Difference between revisions of "Team:TJU/Design"

1 Lactate producing system

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Generally material flow, information flow, together with energy flow are key factors to regulate relations among bacterial consortium. Material flow, in particular, known as the most reliable and convenient method, is adopted in our construction. Typically the substances of the flow are often necessary nutrition for bacterial survival such as essential amino acid and carbon sources.

Shewanella oneidensis can generate electricity with a relatively narrow range of carbon substrates, including lactate, acetate, formate, pyruvate and some amino acid.[1] It has been shown that Shewanella oneidensis MR-1 prefers the utilization of lactate as an energy-favorable carbon substrate as lactate-based biomass yield was higher than that for either acetate or pyruvate. Similarly, the lactate-based growth rate was much higher as well.[2] Thus, lactate is the most suitable carbon source and also the key mediator for the material flow in our system.

In order to develop a proper mechanism for lactate supply, we use Escherichia coli, a well characterized bacterium, to produce lactate. Previously, researchers has developed a system that was able to produce 142.2 g/l of L-lactate with no more than 1.2 g/l of by-products accumulated by knocking out ldhA and lldD and inserting L-LDH.[3] Consequently, E.coli has many advantages as a host for production of lactic acid, including the ability to produce optically pure lactate, rapid growth under both aerobic and anaerobic conditions, and its simple nutritional requirements.[4]

Escherichia coli grows fermentatively in glucose-containing medium under anaerobic condition with formation of a mixture of organic acids (lactate, acetate, formate and succinate) and ethanol, and lactate only takes no more than 50% of the total metabolites.[4] Since we need to provide enough material support for the growth and metabolism of Shewanella under anaerobic condition, we decide to enhance the yield of lactate by genetic engineering through two strategies:

1.1 ldh- Lactate dehydrogenase(LDH)

LDH is an enzyme found in nearly all living cells (animals, plants, and prokaryotes), which catalyzes the conversion of pyruvate to lactate with NADH serving as the coenzyme. In our project, we intend to introduce high-yield exogenous L-(+)-lactate dehydrogenase gene (ldhA) from Lactobacillus, which can produce a relatively larger amount of L-lactate for Shewanella. Naturally, E.coli can produce D-lactate by itself and the amount and the activity of lactate dehydrogenase becomes the bottleneck. We found that those two factors of enzyme are hard to change dramatically in vivo, hence we introduce exogenous ldhA into the system to convert the redundant pyruvate and subsequently provide even more sustenance for Shewanella. Similar metabolic pathway has been found in a variety of organisms, to distinguish the differences, we renamed the heterogenous L-lactate dehydrogenase gene ldhE while homogenous one keeps original ldhA.

（ldhe表征的描述和结果）

1.2 pflB knockout

PFL is a crucial enzyme in the glucose metabolism under anaerobic condition, which can catalyze one molecule of pyruvate to one molecule of formicate and one molecule of acetylcoenzyme A (AcCoA). According to metabolic pathway, pyruvate is consumed both in the PFL and LDH reactions. In the wild type E. coli, LDH reaction is not as competitive as the reaction through PFL, and therefore, knockout of the PFL related genes will contribute to redistribute the metabolic flux. When the PFL pathway is blocked, E. coli will conceivably alter the distribution of these products to overcome the imbalanced reducing equivalents caused by the pathway knockout. Therefore, knockout of pflB not only decreased the carbon flow to acetyl-CoA under anaerobic condition but also reduced the anaerobic consumption of NADH through reductive TCA. [5]

For genes knockout, we adopted a effective, easy-to-use two-step system in which the cell is first transformed with a helper plasmid harboring genes encoding the λ-Red enzymes, I-SceI endonuclease, and RecA. λ-Red enzymes expressed from the helper plasmid are used to recombineer a small ‘landing pad’, a tetracycline resistance gene (tetA) flanked by I-SceI recognition sites and landing pad regions, into the desired location in the chromosome. After tetracycline selection for successful landing pad integrants, the cell is transformed with a donor plasmid carrying the desired insertion fragment; this fragment is excised by I-SceI and incorporated into the landing pad via recombination at the landing pad regions.[6]

First round of recombineering consists of three rounds of PCR for the construction of recombinant genome cassettes which subsequently positively selected by selection markers such as Tetr. In the second step, TetA marker was released by simultaneous induction of I-SceI and Red recombinase expression which serves as a negative selection.[7] (More details in Method.)

References

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[1] Tang Y J, Meadows A L, Keasling J D. A kinetic model describing Shewanella oneidensis MR-1 growth, substrate consumption, and product secretion.[J]. Biotechnology & Bioengineering, 2007, 96(1):125–133.
[2] Feng X, Xu Y, Chen Y, et al. Integrating Flux Balance Analysis into Kinetic Models to Decipher the Dynamic Metabolism of Shewanella oneidensis MR-1[J]. Plos Computational Biology, 2011, 8(2):e1002376-e1002376.
[3] Highly efficient L-lactate production using engineered Escherichia coli with dissimilar temperature optima for L-lactate formation and cell growth.
[4] Liu H, Kang J, Qi Q, et al. Production of lactate in Escherichia coli by redox regulation genetically and physiologically.[J]. Appl Biochem Biotechnol, 2011, 164(2):162-169.
[5] Zhu J, Shimizu K, Zhu J, et al. Effect of a single-gene knockout on the metabolic regulation in Escherichia coli for D-lactate production under microaerobic condition[J]. Metabolic Engineering, 2005, 7(2):104–115.
[6] Thomas E, Kuhlman, Edward C, Cox. Site-specific chromosomal integration of large synthetic constructs.[J]. Nucleic Acids Research, 2010, 38(38).
[7] Lin Z, Xu Z, Li Y, et al. Metabolic engineering of Escherichia coli for the production of riboflavin[J]. Microbial Cell Factories, 2014, 13(1):1-12.

2 Flavins producing system

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Shewanella oneidensis MR-1, a facultative anaerobe, has been widely used as a model anode biocatalyst in microbial fuel cells (MFCs) due to its easiness of cultivation, adaptability to aerobic and anaerobic environment and both respiratory and electron transfer versatility. [1]

Particularly, EET pathway can be subdivided into direct EET and mediated EET and the latter one limits the efficiency of electron transfer between bacteria and electrode due to the deficiency of electron mediator. To regulate relations of energy and information in the consortium, flavins hold the key to success.

It is widely accepted that interfacial EET is the rate-limiting step in the EET processes which can be relieved by some redox active molecules such as quinines and metal-centered porphyrin-ring derivatives. However, those redox active molecules are generally costly and toxic to anodic electricigens. Besides, Shewanella is capable of utilizing self-secreted flavins like riboflavin (RF) to accelerate EET, which is much more efficiently than other exogenous active molecules. More specifically, riboflavin (RF) and flavin mononucleotide (FMN) enhance EET more than five times, with much lower concentrations than those needed for anthraquinone-2,6-disulfonate (AQDS) shuttling. So we choose flavins as one entry point to enhance the electricity output of MFCs. [2]

In EET model, outward current flows from interior of cells to outer membrane (OM) and extracellular anodes through a metal-reducing conduit (Mtr pathway), where electrons (from NADH, the intracellular electron carrier) flow through the menaquinol pool, CymA (inner membrane [IM] tetraheme c-type cytochromes [c-Cyts]), MtrA (periplasmic decaheme c-Cyts), MtrB (β-barrel trans-OM protein) and finally to MtrC and OmcA (two OM decaheme c-Cyts). However, the principle of how flavins function still remains controversial. [3]

Traditional model demonstrates that flavins carry the electrons from OM c-Cyts to electrode by diffusion, which has been in debate due to thermodynamic disproof. Recently, another interfacial EET model was proposed, where flavin may serve as a cofactor binding to OmcA or MtrC to dictate EET. Fully oxidized flavin (Ox) accepts one electron from reduced heme of OM c-Cyts, and binds to OM c-Cyts as a cofactor in the semiquinone (Sq) form with shifted potential. Ox/Sq redox cycling in OM c-Cyts donates electrons to electrodes in a one electron reaction mode via direct contact.[3] So by maximizing the amount of riboflavin and FMN, we may achieve a relatively high power generation and this inspired us to construct a high-yield module in the engineered bacteria.

Although Shewanella uses endogenous flavins to mediate electrons, the amount of its production is deficient and multi-tasks brought by self-engineering may also reduce the transfer efficiency. As a consequence, we introduce a series of genes for flavin production into E.coli.

The metabolic flux (figure 2) reveals the relevant pathways of riboflavin production and engineering strategies for riboflavin production. We adopted a strain with pgi, edd and eda deletion as well as a high-yield gene construction (ribABDEC with a weak RBS in ribC pathway) from previous research. (Tao, et al) Consequently, the result shows an accumulation for riboflavin(229.1mg/L), yet a relatively small amount for FMN.

However, based on co-factor model, EET pathway points out that FMN plays a critical role in electron transfer as the same as riboflavin by combining with the OmcA protein which is an essential and indispensible part for power generation. Based on this viewpoint, we also construct ribA, ribB, ribD, ribE, and ribC into our engineered bacteria and more importantly, design a strong RBS sequence upstream of the ribC. The strong RBS before ribC sequence can lead to the FMN accumulation while riboflavin consumes a bit, which may in turn, result in increase both for riboflavin and FMN as a whole. Ultimately, our result shows a impressive amount of flavins that reaches xxx and power generation arrives at xxx.

（核黄素表征描述和结果）

References

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[1] Wang X, Tao L, Wang H, et al. Improving mediated electron transport in anodic bioelectrocatalysis[J]. Chemical Communications, 2015.
[2] Okamoto A, Nakamura R, Nealson K H, et al. Bound Flavin Model Suggests Similar Electron‐Transfer Mechanisms in Shewanella and Geobacter[J]. Chemelectrochem, 2014, 1(11):1808-1812.
[3] Yang Y, Ding Y, Hu Y, et al. Enhancing Bidirectional Electron Transfer of Shewanella oneidensis by a Synthetic Flavin Pathway[J]. Acs Synthetic Biology, 2015.
[4] Lin Z, Xu Z, Li Y, et al. Metabolic engineering of Escherichia coli for the production of riboflavin[J]. Microbial Cell Factories, 2014, 13(1):1-12.

3 Co-culture MFC

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Microorganisms rarely live in isolated niches. One reason is that the maintenance of viability of these microbes may need supplementary metabolites or other signaling chemicals provided by other microbes in the ecosystems and communities.[1] Conforming to the trend of revolution, we apply the bacterial consortium in our MFC for greater power generation and increased duration.

Apart from the universal trend of nature, the mixed culture shares some unique advantages particularly in our MFC. For example, Shewanella originally can merely use few simple carbon substrates like lactate, acetate, formate, pyruvate and some amino acid.[2] However, our consortium as a whole can expand the absorption range of carbon resources and develop a more complex diagram of carbon input for Shewanella. Also, our intention is able to achieve comprehensive functions through “Labor Division” that monoculture can hardly manage. For instance, if we use only Shewanella to supply electricity, the production of flavins as well as other related reaction will inhibit current creation. These are fundamental reasons that we adopt the “mix” strategy in our project.

3.1 First Trial

Our experiment started with monoculture of Shewanella, in which we have found several important conclusions that might be used in the later trials:
(i) Shewanella alone cannot take good use of glucose as the mere carbon source to generate power.
(ii) Voltage has been improved when we add flavins to the monoculture medium, which proved that flavins indeed would help the power enhance.
(iii) As an attempt to choose a proper substance being used in the experiment, we put sodium lactate into service and found that Shewanella could achieve power output.

3.2 Second Trial:

Since we’ve constructed the lactate producing strain (ldhE), the flavin producing strain (EC10) and an engineered strain bearing both ldhE and EC10, we initiated our co-culture experiment with different labor division.

From the figure above, we found that the co-culture system with three different strains has a higher electricity output than two-strain system before 20h, showing that a more complete labor division may have a better effect in the co-culture system. It is because that we can more accurately control the amount and ratio of lactate and flavins when they are produced in separated strains.

(2 ph试纸图)

However, the electricity output dropped promptly after 30h. (as shown in figure 1). In the meanwhile, we took samples from anode finding that pH in anode was excessively low (lower than 6.2) which might not meet the survival requirement of Shewanella.

The reason of the acidity, based on our analysis, could be the overmuch glucose or the high ratio of fermentation bacteria in the system. Particularly, our medium consist of 10 g/L glucose as well as 5% LB and 95% M9 medium. Both of the possibilities above can lead to the overproduction of lactate and other acid metabolites like formic acid which are hard to consume.

So, in order to solve the pH problem, we have two strategies. Firstly, we can optimize the medium component by reducing ratio of C and N. Secondly, we would optimize the proportion of the fermentation bacteria.

Apart from that, we also found that excessive portion of zymophyte would inhibit biofilm formation of Shewanella by zymophyte taking up the spaces in electrode.

3.3 Third trial

When we have preliminarily optimized the bacterial proportion and medium compositions, we got a significant improvement of the electricity output in spite of the relatively short sustaining time.(shown as follows)

We also attempted to put the fermentation bacteria into the system some time after Shewanella. However, the later joining of fermentation bacteria will the stability of the system so that the output oscillated for a period of time. We can see from the figure**, even though the lasting time was longer than before, the maximum electricity output was still limited.

Subsequently, we arranged variable mixture for three-strain system to determine the best proportion for electricity generation. Besides, we continued to optimize the culture condition (95%M9, 5%LB and glucose 2g/L), we can see from the figure that the three-strain system had a maximum output at around 350mV and had a significant advantage over the two-strain system. Additionally, the lasting time was over 80h without any supplementary glucose, which indicated the high utilization rate of carbon source and the relatively stable relationship among the three strains.

3.4 Fourth trial

We innovatively introduced a third species, Bacillus subtilis, into our system. Considering Bacillus subtilis take KNO3 as the substrates instead of glucose in anaerobic condition, we could reduce the competition for carbon sources between two kinds of fermentation bacteria. Also it has been reported that engineered B.subtilis could get a high output of flavins which is exactly what we want. So, we choosed Bacillus subtilis as another kind of fermentation bacteria.

It can been seen from the figure**, the electricity output of three-strain co-culture system with B.subtilis could reach more than 500mV enduring around 80h, showing a great difference from the Shewanella single-strain system. Compared with two-strain system below, the three-strain system with B.subtilis also showed a visible advantage.

Future Work:

Although we made several innovative research in our project, there are still many other aspects to develop and optimize in the future.
1. We plan to find out biofilm parts of E.coli and modify several key point to reduce adhesion effect.
2. We need to further adjust ratio of our three-strain system to bring a quicker speed toward maximum.
3. Keeping power generation unchanged, we can reduce the volume of our device so that it will increase current density.
4. Making improvements in Shewanella for more electricity output. We intend to weaken any other unrelated functions except for power production in Shewanella and using co-culture system to produce necessary nutrition for its survival.

References

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[1] Song H, Ding M Z, Jia X Q, et al. Synthetic microbial consortia: from systematic analysis to construction and applications[J]. Chem.soc.rev, 2014, 43(20):6954-6981.
[2] Tang Y J, Meadows A L, Keasling J D. A kinetic model describing Shewanella oneidensis MR-1 growth, substrate consumption, and product secretion.[J]. Biotechnology & Bioengineering, 2007, 96(1):125–133.

4 Proteolysis system

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During the experiment, our MFC in anaerobic condition has been found to reach an unexpected lower pH that showed harmful to bacterial consortium. On account of improving the rate of survival, we designed a “Sensing- Regulating” system to consume the accumulated lactate and keep the environment at a proper acid level. Our system belongs to proteomic regulation, which contains pH sensing system and orthogonal proteolysis system for self-regulating. The delayed effect within our sensing system brings us a more precise depict of possible result that the pH may oscillate at a certain range.

4.1 Sensing

Every genus of cell has an optimum range of pH to live and Shewanella along with E.coli is no exception. Previous research has identified that Shewanella can maintain a maximal population density when pH keeps above 6.2 while E.coli can survive in 5.6~8.1.[1] As an attempt to develop the superior sensing mechanism, we screen out promoter 170 (P170) and regulatory protein RcfB and introduce them into E.coli for adaption.

P170, a strongly acid-inducible promoter from Lactococcus lactis, is up-regulated at low pH during the transition to stationary phase.[2] The trans-acting protein RcfB, however, is involved in basal activity of P170 and is also essential for pH induction. The protein RcfB, upon activation by lactate, bind a DNA recognition motif within a promoter region and activates transcription.[3] When the cells are exposed to acid environments, the RcfB activation by an ‘acid’ signal allows its binding to the ACiD-box, resulting in transcription activation.[3]

（酸感应原理图）

To test the idea that P170 is sensitive to acidity under the regulation of RcfB, we construct RFP gene into circuit containing P170 and RcfB. The RFP is expressed on the basis of P170 activation and RcfB which functions as a novel regulatory protein however, is controlled by a constitutive promoter J23100. High level of P170 activity required both RcfB and acidic conditions. Therefore, with the constitutive expression of RcfB, once the pH reaches the threshold that usually ranges from pH 6.0 to pH 6.5, P170 will be induced so that RFP can reflect red fluorescence under UV detection. Although RFP verification test is well developed, other functional genes are also replace RFP gene as a strategy for application extension. In our later experiment, we substitute RFP for T7 polymerase for regulatory purpose.

（模块图）

4.2 Regulating

After activated sensing system which determines the pH threshold to suppress bacterial population density, we need to figure out how to retrieve to the proper acidity for living. Here comes our regulating system for acid recovery.

The ssrA tag sequence (mf-ssrA tag) and the Lon protease (mf-Lon) from Mesoplasma florum are made up of the crucial elements of a protein degradation system. Experiments has been identified that mf-ssrA tag is efficiently recognized by mf-Lon where the tag appends to C terminus of native or denatured proteins resulted in their rapid proteolysis by mf-Lon.[4] Besides, degradation system based on the Gram-positive M. florum tmRNA system does not rely on host degradation systems and can function in a wide range of bacteria, which makes it an adaptive method in variety. Here, we use this proteolysis system for lactate regulation and keep it in a oscillatory value of acidity.

Specifically, we utilize the effect of mf-Lon as well as ldhE bearing with tag under the control T7 promoter and J2310 promoter respectively, to degrade the overmuch lactate. We also aware that T7 promoter activation requires the combination of T7 RNA polymerase which is extremely promoter-specific and transcribes only DNA downstream of a T7 promoter.[5] According to the extensive study of our ‘sensing’ system, we substitute the RFP for T7 polymerase hoping that lower pH stage can activate T7 polymerase activation which then combines with T7 promoter for acting and mf-Lon, in this way, also expresses. It turns out that ldhE tethered with mf-ssrA tag can be degraded by cytoplasmic mf-Lon. So the pH can maintain in a proper level for cells’ living.

（模块图）（实验表征结果和说明）

Notably, the proteolysis system has potential to apply in many fields. As a strategy to make it a toolbox for further research, we use different tags to test the strength of its proteolysis. With the reflection of red fluorescence, we are able to detect mf-Lon activity on various tags based on the distinguish value of UV detection. This toolbox is intended to be a fast and convenient method for prospective proteolysis option and degradation research.

（不同tag模块图）（实验表征结果和说明）

References

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[1] Min C, Chung H, Choi W, et al. Linear correlation between inactivation of E. coli and OH radical concentration in TiO2 photocatalytic disinfection.[J]. Water Research, 2004, 38(4):1069–1077. [2] Madsen S M, Arnau J, Vrang A, et al. Molecular characterization of the pH-inducible and growth phase-dependent promoter P170 of Lactococcus lactis.[J]. Molecular Microbiology, 1999, 32(1):75-87.
[3] Madsen, Søren M, Hindré, Thomas, Le Pennec, Jean‐Paul, et al. Two acid‐inducible promoters from Lactococcus lactis require the cis‐acting ACiD‐box and the transcription regulator RcfB[J]. Molecular Microbiology, 2005, 56(3):735-746.
[4] Eyal G, Sauer R T. Evolution of the ssrA degradation tag in Mycoplasma: specificity switch to a different protease.[J]. Proceedings of the National Academy of Sciences, 2008, 105(42):16113-16118.
[5] Martin C T, Esposito E A, Theis K, et al. Structure and function in promoter escape by T7 RNA polymerase.[J]. Prog Nucleic Acid Res Mol Biol, 2005, 80(80):323–347.

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