Team:USTC CHINA/Modeling/B.SubtilisCulture
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<h1>Why Do We Design This Experiment</h1> | <h1>Why Do We Design This Experiment</h1> | ||
- | <p align="justify">B.subtilis has been widely applied as engineered bacteria, especially in food industry and pharmaceutical industry, for its safety and excellent secretion capacity. Therefore, after comparing characters of distinct mutants we selected B.subtilis WB800N mutant as our engineered bacteria and looked up plenty of papers to select the optimal conditions for our experiment. To our disappointment, very few experiments have been done on WB800N mutant, and most optimization experiments regarding B.subtilis focus solely on the optimization of production of specific proteins produced by B.subtilis. Consider the final goal of our project, it is imperative to design this experiment on our own to find out the best condition for B.subtilis WB800N.</p> | + | <p align="justify"><i>B.subtilis</i> has been widely applied as engineered bacteria, especially in food industry and pharmaceutical industry, for its safety and excellent secretion capacity. Therefore, after comparing characters of distinct mutants we selected <i>B.subtilis</i> WB800N mutant as our engineered bacteria and looked up plenty of papers to select the optimal conditions for our experiment. To our disappointment, very few experiments have been done on WB800N mutant, and most optimization experiments regarding <i>B.subtilis</i> focus solely on the optimization of production of specific proteins produced by <i>B.subtilis</i>. Consider the final goal of our project, it is imperative to design this experiment on our own to find out the best condition for <i>B.subtilis</i> WB800N.</p> |
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<h1>Sweeping Factors</h1> | <h1>Sweeping Factors</h1> | ||
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- | The first step of any methods of DOE is to investigate all variables that affect the results and select controllable factors for the experiment. In terms of this experiment, all factors can be categorized into two kinds: environment factors, like temperature, the rotation speed of the shaker, and the components of the medium. We have looked up several papers about the optimization experiments on B.subtilis, finding the rotation speed of shakers ranging from 100 r/min to 250 r/min, and generally rotation speed only plays a tiny role. Additionally, our lab has only two shakers. While we can place twenty different mediums into one shaker at a time, we must run the shakers every time we alert the speed, which surely consumes longer time. Thus, we fixed the rotation speed of shakers at 200r/min. However, temperature and inoculation time are both vital environment factors whose effects cannot be ignored.</br> | + | The first step of any methods of DOE is to investigate all variables that affect the results and select controllable factors for the experiment. In terms of this experiment, all factors can be categorized into two kinds: environment factors, like temperature, the rotation speed of the shaker, and the components of the medium. We have looked up several papers about the optimization experiments on <i>B.subtilis</i>, finding the rotation speed of shakers ranging from 100 r/min to 250 r/min, and generally rotation speed only plays a tiny role. Additionally, our lab has only two shakers. While we can place twenty different mediums into one shaker at a time, we must run the shakers every time we alert the speed, which surely consumes longer time. Thus, we fixed the rotation speed of shakers at 200r/min. However, temperature and inoculation time are both vital environment factors whose effects cannot be ignored.</br> |
Inoculation amount and pack amount are also two factors that affect results slightly. We fixed them at 5 percent and 30mL/500mL respectively according to earlier authentic experiments.</br> | Inoculation amount and pack amount are also two factors that affect results slightly. We fixed them at 5 percent and 30mL/500mL respectively according to earlier authentic experiments.</br> | ||
A typical medium consists of carbon source, nitrogen source and inorganic salt, all of which are essential to ensure the regular metabolism of engineered bacteria. Finally in light of convenience, we infered the components of typical LB medium and determined three independent medium factors: peptone, yeast extract and sodium chloride (NaCl). Peptone provides nitrogen and carbon for the colonies, while yeast extract contains most required inorganic salt, therefore we did not list any inorganic salt except NaCl. We had no idea why NaCl is listed alone, and we suspected the influence of NaCl as yeast extract had already contains sodium.</br> | A typical medium consists of carbon source, nitrogen source and inorganic salt, all of which are essential to ensure the regular metabolism of engineered bacteria. Finally in light of convenience, we infered the components of typical LB medium and determined three independent medium factors: peptone, yeast extract and sodium chloride (NaCl). Peptone provides nitrogen and carbon for the colonies, while yeast extract contains most required inorganic salt, therefore we did not list any inorganic salt except NaCl. We had no idea why NaCl is listed alone, and we suspected the influence of NaCl as yeast extract had already contains sodium.</br> | ||
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One remarkable character of CCD is that it is sequential, which is also the essence of RSM. Since we had got the fitting function, the next step is to calculate the gradient of the function, and define a small number as step length. Further experiments are supposed to be conducted from the beginning point according to the gradient and step length, and the final maximal treatment would be made sure. The methodology of RSM seems like climbing a mountain whose peak is unknown, and we are supposed to adjust our orientation according to the topography. The fitting surface, which can be often a super surface in higher dimensional spaces, can be likened to the mountain without clear peaks, and calculating gradient to orientating.</br> | One remarkable character of CCD is that it is sequential, which is also the essence of RSM. Since we had got the fitting function, the next step is to calculate the gradient of the function, and define a small number as step length. Further experiments are supposed to be conducted from the beginning point according to the gradient and step length, and the final maximal treatment would be made sure. The methodology of RSM seems like climbing a mountain whose peak is unknown, and we are supposed to adjust our orientation according to the topography. The fitting surface, which can be often a super surface in higher dimensional spaces, can be likened to the mountain without clear peaks, and calculating gradient to orientating.</br> | ||
- | Unfortunately our remaining time is not enough to support further experiments, and as we looked up other researches utilizing RSM, none of which did second round experiment, and we realized perhaps that was the difference between a scientific research and a real industrial procedure. Yet the analytical methodology of response surface still acted as a powerful tool for ANOVA. Roughly, we could consider the treatment of No. 15 medium (Temperature 35℃, Time 12h, Peptone 15, Yeast Extract 7.5, NaCl 15)as the maximal condition for B.subtilis. | + | Unfortunately our remaining time is not enough to support further experiments, and as we looked up other researches utilizing RSM, none of which did second round experiment, and we realized perhaps that was the difference between a scientific research and a real industrial procedure. Yet the analytical methodology of response surface still acted as a powerful tool for ANOVA. Roughly, we could consider the treatment of No. 15 medium (Temperature 35℃, Time 12h, Peptone 15, Yeast Extract 7.5, NaCl 15)as the maximal condition for <i>B.subtilis</i>. |
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Latest revision as of 12:50, 28 October 2013