Difference between revisions of "Team:NYMU-Taipei/Nitrogen starvation"

Background

　　With the development of global economy in the latest demands of energy in world, an average Taiwanese produces around 2.58 metric tons of carbon emission a year. This number far surpasses those of China, Japan and South Korea. Our project, as a result, works to use biofuel as an alternative fossil fuel to reduce the current energy crisis. In our lab, we use microalgae as the source of biofuel since they have the greatest capability of producing large amount of oil.

　　Our project aims to increase oil accumulation through nitrogen starvation, which was brought up in a research we came upon. Under nitrogen starvation, de novo synthesis of triacylglycerol from acyl-CoA increases. Acyl moieties derived from the degradation of membrane lipids then recycle into triacylglycerol, increasing carbon flux towards glycerol-3 -phosphate and acyl-CoA for fatty acid synthesis. As such, the oil accumulation under nitrogen starvation will increase.

　　There are currently two types of cultivated systems: open-pond and closed bioreactors. While open-pond costs way lower than closed bioreactors, open-pond cultivate microalgae is with significantly lower oil contents. Many microalgae farms today cultivate microalgae in closed ponds, where regulations are made to keep the nitrogen level low. This method, though, consumes lots of energy due to the need to maintain proper temperature, nutrition, light, and other growing factors. We want to develop a new method that allows microalgae to reach nitrogen starvation in open-pond, and thus reaching the same effectiveness of closed bioreactors with the affordable price of open-pond.

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Design

　　NrtA protein sticks to the periplasmic membrane through a flexible linker to capture nitrite or nitrate in the periplasm. Then delivery to the transmembrane complex that made by NrtB. In our project, we try to transform NrtA gene from cyanobacteria Synechocystis sp. PCC 6803 to E.coli, and then co-culture the engineered E.coli with microalgae. Engineered E.coli will be capable of clutching nitrite or nitrate present in the environment. They will not intake nitrate or nitrite since the gas accumulation may be lethal to cells. But the amount of cells that contain nitrite will decrease. Therefore, the microalgae will undergo nitrogen starvation and produce oil more efficiently.

　　After building up the nitrogen starvation and extracting oil from microalgae, we need to kill E.coli to prevent contamination. So we plan to use endolysin and holin for cell lysis, which is similar to the mechanism used by team PeKing (2014 iGEM Beijing). Holin can trigger the formation of holes on cell membrane. When holin successfully forms holes on cell membrane, endolysin can pass through the membrane to decompose peptidoglycan. E.coli is lysed after the cell membrane and cell wall are destroyed. To control the suicide timing, we designed an inducible promoter for holin, so that we can induce E.coli suicide at the exact time we want.

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Experiments

PCC 6803 gDNA extraction

NrtA expression

endolysin construct

holin construct

endolysin-holin construct

endolysin-holin-NrtA construct

*See our parts: click

*See our experiments protocols: click

Growth Curve Measurement

　　In order to investigate the optimal time to co-culture our modified E.coli and Chlorella vulgaris, evaluate growth of Chlorella vulgaris before Nile Red staining for oil determination in microalgal cells, we will measure the OD value at 680nm by using the spectrophotometer and analyze the growth curve in R.
　　However, we encountered some difficulties such as irregular measurement time and personal errors. Thus, we decided to search for better measurement method. Later, we borrowed a photo-bioreactor from Professor Ya Tang Yang, Department of Electrical Engineering, National Tsing Hua University, and used it to measure OD value for more precise bacterial growth curves.

　　

1. The above line chart presents growth curve of Chlorella vulgaris. This measurement lasted more than 216 hours and it roughly meets our expectation.
2. Although the later part of growth curve shows violent fluctuating range, it may be affected by environmental nitrogen metabolites from Chlorella vulgaris.
3. The measurement result helps us determine lipid production of Chlorella vulgaris, and the time we add NrtA-transformed E. coli into the medium to establish a co-culture system.

Automatic Measurement

　　In the photo-bioreactor, there are four light-emitting diode sources and two photodetectors. Once calibrated, the device can cultivate microbial cells and record their growth expression without human intervention. We measure two kinds of microalgae during cell growth in same culture medium, BG-11.

　　The photo-bioreactor was designed by Professor Yang. It was made with Arduino and some circuit components. Yang’s students also helped us assemble and teach us how to use this device. The photo-bioreactor itself can detect multiple units of organisms at same time, has pumps, fans, stir bars and some light bars. In Yang’s laboratory, we created a calibration curve for correcting and confirmed that there was a very high degree of correlation between voltage and OD value. This can be observed in the charts below.

And here are our results.

1. The above line chart presents growth curve of Chlorella vulgaris, under measurement near 10000 minutes made by the photo-bioreactor.
2. In comparison to the stimulation model we made, the result meets our expectation.

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NrtA Functional Test

PCC 6803 gDNA extraction

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Suicide Mechanism Functional Test

　　Before we construct our suicide mechanism with NrtA, we want to make sure that our suicide mechanism, endolysin and holin, can be induced by lactose efficiently. Therefore, we test our suicide mechanism by adding different concentration of lactose in order to find out the minimum effective concentration. Furthermore, to induce E.coli suicide at the time we want, we also want to know the changing degree of the OD value of bacterium at different time after the lactose is added.

　　We measure the OD₆₀₀ value of the sample, and then aliquot liquid culture into several cuvettes. Next, we add different amount of 0.5mM lactose into cuvettes to form different concentration of lactose, and measure the OD₆₀₀ value per hour.

　　As the figure shows, the suicide mechanism is induced immediately when lactose is added into the samples. Besides, we can see that the lactose concentration and the degree of decline of OD value are positively correlated.

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Reference