Team:Rotterdam HR/Notebook

Notebook

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Team page

May 10

Rens Boeser
Created the first prototype for the team page
01

Team page

May 10

Footer

May 20

Rens Boeser
Social media created
01

Footer

May 20

Footer

May 21

Rens Boeser
Social media buttons same color and fixed iGEM style issues
02

Footer

May 21

Notebook

May 24

Rens Boeser
Multiple week summary styles created for the notes
01

Notebook

May 24

Header

May 27

Rens Boeser
Added the header with mobile compatibility als resized logos and readded them to the header
01

Header

May 27

Main template

May 28

Rens Boeser
Added template header and footer with 'under construction' content
01

Main template

May 28

Header

May 28

Rens Boeser
Small fixes and menu adjustments
02

Header

May 28

Team

May 29

Rens Boeser
Added a PI list with the secondary PI
02

Team

May 29

Main page

June 7

Rens Boeser
Designed and added content holders to the index Page
01

Main page

June 7

Team

June 9

Rens Boeser
Added myself to the teammember Page and did some bugfixing
03

Team

June 9

Header

June 9

Rens Boeser
Started working on a better looking menubar
03

Header

June 9

Header

June 10

Rens Boeser
Added the ability to add sub-menus to items in the menu bar. Integration into the website and added indication for which Page you are on
04

Header

June 10

Construction pages

June 13

Rens Boeser
Updated all Pages to the new style with an under construction sign
01

Construction pages

June 13

Header

June 14

Rens Boeser
Added a way to recognise Pages under construction using the menubar
05

Header

June 14

Main page

June 14

Rens Boeser
Updated the content containers so that they are responsive
02

Main page

June 14

Architecture design [TC]

June 18

Tom van Dijk | Mike Vrieswijk
The first draft of the architecture design for the temperature controller was made.
01

Architecture design [TC]

June 18

Human Practices page

June 22

Rens Boeser
Content added to the human practices page
01

Human Practices page

June 22

Main page

June 23

Rens Boeser
Content created and added to the main page
03

Main page

June 23

Architecture design [TC]

June 24

Tom van Dijk | Mike Vrieswijk
Today a few changes have been made to the architecture design of the temperature controller. The choice was made to use a premade power supply as opposed to a self-made one, because this was considering the time left to finish this device the best choice. A few alterations were made to make the architecture design better readable.
02

Architecture design [TC]

June 24

First prototype [TC]

June 25

Tom van Dijk | Mike Vrieswijk
A 3d drawing was made for the casing that will hold the temperature controller. The first prototype was printed, but was determent to be inadequate due to the lack of enough space for the cooler block.
01

First prototype [TC]

June 25

Team

June 26

Rens Boeser
Added the remaining instructors to the team
04

Team

June 26

Second prototype [TC]

June 26

Tom van Dijk | Mike Vrieswijk
In the drawing space was added to fit the cooler block for the temperature controller. Slits were added to the drawing for the nuts to slide into. The altered drawing was printed. The newly printed parts, cooler block, fan and Peltier element were assembled. Everything fit together.
02

Second prototype [TC]

June 26

Testrun [TC]

June 27

Tom van Dijk | Mike Vrieswijk
A short test run was done with the newly assembled cooler. The test concluded that the temperature controller could cool a water droplet to the point of freezing and heat it back up to its boiling point.
03

Testrun [TC]

June 27

Draft decision

July 2

Tom van Dijk | Mike Vrieswijk
The choice to use a computer PSU as a power supply was made. The choice was made on the grounds, that computer PSU have a standard 12, 5 and 3.3V output. This is beneficial because these are the voltages necessary for the selected components.
01

Draft decision

July 2

Architecture design [TC]

July 5

Tom van Dijk | Mike Vrieswijk
Changes were made to the architecture design of the temperature controller. Different voltage regulators were selected to fit the newly chosen power supply. To better readability of the architecture design a legend was added.
03

Architecture design [TC]

July 5

Electrical circuit design [TC]

July 8

Tom van Dijk | Mike Vrieswijk
Custom footprints were made for multiple components and added to the parts library in the PCB design software.
01

Electrical circuit design [TC]

July 8

Electrical circuit design [TC]

July 9

Tom van Dijk | Mike Vrieswijk
The provisional electronic circuit design for the temperature controller was made.
02

Electrical circuit design [TC]

July 9

Electrical circuit design [TC]

July 11

Tom van Dijk | Mike Vrieswijk
The electronic circuit design for the temperature controller was finished. Measuring point were added to the electronic circuit design.
03

Electrical circuit design [TC]

July 11

Stock up

July 11

Elise Grootscholten | Loraine Nelson | Paul Reusink
To have some basic biobricks ready, we stocked them by doing a plasmid isolation and freeze the DNA.
01

Stock up

July 11

Basic parts

July 11

Elise Grootscholten | Loraine Nelson | Paul Reusink
To start on a basic construct we did a digestion and ligation with the parts we isolated earlier. To prevent original constructs we did a defosphorylation after the digestion. We controlled the digestion by doing a gelelktroforeses.
01

Basic parts

July 11

Board layout [TC]

July 12

Tom van Dijk | Mike Vrieswijk
Started working on the board layout for the PCB of the temperature controller.
01

Board layout [TC]

July 12

Basic parts

July 12

Tom van Dijk | Randall de Waard
We continued with the ligated DNA by transformating it to Neb10Beta. This was plated onto agarplates and incubated for 1 day.
02

Basic parts

July 12

Board layout [TC]

July 13

Tom van Dijk | Mike Vrieswijk
Further work was done to the board layout for the temperature controller.
02

Board layout [TC]

July 13

Basic parts

July 13

Elise Grootscholten | Randall de Waard
The results of 7/12/2018 were collected, in action of this we decided to plate some ligated and transferred DNA from 7/12/2018 again. This we did because there wasn't a clear grow of colonies on the plates.
03

Basic parts

July 13

Blue White screening on paper

July 13

Elise Grootscholten | Randall de Waard
We tried to let bacteria grow on paper, therefore we used our own buisnesscards. We let the buisnesscards absorb some LB-medium and put them inside petridishes.
01

Blue White screening on paper

July 13

Board layout [TC]

July 15

Tom van Dijk | Mike Vrieswijk
Work has been done on the board layout for the temperature controller. The board layout is now finished.
03

Board layout [TC]

July 15

Basic parts

July 16

Mei Ju Goemans | Elise Grootscholten | Dustin van der Meulen | Randall de Waard
To know if the ligation was succesfull we will controll the DNA, therefor we ented the bacteria's with DNA in LB-medium to grow overnight. We also plated the used bacteria's onto new plates to use for further experiments.
04

Basic parts

July 16

Blue White screening on paper

July 16

Mei Ju Goemans | Elise Grootscholten | Dustin van der Meulen | Randall de Waard
We did a blue white screening on our buisnesscards to see if bacteria had grew on them. We transferred the buisnesscards to new petrydishes and added ITPG and X-gal to the petrydishes.
02

Blue White screening on paper

July 16

Notebook

July 17

Rens Boeser
Frontend design for the notebook
02

Notebook

July 17

Basic parts

July 17

Rens Boeser | Dustin van der Meulen | Loraine Nelson | Suzanne Romeijn | Randall de Waard
The resulst of 7/16/2018 showed that the DNA didnt ligate as planned. To be able to digest enough DNA we did a plasmid isolation again. We digested this DNA and froze it for further use.
05

Basic parts

July 17

Stock up

July 18

Dustin van der Meulen | Loraine Nelson | Suzanne Romeijn | Mike Vrieswijk | Randall de Waard
We did another round of plasmid isolation for stocking.
02

Stock up

July 18

Notebook

July 19

Rens Boeser
Designed a way to follow experiments that take up multiple days and eventually designed a notebook entry page and made it a responsive page
03

Notebook

July 19

Basic parts

July 19

Dustin van der Meulen | Mei Ju Goemans| Randall de Waard
We digested all DNA we have in stock to test for our basic construct. We tested the DNA by doing a gelelktroforeses.
06

Basic parts

July 19

Notebook

July 21

Rens Boeser
Created a one page notebook. Made the notebook entry page more suited for the entry length
04

Notebook

July 21

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

July 23

UNKNOWN

Transformations of the biobricks K133071, K173003 and I13453 are performed. K133071 will produce CO2 if there's pyruvate present and K173003 will produce CO2 if urea is present. I13453 is a promotor which will work if there's arabinose present.                                                                                                        
The biobricks were transformed first into electrocometent cells and later into chemical competent cells from the strain NEb10Beta. After transformations the culture was plated on agar plates with antibiotics. The first transformations didn't work out, but the second did, because then the right competent cells were used. 

1

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

July 23

ATP sensor

July 24

Rens Boeser | Mei Ju Goemans | Elise Grootscholten | Dustin van der Meulen | Loraine Nelson | Suzanne Romeijn | Randall de Waard
New biobricks, used to make an ATP sensor, were transformed into NEB10Beta. The culture was than plated onto agar and incubated for 1 day.
01

ATP sensor

July 24

Gas output

July 24

Rens Boeser | Mei Ju Goemans | Elise Grootscholten | Dustin van der Meulen | Loraine Nelson | Suzanne Romeijn | Randall de Waard
New biobricks, which produces gasses, were transformed into NEB10Beta. The culture was than plated onto agar and incubated for 1 day.
01

Gas output

July 24

Notebook generator

July 24

Rens Boeser
Started working on an automatic notebook creator
01

Notebook generator

July 24

Transformation

July 24

UNKNOWN

Today we did a transformation with new biobricks. The biobricks were built into chemically competent cells from the strain NEb10Beta. After transformation the culture was plated on agar plates with antibiotics. The results were checked the next day. 

1

Transformation

July 24

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

July 24

UNKNOWN

To be able to always get the necessary biobricks, there have been made glycerolstocks of the transformed biobricks K133071, K173003 and I13453. The glycerolstocks are stored at -80 degrees Celsius. If needed, they can be retrieved from this storage to use for experiments. 

2

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

July 24

Notebook generator

July 25

Rens Boeser
Automatic generation of entries completed
02

Notebook generator

July 25

Google Drive API

July 25

Rens Boeser
Used the Google drive REST API to download the entries from drive
01

Google Drive API

July 25

Automatic uploader

July 25

Rens Boeser
Used the igemwiki API to update pages using software
01

Automatic uploader

July 25

Transformation

July 27

UNKNOWN

To be able to always get the necessary biobricks, we made an glycerol stock after every transformation. The glycerol stocks are stored at -80 degrees Celsius. If needed, they can retrieved from this storage to use for experiments. 

2

Transformation

July 27

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

July 27

UNKNOWN

For further experiments there is isolated DNA needed of the biobricks J23100, K133071, K173003 and I134353. The DNA is isolated out of the bacteria with the help of a plasmid purifaction kit. After isolation this DNA can be used for digestion and ligation or other experiments. J23100 (from the glycerolstock): 325,59 ng/ul, K173003: 217,06 ng/ul, K133071: 186,79 ng/ul, I13453: 88,18 ng/ul

3

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

July 27

Automation program

July 29

Rens Boeser
Connected the page uploader to the notebook generator
01

Automation program

July 29

Automatic uploader

July 29

Rens Boeser
Created a program that uploads all updated pages
02

Automatic uploader

July 29

Page generator

July 31

Rens Boeser
Built a page builder that automatically adds the header and footer before uploading
01

Page generator

July 31

Google Drive API

July 31

Rens Boeser
Redone the google API handler for reusability and readability and made the google API handler generic
02

Google Drive API

July 31

Automation program

July 31

Rens Boeser
revamped the main program
02

Automation program

July 31

Automation program

August 1

Rens Boeser
Finished redoing the application for generating and uploading pages
03

Automation program

August 1

Notebook

August 2

Rens Boeser
Added month categorization to the page
05

Notebook

August 2

Transformation

August 9

UNKNOWN

For further experiments we needed isolated DNA. The DNA is isolated out of the bacteria with the help of a plasmid purifaction kit. After isolation this DNA can be used for digestion and ligation or other experiments.

3

Transformation

August 9

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

August 10

UNKNOWN

The biobricks J23100, K133071, K173003 and I134353 were sucessfully digested after the second time. After the digestions the biobricks K133071 and K173003 were dephosphorylated and ligated with the inserts J23100 and I13453. This was done in the original backbone of K133071 and K173003, and not another control backbone. To know if the biobricks were right ligated this was done by testing practically. See the experiments: Testing gas production. 

4

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

August 10

Urea and sodium pyruvate test for resistence E.coli

August 10

UNKNOWN

Testing different amounts of urea and sodiumpyruvate to know which concentrations the bacteria survive.

1

Urea and sodium pyruvate test for resistence E.coli

August 10

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

August 13

UNKNOWN

Transformations of the biobricks (K133071 + J23100), (K13071 + I1345), (K173003 + J23100) and (K173003 + I13453) in NEB10B�ta. There was no grow except for the biobrick combination K133071 + J23100.

5

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

August 13

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

August 13

UNKNOWN

A colony PCR is done for the NEB10B�ta E.coli cells with expected the biobrick combination of K133071 with J23100. Nevertheless, on a gel the difference with and without promotor couldn't be seen. So there must be another way of proving the right biobricks are there.

6

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

August 13

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

August 13

UNKNOWN
The ligations and transformations of the biobricks K173003 + J23100, K173003 + I13453, and K133071 + I13453 has been performed again. There was a lot of grow on the agar plates. To know if the biobricks were right ligated this was done by testing practically. See the experiments: Testing gas production. 
7

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

August 13

Testing gas production

August 16

UNKNOWN

Making a set up for the gas production testing and testing it with NEB10B�ta with the expected biobricks in it (K133071 + J23100) and a negative control.

1

Testing gas production

August 16

Testing gas production

August 23

UNKNOWN

Making a set up for the gas production testing and testing it with NEB10B�ta with the expected biobricks in it (K133071 + I13453), (K173003 + J23100), (K173003 + I13453) and a negative control.

2

Testing gas production

August 23

Testing gas production

August 23

UNKNOWN

Gasproduction testing for the biobricks (K173003 + I13453), (K133071 + I13453) and negative controls (B0015 and K133071 without urea and arabinose).
K173003 + I13453 is tested with sodiumpyruvate and arabinose for gasproduction and K133071 + I13453 is tested with urea and arabinose for gasproduction.

3

Testing gas production

August 23

Testing gas production

August 23

UNKNOWN

Testing the gasproduction of the colonies 9 and 10 of biobricks (K173003 + J23100), colonies 5 and 7 of biobricks (K173003 + I13453) and colony 4 of biobricks (K133071 + I13453) with and without centrifuging the bacteria. There is also a negative control (J04450 pSB1K3) with Kanamycine. 

4

Testing gas production

August 23

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

August 27

UNKNOWN

Minipreps are made of colonies 11 and 19 of biobrick combination K133071 + J23100. Results: 11. 270,57 ng/ul 19. 253,59 ng/ul.

8

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

August 27

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

August 27

UNKNOWN

A miniprep of the biobrick K352002 is made. The concentration is 69,77 ng/ul.

9

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

August 27

Urea and sodium pyruvate test for resistence E.coli

August 28

UNKNOWN

Testing different amounts of urea and sodiumpyruvate to know which concentrations the bacteria survive.

2

Urea and sodium pyruvate test for resistence E.coli

August 28

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

September 7

UNKNOWN

Digestions, gelelectrophoresis, dephosphorylations and ligations of different biobrick combinations. These biobrick combinations are 4 different promotors (J23100, I13453, K352002, K352003)  with 4 different gasproduction biobricks (k173003, K173013, K133071, K133116). J23100 is about 1 kb to long. The rest seems likely to be right digested. The ligations will be transformed in NEB10b�ta and digested again as control.

10

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

September 7

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

September 7

UNKNOWN

Transformations of the biobrick combinations in NEB10b�ta. The transformations are plated on kanamycine agar plates, because all the ligations were done in pSB1K3 (kanamycine resistence) backbone. Pink and with colonies appeared after incubation by 37 degrees Celcius for about 12h. The white colonies will be used for further experiments.

11

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

September 7

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

September 11

UNKNOWN

Plasmid DNA was isolated of 20 different colonies. The first time something went wrong. The second time we had good concentrations of isolated plasmid DNA. After this we will digest the DNA to see if the plasmids all have the required biobricks.

12

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

September 11

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

September 11

UNKNOWN

The minipreps of experiment 12 are digested with the restriction enzymes: SmaI and ScaI.

13

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

September 11

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

September 17

UNKNOWN

Minipreps of the biobrick combinations: K352002+K133116+pSB1K3 (1) and K352003+K133116+pSB1K3 (2) are done. The DNA concentration is for 1:189,3 ng/�l and for 2: 355,3 ng/�l.

14

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

September 17

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

September 17

UNKNOWN

15

Cloning Multiple BioBricks to Assess Gas Production BioBricks in E.Coli

September 17

Testing gas production

September 17

UNKNOWN

Different species/tribes? of E.coli are tested as negative control. Those spacies/tribes? were: NEB10B�ta, BL21 (DE3), BL21, HB101, DH5alpha and JM109. NEB10B�ta produced the most gas. BL21, HB101 and JM101 produced none/almost none gas. Because BL21 isn't a K12 tribe? we can not use that one. That is why we will test further gasproduction in HB101 and JM109. And maybe those will be our final E.coli tribes.

5

Testing gas production

September 17