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Linjun, S.

Publications and source records attributed to Linjun, S..

2 recordsLinked to original sources

Multiomics Analysis Revealed Anti-freezing Mechanism of Staphylococcus aureus in Its Anti-freezing Strain

Frozen food is currently a common food type. However, the presence of Staphylococcus aureus contamination caused serious challenge to frozen food safety. In this study, we explored the differences between sensitive strains and anti-freeze strains through multiomics analysis such as proteomics, phosphorylated proteomics, and metabolomics studies to understand the anti-freezing mechanism of S. aureus. This study compared the proteomics, phosphorylated proteomics and metabolomic differences between anti-freeze strains and sensitive strains before and after freezing. Before and after freezing, the differential protein-enriched channels changed from fructose-6-phosphate pathway, arachidonic acid metabolism pathway, atrazine degradation pathway to atrazine degradation pathway, starch and sucrose metabolism pathway, cysteine and methionine metabolism pathway, nitrogen metabolism pathway. In addition, this study inferred that pgi gene, ureA (urease subunit {gamma}), ureB (urease subunit ), ureC (urease subunit {beta}) gene, mtlD gene, fruB gene and asd gene could be crucial genes for the anti-freezing mechanism of S. aureus, which needs further investigation. Furthermore, the experimental results showed that PfkA, DeoC and Fda proteins from S. aureus were the key proteins for anti-freezing. They correspondingly involved in carbon fixation, fructose and mannose metabolism, and glycolysis/gluconeogenesis pathways in photosynthetic organisms. Finally, important metabolic pathways involved in the anti-freezing mechanism, mainly ABC transport pathway, amino acid metabolism pathway and secondary metabolite anabolic pathway.

microbiology↗

Molecular mechanism of acid stress response of A. acidoterrestris DSM 3922T under sublethal pH environment

Acid-responsive proteome expression profiles of Alicyclobacillus acidoterrestris (A. acidoterrestris) were analysed using label-free quantitative mass spectrometry to investigate its acid resistance mechanism at sublethal pH. Totally, 325 differential expression proteins were identified during acid stress at pH2.5 condition for 15 min, of which the expressions of 83 proteins were up-regulated and the other 242 proteins expressions were down-regulated. Differentially expressed proteins were mainly involved in organic nitrogen compounds metabolism, small molecule metabolism, organic acid metabolism and signal transduction. Overall, they were mapped into 97 metabolic pathways. Combination of KEGG pathway analysis and protein functional analysis suggested that the pH homeostasis system, changes in metabolic pathways, cell membrane permeability and DNA repair are the main acid resistance mechanisms of A. acidoterrestris at sublethal pH conditions. It is speculated that A. acidoterrestris may sense and transmit pH signals from the external environment through the nhaB protein which holds histidine-dependent acid resistance system, initiating a series of acid tolerance reactions. Our study demonstrated global physiological response of A. acidoterrestris to sublethal pH, which provided a better understanding of acid adaption mechanism of A. acidoterrestris.

microbiology↗