Difference between revisions of "Part:BBa K206000"

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	===Functional Parameters===		===Functional Parameters===
	<partinfo>BBa_K206000 parameters</partinfo>		<partinfo>BBa_K206000 parameters</partinfo>
		+	<!-- -->
		+
		+	== Characterized by BNU-China 2019 ==
		+
		+	We characterize pBAD (BBa_K206000) by an induced suicide system, in which pBAD controls the downstream mazF (BBa_K302033) gene that serves as a reporter, which encodes an endoribonuclease that cleaves RNAs at ACA sites and causes the death of microbe [1]. As a result, we can characterize pBAD in a cell density-dependent manner in Escherichia coli K-12.
		+
		+	[[Image:2019 BNU-China BBa K3036005 change.png| border | center | 400px]]<br>
		+
		+	In order to characterize pBAD induced by L-arabinose under different concentrations, we take engineered microbe without induction as control group.
		+
		+	As is shown in Fig.1, the cell number of experimental groups show a significant decrease, which indicates pBAD can be induced by 1.25μM/L and 2.5μM/L arabinose, and 2.5μM/L can be considered as a more effective concentration.
		+
		+	[[Image:2019 BNU-China BBa K302033 change.jpg| border | center | 400px]]<br>
		+
		+	Figure 1 Cell number declines after induction by L-arabinose. It proves that pBAD is induced by L-arabinose.
		+
		+	Beyond our project, pBAD is applied for heterologous gene expression due to its advantages, including moderately high expression levels, induction by a low-cost and non-toxic monosaccharide L-arabinose and tight regulation of transcription, which is particularly significant to expressing toxins. [2]
		+
		+	<b>Experimental approach</b>
		+
		+	1. Transform the plasmids into E. coli DH5α competent cells.
		+	2. The engineered bacteria are cultured in 200mL LB-ampicillin (50 ng/µl) medium overnight at 37℃, 200rpm;
		+	3. Equally divide the culture into 90 centrifuge tubes, which is 1mL respectively. Centrifuge them at 4000rpm for 5 minutes. Discard the liquid.
		+	4. Resuspend 30 tubes of collected bacteria with LB-ampicillin (50 ng/µl) containing 1.25μM/L and 2.5μM/L L-arabinose respectively as experimental groups. Resuspend 30 tubes of bacteria with pure LB-ampicillin (50 ng/µl) medium.
		+	5. Collect 3 tubes of all groups every 6 hours, dilute all of the samples to 107 times and then spread them on solid LB-ampicillin (50 ng/µl) medium separately. At the same time, refresh the medium to maintain the concentration of L-arabinose.
		+	6. Count the number of colonies in 5 cm2 per plate after cultured for 24 hours at 37℃
		+	7. Three repicas are tested in each group.
		+
		+	<b>Reference</b>
		+
		+	[1] Nigam A, Ziv T, Oron-Gottesman A, Engelberg-Kulka H2019. Stress-induced MazF-mediated proteins in Escherichia coli. mBio 10: e00340-19. doi:10.1128/mBio.00340-19.
		+	[2] Diana Széliová, Ján Krahulec, Martin Šafránek, et al. Modulation of heterologous expression from PBAD promoter in Escherichia coli production strains[J]. Journal of Biotechnology, 2016, 236:1-9.
		+
		+
		+	<!-- Add more about the biology of this part here
		+	===Usage and Biology===
		+
		+	<!-- -->
		+	<span class='h3bb'>Sequence and Features</span>
		+	<partinfo>BBa_K654059 SequenceAndFeatures</partinfo>
		+
		+
		+	<!-- Uncomment this to enable Functional Parameter display
		+	===Functional Parameters===
		+	<partinfo>BBa_K654059 parameters</partinfo>
	<!-- -->		<!-- -->

---

Latest revision as of 14:17, 16 October 2019

Name: pBAD strong Input: [http://openwetware.org/wiki/Arabinose L-arabinose] Output: PoPS Part Main Page        Part Design        Characterization        Family        Add Data

Usage and Biology

pBAD is an E.coli promoter that is induced by L-arabinose. In the absence of arabinose, the repressor protein AraC (BBa_I13458) binds to the AraI1 operator site of pBAD and the upstream operator site AraO2, blocking transcription [1]. In the presence of arabinose, AraC binds to it and changes its conformation such that it interacts with the AraI1 and AraI2 operator sites, permitting transcription [1].

K206000 is a variant pBAD promoter with a modified AraI1 site that has been shown both to be responsive to lower concentrations of arabinose and to exhibit a higher maximum expression than the wild type (BBa_I13453), as measured by coupling to a fluorescent reporter.

What you can do with it:
At a given level of arabinose input, BBa_K206000 will provide a higher level of PoPS output than its family members, allowing analog device responses. See [http://2009.igem.org/Team:British_Columbia our wiki] for a project that makes use of this property.

Compatibility:
Chassis: Best used in the E. coli strain [http://cgsc.biology.yale.edu/Strain.php?ID=111773 BW27783], which has been modified to permit homogeneous pBAD promoter expression by substituting the chromosomal arabinose-dependent promoter of AraE (arabinose transporter protein) with a constitutive promoter [2].
Backbone: Has been shown to work on plasmid pSB1C3.
Reporter: Has been shown to work with reporters BBa_I13507 and BBa_I763020.

Sequence and Features

References

[http://www.ncbi.nlm.nih.gov/pubmed/11102706 [1]] Schlief, R. (2000). Regulation of the L-arabinose operon of Escherichia coli. Trends in Genetics. 16(12):559-565.
[http://www.ncbi.nlm.nih.gov/pubmed/11739756 [2]] Khlebnikov A, Datsenko KA, Skaug T, Wanner BL, and Keasling JD. (2001). Homogeneous expression of the PBAD promoter in Escherichia coli by constitutive expression of the low-affinity high-capacity AraE transporter. Microbiology. 147(12):3241-7.

Characterized by BNU-China 2019

We characterize pBAD (BBa_K206000) by an induced suicide system, in which pBAD controls the downstream mazF (BBa_K302033) gene that serves as a reporter, which encodes an endoribonuclease that cleaves RNAs at ACA sites and causes the death of microbe [1]. As a result, we can characterize pBAD in a cell density-dependent manner in Escherichia coli K-12.

In order to characterize pBAD induced by L-arabinose under different concentrations, we take engineered microbe without induction as control group.

As is shown in Fig.1, the cell number of experimental groups show a significant decrease, which indicates pBAD can be induced by 1.25μM/L and 2.5μM/L arabinose, and 2.5μM/L can be considered as a more effective concentration.

Figure 1 Cell number declines after induction by L-arabinose. It proves that pBAD is induced by L-arabinose.

Beyond our project, pBAD is applied for heterologous gene expression due to its advantages, including moderately high expression levels, induction by a low-cost and non-toxic monosaccharide L-arabinose and tight regulation of transcription, which is particularly significant to expressing toxins. [2]

Experimental approach

1. Transform the plasmids into E. coli DH5α competent cells. 2. The engineered bacteria are cultured in 200mL LB-ampicillin (50 ng/µl) medium overnight at 37℃, 200rpm; 3. Equally divide the culture into 90 centrifuge tubes, which is 1mL respectively. Centrifuge them at 4000rpm for 5 minutes. Discard the liquid. 4. Resuspend 30 tubes of collected bacteria with LB-ampicillin (50 ng/µl) containing 1.25μM/L and 2.5μM/L L-arabinose respectively as experimental groups. Resuspend 30 tubes of bacteria with pure LB-ampicillin (50 ng/µl) medium. 5. Collect 3 tubes of all groups every 6 hours, dilute all of the samples to 107 times and then spread them on solid LB-ampicillin (50 ng/µl) medium separately. At the same time, refresh the medium to maintain the concentration of L-arabinose. 6. Count the number of colonies in 5 cm2 per plate after cultured for 24 hours at 37℃ 7. Three repicas are tested in each group.

Reference

[1] Nigam A, Ziv T, Oron-Gottesman A, Engelberg-Kulka H2019. Stress-induced MazF-mediated proteins in Escherichia coli. mBio 10: e00340-19. doi:10.1128/mBio.00340-19. [2] Diana Széliová, Ján Krahulec, Martin Šafránek, et al. Modulation of heterologous expression from PBAD promoter in Escherichia coli production strains[J]. Journal of Biotechnology, 2016, 236:1-9.

Sequence and Features