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| <h4 id="overviewoncaulobactercrescentus">Overview on Caulobacter crescentus</h4> | | <h4 id="overviewoncaulobactercrescentus">Overview on Caulobacter crescentus</h4> |
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- | <p>Caulobacter crescentus is a kind of bacteria with many necessity for our project: <i>C.crescentus</i> has a special life cycle, including swarmed period when <i>C.crescentus</i> possesses flagellum in one pole and stalked period when bacteria cut up flagellum and develop an extremely strong polar adhesive envelope structure known as the holdfast which is composed of protein and polysaccharide. According to the research, when holdfast cling to a surface, the force on it reaches 68 N/mm2 high,which is regarded as the most strongest biological glue known to exist in nature and is three times strong as commercial 'super glue'. With the knowledge we have already known, if we are able to regulate the biosynthesis of flagellum and holdfast simultaneously with flourescent proteins controlled by light input, <i>C.crescentus</i> will stop swimming, develop holdfast to stay firmly and evenly on the plate with expressing flourescent proteins corresponding to light color simulation.<p/> | + | <p>Caulobacter crescentus is a kind of bacteria with many necessity for our project: <i>C.crescentus</i> has a special life cycle, including swarmed period when <i>C.crescentus</i> possesses flagellum in one pole and stalked period when they cut up flagellum and develop an extremely strong polar adhesive envelope structure known as the holdfast which is composed of protein and polysaccharide. According to the research, when a holdfast clings to a surface, the force on it reaches 68 N/mm2 high, which is regarded as the strongest biological glue known to exist in nature and is three times stronger as commercial 'super glue'. With the knowledge we have already known, if we are able to regulate the biosynthesis of flagellum and holdfast simultaneously with flourescent proteins controlled by light input, <i>C.crescentus</i> will stop swimming, develop holdfast to stay firmly and evenly on the plate while expressing flourescent proteins corresponding to light color simulation.<p/> |
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| <p><img src="https://static.igem.org/mediawiki/2014/9/98/Caulo3.png" class="th"/></p> | | <p><img src="https://static.igem.org/mediawiki/2014/9/98/Caulo3.png" class="th"/></p> |
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| <p>In order to realize the blueprint of our design, we have these works to do as following: <p/> | | <p>In order to realize the blueprint of our design, we have these works to do as following: <p/> |
- | <p>1. Figure out the exact proteins regulating the biosynthesis of flagellum and holdfast or keeping bacteria staying in a place relatively and then construct a circuit which contains controlling proteins triggered or inhibited by light signal.<p/> | + | <ol> |
- | <p>2. Discover some methods to guide accomplished light sensing-imaging systems working in <i>E. coli</i> into C.crescentus. <p/> | + | <li>Figure out the exact proteins regulating the biosynthesis of flagellum and holdfast or keeping bacteria staying in a relatively narrow place and then construct a circuit which contains controlling proteins triggered or inhibited by light signal.</li> |
- | <p>3. Confirm the exact nutrition conditions for an even <i>C.crescentus</i> biofilm genesis with modeling work and lab tests.<p/> | + | <li>Discover some methods to transfer accomplished light sensing-imaging systems working in <i>E. coli</i> into C.crescentus. </li> |
| + | <li>Confirm the exact nutrition conditions for an even <i>C.crescentus</i> biofilm genesis with modeling work and lab tests.<br/> |
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- | <p>Here, we are attempting to introduce the whole view of this amazing bacteria for you to be better understanding our project and its specialty. <p/> | + | </ol> |
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| + | <p>Here, we are attempting to introduce the whole view of this amazing bacteria for you to better understande our project and its specialty. <p/> |
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| <h4 id="lifecycleandnutritionalprovide">Life Cycle and Nutritional Provide</h4> | | <h4 id="lifecycleandnutritionalprovide">Life Cycle and Nutritional Provide</h4> |
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- | <p>The cyclic developmental program of <em>Caulobacter crescentus</em> starts with a stalked cell with a polar adhesive holdfast at the tip of the holdfast. The stalked cell firstly turns into S phase when it is time for DNA replication. At that time, the bacteria grow up into pre-divisional cells. Later the cell enters the G2 phase when the cell becomes incompetent for DNA replication and it keep growing until finally compartmentalizing into two cells, either of who contains stalk and flagellum in one pole. For the swarmer cell which possesses flagellum, the rotation of flagellum is activated and two pili are generated as well. The swarmer one enters G1 phase when its chromosome is different from the stalked one and it cannot reproduce itself. However, in G1 phase, the holdfast is formed predominantly in the swarmer cell stage and these swarmer cells reenter S phase like a cell differentiation process exactly simultaneously when rotating flagellum disappears and holdfast is synthesized. <p/> | + | <p>The cyclic developmental program of <em>Caulobacter crescentus</em> starts with a stalked cell with a polar adhesive holdfast at the tip of the stalk. The stalked cell firstly turns into S phase when it is time for DNA replication. At that time, the bacteria grow up into pre-divisional cells. Later the cell enters the G2 phase when the cell becomes incompetent for DNA replication and it keep growing until finally compartmentalizing into two cells, either of who contains stalk and flagellum in one pole. For the swarmer cell which possesses flagellum, the rotation of flagellum is activated and two pili are generated as well. The swarmer one enters <i>G1</i> phase when its chromosome is different from the stalked one and it cannot reproduce itself. However, in <i>G1</i> phase, the holdfast is formed predominantly in the swarmer cell stage and these swarmer cells reenter S phase like a cell differentiation process exactly simultaneously when rotating flagellum disappears and holdfast is synthesized. As the research says, the development of stalk and holdfast help <em>C.crescentus</em> to live in some tough surroundings and enhance its ability to absorb phosphate passively when nutrition provide is limited and swimming using flagellum waste the energy that is original manuscript for necessary metabolism. Scientists found that <i>Pst</i> family correlate the length of stalk. As the hypothesis contains, if it is correct, stalk elongation may function to elevate single cell away from surface thus bacteria receive much high-level nutrient flux and if <em>C.crescentus</em> colonize with other organisms, stalk ensures bacteria to have greater access to nutrients comparing to other nearby surface species to be superior in competition and survival. Consequently, C.crescentus is able to survive without flagellum and even much more stronger when containing holdfast.<p/> |
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| <p><img src="https://static.igem.org/mediawiki/2014/0/06/Life_cycle_of_cc.png" class="th"/></p> | | <p><img src="https://static.igem.org/mediawiki/2014/0/06/Life_cycle_of_cc.png" class="th"/></p> |
- | <p>As the research says, the development of stalk and holdfast helps <em>C.crescentus</em> to live in some tough surroundings and enhance its ability to absorb phosphate passively when nutrition provide is limited and swimming using flagellum waste the energy that is original manuscript for necessary metabolism. Scientists found that Pst family correlate the length of stalk. As the hypothesis contains, if it is correct, stalk elongation may function to elevate single cell away from surface thus bacteria receive much high-level nutrient flux and if <em>C.crescentus</em> colonize with other organisms, stalk ensures bacteria to have greater access to nutrients comparing to other nearby surface species to be superior in competition and survival. Consequently, C.crescentus is able to survive withour flagellum and even much more stronger when containing holdfast.<p/>
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- | <p><img src="https://static.igem.org/mediawiki/2014/9/93/C.c_holdfast_function.jpg" class="th"/></p>
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- | <p>In accordance with recent research, many kinds of protein are assistedly, antagonistically or stimulatively working for a distinct process during the life cycle of <em>C.crescentus</em> such as RodA and MreB are required for stalk synthesis and prevetion of ectopic pole formation, PodJ is an organelle development protin that differentailly localized and required for polar targeting on PleC development regulator,sigma-factor is also required for polar morphogensis and normal celldivision, BapE DNA endonuclease induces an apoptotic-like response to DNA damage whichis useful for future kill switch design and SpmX localizaion relates to stalk position not only working in <em>C.crescentus</em>, but in <em>A.xcentricus</em> and <em>A.biprosthecum</em> etc. <p/> | + | <p>In accordance with recent research, many kinds of proteins are assistedly, antagonistically or stimulatively working for a distinct process during the life cycle of <em>C.crescentus</em> such as RodA and MreB are required for stalk synthesis and prevetion of ectopic pole formation, PodJ is an organelle development protein that differently localized and required for polar targeting on PleC development regulator, sigma-factor is also required for polar morphogensis and normal celldivision, BapE DNA endonuclease induces an apoptotic-like response to DNA damage which is useful for future kill switch design and SpmX localizaion relates to stalk position not only working in <em>C.crescentus</em>, but in <em>A.xcentricus</em> and <em>A.biprosthecum</em> etc. <p/> |
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| <p>In the whole life cycle of <em>C.crescentus</em>, we mostly focus on the process of degradation of flagellum and biosynthesis of holdfast. Thus, we will discuss the pathway of the two parts dividedly and design a reasonable circuit containing protein involved the pathway controlled by light signals. <p/> | | <p>In the whole life cycle of <em>C.crescentus</em>, we mostly focus on the process of degradation of flagellum and biosynthesis of holdfast. Thus, we will discuss the pathway of the two parts dividedly and design a reasonable circuit containing protein involved the pathway controlled by light signals. <p/> |
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| <h4 id="dgradgrb">DgrA/DgrB</h4> | | <h4 id="dgradgrb">DgrA/DgrB</h4> |
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- | <p>The concentration of <i>c-di-GMP</i> is varying, and for our experiment we will promote its expression to inhibit rotation of flagella. It will bind to <i>DgrA</i> and <i>DgrB</i>. The resulting complex will have two routes to go: one is the [<i>c-di-GMP&</i>;<i>DgrA</i>] complex which will inhibit <i>FliL</i>, a protein bound to the membrane playing a key role in rotation of flagella. And the other route is that the <i>DgrB</i> will directly affect the rotation of the flagella.</p> | + | <p>The concentration of <i>c-di-GMP</i> is varying, and for our experiment we will promote its expression to inhibit rotation of flagella. It will bind to <i>DgrA</i> and <i>DgrB</i>. The resulting complex will have two routes to go: one is the [<i>c-di-GMP&</i>;<i>DgrA</i>] complex which will inhibit <i>FliL</i>, a protein bounds to the membrane playing a key role in rotation of flagella. The other route is that the <i>DgrB</i> will directly affect the rotation of the flagella.</p> |
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- | <h4 id="hf"><i>HfiA/HfsJ</i></h4> | + | <h4 id="hf">HfiA/HfsJ</h4> |
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| <p><i>Ref: A Cell Cycle and Nutritional Checkpoint Controlling Bacterial Surface Adhesion</i></p> | | <p><i>Ref: A Cell Cycle and Nutritional Checkpoint Controlling Bacterial Surface Adhesion</i></p> |
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| <p>In this paper, author describes a novel regulatory mechanism by which the <i>C.c.</i> bacterium integrates cell cycle and nutritional signals to control development of an adhesive envelop structure known as holdfast.</p> | | <p>In this paper, author describes a novel regulatory mechanism by which the <i>C.c.</i> bacterium integrates cell cycle and nutritional signals to control development of an adhesive envelop structure known as holdfast.</p> |
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- | <p>They discovered a novel inhibitor of holdfast development. <i>HfiA</i>, that is regulated downstream of <i>lovK-lovR</i>. They also discovered a bio-synthesis related gene named <i>HfsJ</i>. And the suppressing mutations in HfsJ attenuate the <i>HfsJ-HfiA</i> interaction.</p> | + | <p>They discovered a novel inhibitor of holdfast development. <i>HfiA</i>, that is regulated downstream of <i>lovK-lovR</i>. They also discovered a bio-synthesis related gene named <i>HfsJ</i>. The suppressing mutations in HfsJ attenuate the <i>HfsJ-HfiA</i> interaction.</p> |
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| <p><img src="https://static.igem.org/mediawiki/2014/9/9e/Holdfast.png" class="th"/></p> | | <p><img src="https://static.igem.org/mediawiki/2014/9/9e/Holdfast.png" class="th"/></p> |
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- | <p>These results support a model in which <i>HfiA</i> inhibits holdfast development via direct interaction with an enzyme required for holdfast biosynthesis</p> | + | <p>These results support a model in which <i>HfiA</i> inhibits holdfast development via direct interaction with an enzyme required for holdfast bio-synthesis</p> |
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| <p>In conclusion, author says: We demonstrate that the predicted glycosyltransferase, <i>HfsJ</i>, is a required component of the holdfast development machinery and that residues at the C-terminus of <i>HsfJ</i> mediate a direct interaction with <i>HfiA</i>, leading to a post-translational inhibition of <i>HfsJ</i>.</p> | | <p>In conclusion, author says: We demonstrate that the predicted glycosyltransferase, <i>HfsJ</i>, is a required component of the holdfast development machinery and that residues at the C-terminus of <i>HsfJ</i> mediate a direct interaction with <i>HfiA</i>, leading to a post-translational inhibition of <i>HfsJ</i>.</p> |