Team:Peking/Notebook/Vocabulary

From 2010.igem.org

(Difference between revisions)
(TPS)
 
(30 intermediate revisions not shown)
Line 4: Line 4:
<div id="tgreen">
<div id="tgreen">
<br><br>
<br><br>
-
<font size=10><font color=#585858><font face="Franklin Gothic Demi Cond">&nbsp;&nbsp;&nbsp;Protocols</font></font></font>
+
<font size=10><font color=#585858><font face="Franklin Gothic Demi Cond">&nbsp;&nbsp;&nbsp;Vocabulary</font></font></font>
<br><br><br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<font color=#ffffff></html
<br><br><br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<font color=#ffffff></html
Line 14: Line 14:
<br><br>
<br><br>
<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
-
<font size=5><b><font color=#74DF00>Protocols of Experiment Ver.2010</font></font></b>
+
<font size=5><b><font color=#74DF00>Vocabulary of Peking iGEM 2010</font></font></b>
</div>
</div>
-
<div id="middlegreen">
+
<div id="middlegreen"><font color=#ffffff>
</html>
</html>
-
==Peking 2010 team==
+
==Vocabulary==
-
<html>
+
===Antigen 43===
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
'''Antigen 43''' is a unique autotransporter that promote bacterial cell-to-cell aggregation. Antigen 43 can be expressed on the E.coli cell surface in large quantities, up to 50000 copies per cell.[1] The structure analysis of antigen 43 revealed that antigen 43 has an N-terminal signal peptide; an N-proximal passenger domain that is secreted, which could also be called α domain; an autochaperone domain that facilitates folding of the passenger domain; and a C-terminal β-barrel domain that forms an integral outer membrane protein, also called β domain[2]. The passenger domain(αdomain) confers the autoaggregation phenotype and it is bound to the surface via non-covalent interaction with the βdomain.
-
<a href="https://2010.igem.org/Team:Peking/Notebook/Protocols/SDS&WB"><font size=3><font color=#FFFFFF>*SDS-PAGE & western blot protocol</font></font></a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="https://static.igem.org/mediawiki/2010/7/7e/SDS-PAGE_%26_western_blot_protocol.pdf"target="blank"><img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>download PDF version</a><br>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
<html><img src="http://partsregistry.org/wiki/images/0/0f/Antigen431.jpg" width=400 id="imggreen"></html><br>
-
<a href="https://2010.igem.org/Team:Peking/Notebook/Protocols/SDS&W"><font size=3><font color=#FFFFFF>*SDS-PAGE & western sample preparation protocol</font></font></a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="https://static.igem.org/mediawiki/2010/f/f8/SDS-PAGE_%26_western_sample_preparation_protocol-xteng.pdf"target="blank"><img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>download PDF version</a><br>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
The structure of the coding sequence of antigen 43. Antigen 43 contains a signal peptide, a passenger domain, an autochaperone domain and a translocation unit, which are all indicated in this figure.
-
<a href="https://2010.igem.org/Team:Peking/Notebook/Protocols/MBP"><font size=3><font color=#FFFFFF>*Protocol for chemical inducible expression of MBP & sample preparation</font></font></a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="https://static.igem.org/mediawiki/2010/0/08/Protocol_for_chemical_inducible_expression_of_MBP_%26_sample_preparation.pdf" target="blank"><img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>download PDF version</a><br>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
===MerR===
-
<a href="https://2010.igem.org/Team:Peking/Notebook/Protocols/DDDP"><font size=3><font color=#FFFFFF>*DNA Double Digestion Protocol</font></font></a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
'''MerR''', the eponymous and first identified member of the merR family, can bind mercury ions directly and regulates expression of bacterial mercury ion resistance operons.
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="https://static.igem.org/mediawiki/2010/8/84/DNA_double_digestion_protocol.pdf"target="blank"><img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>download PDF version</a><br>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
===MBP===
-
<a href="https://2010.igem.org/Team:Peking/Notebook/Protocols/DGEP"><font size=3><font color=#FFFFFF>*DNA Gel Extraction Protocol</font></font></a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
'''MBP''', a kind of mercury mental binding peptide that consists of two tandemed copies of metal binding domain of MerR including dimerization helix and metal binding loop together
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="https://static.igem.org/mediawiki/2010/8/83/DNA_Gel_extraction_protocol.pdf"target="blank"><img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>download PDF version</a><br>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
===DsbA===
-
<a href="https://2010.igem.org/Team:Peking/Notebook/Protocols/MP"><font size=3><font color=#FFFFFF>*Miniprep Protocol</font></font></a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
'''DsbA (a periplasmic disulfide bond oxidoreductase)''',a SecA dependent signal protein , can export its C-terminal fusion protein into periplasm on the signal recognition particle (SRP) pathway
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="https://static.igem.org/mediawiki/2010/1/19/Miniprep_Protocol.pdf"target="blank"><img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>download PDF version</a><br>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
===ICP-AES===
-
<a href="https://2010.igem.org/Team:Peking/Notebook/Protocols/PCIEG"><font size=3><font color=#FFFFFF>*Protocol for Chemical Inducible Expression of GFP</font></font></a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
'''Inductively Coupled Plasma Atomic Emission Spectrometry: (ICP-AES)''', also referred to as inductively coupled plasma optical emission spectrometry (ICP-OES), is an analytical technique used for the detection of trace metals. It is a type of emission spectroscopy that uses the inductively coupled plasma to produce excited atoms and ions that emit electromagnetic radiation at wavelengths characteristic of a particular element. The intensity of this emission is indicative of the concentration of the element within the sample.(Wikipedia)
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="https://static.igem.org/mediawiki/2010/0/06/Protocol_for_chemical_inducible_expression_of_GFP.pdf"target="blank"><img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>download PDF version</a><br>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
===LOM===
-
<a href="https://2010.igem.org/Team:Peking/Notebook/Protocols/PDPRM"><font size=3><font color=#FFFFFF>*Protocol for DNA Purification from Reaction Mixture</font></font></a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
'''LOM (lpp-OmpA-MBP)''', a fusion protein consists of first 9 amino acids of lipoprotein, residues 46~159 of OmpA, an outer membrane protein and our lead binding peptide,MBP.
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="https://static.igem.org/mediawiki/2010/b/bf/Protocol_for_DNA_purification_from_reaction_mixture.pdf"target="blank"><img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>download PDF version</a><br>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
===PAN===
-
<a href="https://2010.igem.org/Team:Peking/Notebook/Protocols/PLIDPVD"><font size=3><font color=#FFFFFF>*Protocol for Ligation of Insert DNA into Plasmid Vector DNA</font></font></a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
'''1-(2-Pyridylazo)-2-naphthol'''
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="https://static.igem.org/mediawiki/2010/0/04/Protocol_for_ligation_of_insert_DNA_into.pdf"target="blank"><img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>download PDF version</a><br>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
Molecular Structure  <html><a href="https://static.igem.org/mediawiki/2010/2/2f/Pppku.jpg" target="blank"><img src="https://static.igem.org/mediawiki/2010/2/2f/Pppku.jpg"></a></html>
-
<font size=3><font color=#FFFFFF>*Protocol for PCR with EasyPfu DNA Polymerase Preparation for Reaction</font></font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="https://static.igem.org/mediawiki/2010/d/da/Protocol_for_PCR_with_EasyPfu_DNA_Polymerase_Preparation_for_Reaction_Mixture.pdf"target="blank"><img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>download PDF version</a><br>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
Molecular Formula      C15H11N3O
-
<a href="https://2010.igem.org/Team:Peking/Notebook/Protocols/PPCCT"><font size=3><font color=#FFFFFF>*Protocol for Preparation of Competent Cells for Transformation</font></font></a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="https://static.igem.org/mediawiki/2010/4/43/Protocol_for_preparation_of_competent_cells_for_transformation.pdf"target="blank"><img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>download PDF version</a><br>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
Molecular Weight        249.27
-
<a href="https://2010.igem.org/Team:Peking/Notebook/Protocols/SDMP"><font size=3><font color=#FFFFFF>*Site-directed Mutagenesis Protocol</font></font></a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="https://static.igem.org/mediawiki/2010/d/d0/Site_directed_mutagenesis_protocol.pdf"target="blank"><img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>download PDF version</a><br>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
CAS Registry Number    85-85-8
-
<a href="https://2010.igem.org/Team:Peking/Notebook/Protocols/TP"><font size=3><font color=#FFFFFF>*Transformation Protocol</font></font></a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="https://static.igem.org/mediawiki/2010/7/75/Transformation_protocol.pdf"target="blank"><img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>download PDF version</a><br>
+
-
<br><br>
+
EINECS                201-637-9
-
</div>
+
Melting point          134-141 ºC
-
<div id="notebook home">
+
-
<div id="titlegreen">
+
-
<br><br>
+
-
<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<font size=5><b><font color=#74DF00>Protocols of Experiment Ver.2009</font></font></b>
+
-
</div>
+
-
<div id="middlegreen">
+
Water solubility        Insoluble
-
</html>
+
-
==Peking 2009 team==
+
===PbrR===
-
<html>
+
'''PbrR''', the other member of the merR family, can bind lead ions directly and regulates expression of bacterial lead ion resistance operons.
 +
===Reverse engineering===
 +
'''Reverse engineering''' is the process of discovering the technological principles of a device, object or system through analysis of its structure, function and operation. It often involves taking something apart and analyzing its workings in detail to be used in maintenance, or to try to make a new device or program that does the same thing without using or simply duplicating (without understanding) any part of the original. (Wikipedia)
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
===TPS===
-
<img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>
+
'''TritonX-100-PAN-S''' :A self-synthesized  water-soluble metal indicator with colorimetric selectivity for heavy metals.
-
<a href="https://static.igem.org/mediawiki/2009/0/00/PKU_Miniprep_Protocol.pdf"target="blank"><font size=3><font color=#FFFFFF>Miniprep Protocol</font></font></a>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>
+
-
<a href="https://static.igem.org/mediawiki/2009/8/85/PKU_DNA_Gel_extraction_protocol.pdf"target="blank"><font size=3><font color=#FFFFFF>DNA Gel Extraction Protocol</font></font></a>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>
+
-
<a href="https://static.igem.org/mediawiki/2009/1/1d/PKU_DNA_digestion_protocol.pdf"target="blank"><font size=3><font color=#FFFFFF>DNA Double Digestion Protocol</font></font></a>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>
+
-
<a href="https://static.igem.org/mediawiki/2009/4/46/PKU_Protocol_for_DNA_purification_from_reaction_mixture.pdf"target="blank"><font size=3><font color=#FFFFFF>Protocol for DNA Purification From Reaction Mixture</font></font></a>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>
+
-
<a href="https://static.igem.org/mediawiki/2009/6/61/PKU_Protocol_for_ligation_of_insert_DNA_into_plasmid_vector_DNA.pdf"target="blank"><font size=3><font color=#FFFFFF>Ligation of Inserting DNA into Plasmid Vector DNA</font></font></a>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>
+
-
<a href="https://static.igem.org/mediawiki/2009/d/da/PKU_Protocol_for_PCR_with_EasyPfu_DNA_Polymerase.pdf"target="blank"><font size=3><font color=#FFFFFF>Protocol for PCR with EasyPfu DNA Polymerase</font></font></a>
+
-
 
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>
+
-
<a href="https://static.igem.org/mediawiki/2009/b/ba/PKU_Protocol_for_preparation_of_competent_cells_for_transformation.pdf"target="blank"><font size=3><font color=#FFFFFF>Protocol for preparation of competent cells for transformation</font></font></a>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>
+
-
<a href="https://static.igem.org/mediawiki/2009/6/6f/PKU_Site-directed_mutagenesis_protocol.pdf"target="blank"><font size=3><font color=#FFFFFF>Site-directed mutagenesis protocol</font></font></a>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>
+
-
<a href="https://static.igem.org/mediawiki/2009/1/11/PKU_Transformation_protocol.pdf"target="blank"><font size=3><font color=#FFFFFF>Transformation Protocol</font></font></a>
+
-
<br>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+
-
<img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>
+
-
<a href="https://static.igem.org/mediawiki/2009/1/13/PKU_Protocol_for_chemical_inducible_expression_of_GFP.pdf"target="blank"><font size=3><font color=#FFFFFF>Protocol for Chemical Inducible Expression of GFP</font></font></a>
+
 +
===Traffic light bioassay===
 +
'''Traffic light bioassay''', the assay we have designed utilized similar indications as road signal for directing vehicular traffic by means of colored lights when we expect that several shades of blue imply different concentrations of heavy metal ions detected.
 +
 +
<html>
 +
</font>
</div>
</div>
-
 
-
 
<div id="project description bottom">
<div id="project description bottom">
<div id="bottomgreen">
<div id="bottomgreen">

Latest revision as of 20:28, 27 October 2010




   Vocabulary


        Notebook > Vocabulary


      Vocabulary of Peking iGEM 2010

Contents

Vocabulary

Antigen 43

Antigen 43 is a unique autotransporter that promote bacterial cell-to-cell aggregation. Antigen 43 can be expressed on the E.coli cell surface in large quantities, up to 50000 copies per cell.[1] The structure analysis of antigen 43 revealed that antigen 43 has an N-terminal signal peptide; an N-proximal passenger domain that is secreted, which could also be called α domain; an autochaperone domain that facilitates folding of the passenger domain; and a C-terminal β-barrel domain that forms an integral outer membrane protein, also called β domain[2]. The passenger domain(αdomain) confers the autoaggregation phenotype and it is bound to the surface via non-covalent interaction with the βdomain.


The structure of the coding sequence of antigen 43. Antigen 43 contains a signal peptide, a passenger domain, an autochaperone domain and a translocation unit, which are all indicated in this figure.

MerR

MerR, the eponymous and first identified member of the merR family, can bind mercury ions directly and regulates expression of bacterial mercury ion resistance operons.

MBP

MBP, a kind of mercury mental binding peptide that consists of two tandemed copies of metal binding domain of MerR including dimerization helix and metal binding loop together

DsbA

DsbA (a periplasmic disulfide bond oxidoreductase),a SecA dependent signal protein , can export its C-terminal fusion protein into periplasm on the signal recognition particle (SRP) pathway

ICP-AES

Inductively Coupled Plasma Atomic Emission Spectrometry: (ICP-AES), also referred to as inductively coupled plasma optical emission spectrometry (ICP-OES), is an analytical technique used for the detection of trace metals. It is a type of emission spectroscopy that uses the inductively coupled plasma to produce excited atoms and ions that emit electromagnetic radiation at wavelengths characteristic of a particular element. The intensity of this emission is indicative of the concentration of the element within the sample.(Wikipedia)

LOM

LOM (lpp-OmpA-MBP), a fusion protein consists of first 9 amino acids of lipoprotein, residues 46~159 of OmpA, an outer membrane protein and our lead binding peptide,MBP.

PAN

1-(2-Pyridylazo)-2-naphthol

Molecular Structure

Molecular Formula C15H11N3O

Molecular Weight 249.27

CAS Registry Number 85-85-8

EINECS 201-637-9

Melting point 134-141 ºC

Water solubility Insoluble

PbrR

PbrR, the other member of the merR family, can bind lead ions directly and regulates expression of bacterial lead ion resistance operons.

Reverse engineering

Reverse engineering is the process of discovering the technological principles of a device, object or system through analysis of its structure, function and operation. It often involves taking something apart and analyzing its workings in detail to be used in maintenance, or to try to make a new device or program that does the same thing without using or simply duplicating (without understanding) any part of the original. (Wikipedia)

TPS

TritonX-100-PAN-S :A self-synthesized water-soluble metal indicator with colorimetric selectivity for heavy metals.

Traffic light bioassay

Traffic light bioassay, the assay we have designed utilized similar indications as road signal for directing vehicular traffic by means of colored lights when we expect that several shades of blue imply different concentrations of heavy metal ions detected.