De Bellis Palmira, Ferrara Massimo, Bavaro Anna Rita, Linsalata Vito, Di Biase Mariaelena, Musio Biagia, Gallo Vito, Mulè Giuseppina, Valerio Francesca
Institute of Sciences of Food Production (ISPA), National Research Council (CNR), Via G. Amendola 122/O, 70126 Bari, Italy.
Department of Civil, Environmental, Land, Building and Chemical Engineering, Dicatech, Polytechnic University of Bari, Via Edoardo Orabona 4, 70125 Bari, Italy.
Foods. 2022 Sep 13;11(18):2819. doi: 10.3390/foods11182819.
A metabolic feature of lactic acid bacteria (LAB) is the production of exopolysaccharides (EPSs), which have technological and functional properties of interest to the food sector. The present study focused on the characterization of the strain C43-11, a high EPS producer in the presence of sucrose, in comparison with a low-producing strain (C2-32), and on possible genetic regulatory elements responsible for the modulation of () genes expression. NMR analysis of the polymeric material produced by the C43-11 strain indicated the presence of dextran consisting mainly of a linear scaffold formed by α-(1-6) glycosidic linkages and a smaller amounts of branches derived from α-(1-2), α-(1-3), and α-(1-4) linkages. Molecular analysis of the genes and the putative transcriptional promoters of the two strains showed differences in their regulatory regions. Such variations may have a role in the modulation of expression levels in the presence of sucrose. The strong upregulation of the gene in the C43-11 strain resulted in a high accumulation of EPS. This is the first report showing differences in the regulatory elements of the gene in and indicates a new perspective of investigation to identify the regulatory mechanism of EPS production.
乳酸菌(LAB)的一个代谢特征是产生胞外多糖(EPSs),这些胞外多糖具有食品行业感兴趣的技术和功能特性。本研究重点在于对菌株C43 - 11进行特性描述,该菌株在蔗糖存在下是高产EPS的菌株,将其与低产菌株(C2 - 32)进行比较,并研究可能负责调节()基因表达的遗传调控元件。对C43 - 11菌株产生的聚合材料进行核磁共振分析表明,存在主要由α -(1 - 6)糖苷键形成的线性支架以及少量源自α -(1 - 2)、α -(1 - 3)和α -(1 - 4)键的分支组成的右旋糖酐。对这两种菌株的基因和假定转录启动子进行分子分析显示,它们的调控区域存在差异。这种差异可能在蔗糖存在时对基因表达水平的调节中发挥作用。C43 - 11菌株中基因的强烈上调导致了EPS的大量积累。这是首次报道在中基因调控元件存在差异,并表明了一个新的研究视角,即确定EPS产生的调控机制。