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1.
Electron. j. biotechnol ; 19(4): 62-67, July 2016. ilus
Article Dans Anglais | LILACS | ID: lil-793954

Résumé

Background: A thermostable lipase MAS1 from marine Streptomyces sp. strain was considered as a potential biocatalyst for industrial application, but its production level was relatively low. Here, the effect of chaperones co-expression on the secretory expression of lipase MAS1 in Pichia pastoris was investigated. Result: Co-expression of protein disulfide isomerase (PDI), HAC1 and immunoglobulin binding protein could increase the expression level of lipase MAS1, whereas co-expression of Vitreoscilla hemoglobin showed a negative effect to the lipase MAS1 production. Among them, PDI co-expression increased lipase MAS1 expression level by 1.7-fold compared to the control strain harboring only the MAS1 gene. Furthermore, optimizing production of lipase MAS1 with Pichia pastoris strain X-33/MAS1-PDI in a 30-L bioreactor were conducted. Lower induction temperature was found to have a benefit effect for lipase MAS1 production. Lipase activity at 24 and 22°C showed 1.7 and 2.1-fold to that at 30°C, respectively. Among the induction pH tested, the highest lipase activity was obtained at pH 6.0 with activity of 440 U/mL after 144 h fermentation. Conclusion: Our work showed a good example for improving the production of recombinant enzymes in Pichia pastoris via chaperon co-expression and fermentation condition optimization.


Sujets)
Streptomyces/métabolisme , Triacylglycerol lipase/biosynthèse , Pichia , Température , Survie cellulaire , Chaperons moléculaires , Bioréacteurs , Protein Disulfide-Isomerases , Vitreoscilla , Fermentation , Techniques de culture cellulaire en batch , Concentration en ions d'hydrogène
2.
Acta Pharmaceutica Sinica ; (12): 355-360, 2011.
Article Dans Chinois | WPRIM | ID: wpr-348951

Résumé

In the present study, the regulation of Vitreoscilla hemoglobin (VHb) on astragaloside IV biosynthesis was investigated. An intermediate expression vector consisting of the CaMV35S promoter fused to the vgb and nopaline synthase terminator was transferred into Astragalus membranaceus via Agrobacterium rhizogenes. The transgenic hairy roots were confirmed by PCR amplification and Southern blot hybridization. The expression of vgb in transgenic hairy roots was confirmed by RT-PCR. After 15 days cultivation, the dry weight and growth rate of transgenic hairy roots were higher than that of the non-transgenic hairy root. ELSD-HPLC analysis showed that astragaloside IV content of transgenic hairy roots was 5 to 6 times of non-transgenic hairy root control and 10 to 12 times of Radix Astragali from Shanxi Province. These results suggested that the expression of vgb promoted the growth of transgenic hairy roots, and increased the content of astragaloside IV.


Sujets)
Astragalus membranaceus , Génétique , Métabolisme , Protéines bactériennes , Génétique , Métabolisme , Racines de plante , Métabolisme , Végétaux génétiquement modifiés , Génétique , Métabolisme , Plantes médicinales , Génétique , Métabolisme , Saponines , Triterpènes , Hémoglobines tronquées , Génétique , Métabolisme , Vitreoscilla , Génétique
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