作者：Xihui; WANG; Hongling; LIU; Songsen; S...trehalosesynthasebacillussubtilisw800npsrfapromoterphodsignalpeptide
摘要：Bacillus subtilis is a non-pathogenic Gram-positive bacterium that has been widely used to produce industrially and pharmaceutically relevant proteins. Trehalose, a non reducing disaccharide used as protective agent and additive in foodstuffs and pharmaceutical products, can be prepared by trehalose synthase (TreS). The present work aims to construct a robust recombinant B. subtilis to achieve the secretory expression of TreS . In this study, the treS gene from Pseudomonas putida ATCC47054 was amplified by PCR and further cloned and expressed in B. subtilis WB800N using pHT01 as expression vector. For avoiding the use of inducer, promoter P srfA was used to replace the promoter P grac in pHT01 and verify the activity of recombinant trehalose synthase. The TreS activity assay was employed to evaluate the performance of recombinant B. subtilis W800N under different phosphate concentrations, carbon sources, carbon source concentrations, nitrogen sources and pH. The results showed that the P srfA promoter had a good regulation effect under pH 8.0 condition, and the enzyme activity reached 6 000 U/L. Using the PhoD as the secretory signal peptide, TreS was effectively secreted, and the extracellular enzyme activity reached 2 100 U/L, accounting for 35% of the total enzyme activity. By optimizing the medium and fermentation conditions, the extracellular enzyme activity reached 6 900 U/L in 5 L of fermentor, and the proportion reached 48%. The pHT01-P srfA -PhoD-treS secretory recombinant B. subtilis constructed in this study has great potential in trehalose synthase production.
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