scholarly journals Optimization of expression conditions for a novel NZ2114-derived antimicrobial peptide-MP1102 under the control of the GAP promoter in Pichia pastoris X-33

2015 ◽  
Vol 15 (1) ◽  
Author(s):  
Ruoyu Mao ◽  
Da Teng ◽  
Xiumin Wang ◽  
Yong Zhang ◽  
Jian Jiao ◽  
...  
2018 ◽  
Vol 2 (1) ◽  
pp. 23-29 ◽  
Author(s):  
Zeqiang Liu ◽  
Mingxing Zhu ◽  
Xiangjun Chen ◽  
Guimao Yang ◽  
Tiantian Yang ◽  
...  

2014 ◽  
Vol 13 (1) ◽  
pp. 57 ◽  
Author(s):  
Anikó Várnai ◽  
Campbell Tang ◽  
Oskar Bengtsson ◽  
Andrew Atterton ◽  
Geir Mathiesen ◽  
...  
Keyword(s):  

Author(s):  
Min Liu ◽  
Gabriel Potvin ◽  
Yiru Gan ◽  
Zhanbin Huang ◽  
Zisheng Zhang

Based on statistical designs, minimal salts medium, commonly used for yeast cultivation, was optimized to maximize GAP promoter-mediated phytase production by recombinant Pichia pastoris grown on glycerol. A Plackett-Burman design was followed to screen medium components to determine those that significantly affected phytase production. Of the 8 components studied, the concentrations of K2SO4, CaSO4•2H2O and MgSO4•7H2O were identified as having a significant effect. These three components were subsequently optimized by response surface methodology using a central composite design. The optimal concentrations of the three components, leading to a maximal extracellular phytase activity of 161.64 U/ml, were K2SO4 13.25g/l, CaSO4•2H2O 1.03g/l and MgSO4•7H2O 17.94g/l. The activity measured in cultures using optimized growth medium is significantly higher than the 73.31 U/ml measured in cultures using standard minimal salts media. The theoretical phytase yields predicted by the developed model were very close to experimentally obtained values.


2008 ◽  
Vol 36 (6) ◽  
pp. 1611-1619 ◽  
Author(s):  
Ai-Lian Zhang ◽  
Jin-Xian Luo ◽  
Tian-Yuan Zhang ◽  
Ying-Wen Pan ◽  
Yan-Hua Tan ◽  
...  

2008 ◽  
Vol 43 (10) ◽  
pp. 1124-1131 ◽  
Author(s):  
Lei Wang ◽  
Chun-e Lai ◽  
Qifeng Wu ◽  
Junliang Liu ◽  
Maojun Zhou ◽  
...  

2005 ◽  
Vol 49 (7) ◽  
pp. 3004-3008 ◽  
Author(s):  
Jorge Gutiérrez ◽  
Raquel Criado ◽  
María Martín ◽  
Carmen Herranz ◽  
Luis M. Cintas ◽  
...  

ABSTRACT The gene encoding mature enterocin P (EntP), an antimicrobial peptide from Enterococcus faecium P13, was cloned into the pPICZαA expression vector to generate plasmid pJC31. This plasmid was integrated into the genome of P. pastoris X-33, and EntP was heterologously secreted from the recombinant P. pastoris X-33t1 derivative at a higher production and antagonistic activity than from E. faecium P13.


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