能是由于嗜热链球菌无法合成半乳糖激酶,半乳糖激酶是Leloir途径中的一种酶,可将细胞内半乳糖磷酸化以生成半乳糖 -1- 磷酸。在这项工作中,我们报道了用编码半乳糖激酶的唾液链球菌galK对Gal(-)菌株嗜热链球菌SMQ - 301进行互补,并对重组菌株SMQ - 301K01进行了表征。重组菌株是通过用携带唾液链球菌galK的质粒pTRKL2TK转化菌株SMQ - 301获得的,它在半乳糖上生长,代时为55分钟,几乎是在乳糖上生长代时的两倍。数据证实:(i) SMQ - 301K01在半乳糖上生长的能力源于唾液链球菌galK的表达;(ii) 质粒携带的galK基因的转录不需要GalR(gal和lac操纵子的转录调节因子),并且不干扰这些操纵子的转录。出乎意料的是,重组菌株SMQ - 301K01在以乳糖为生长底物时仍会排出半乳糖,但仅当培养基中双糖的量超过0.05%时才会如此。因此,与唾液链球菌不同,对于嗜热链球菌来说,代谢半乳糖的能力不足以使其同时代谢乳糖的葡萄糖和半乳糖部分。然而,在牛奶中生长以及在模拟用于生产马苏里拉奶酪的时间 -温度条件下,重组Gal(+)菌株比Gal(-)野生型菌株生长得更快且产酸更多。

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