Hardware

Our Arduino starter kits arrived! Make an LED blink. that’s how it begins.

Molecular Toolbox

CRISPR-Cas9 induced PEX10knockout

Y. lipolytica PO1f genome sequence was annotated and protospacer for targeting PEX10 was designed and ordered from IDT. Protospacer for Gibson Assembly with CRISPRyl plasmid (Addgene plasmid #70007) SCR1'- tRNAGly (bold), Protospacer (underlined), sgRNA (italic) 5'-GGGTCGGCGCAGGTTGACGTGTACAAGGAGGAGCTGGAGAGTTTTAGAGCTAGAAATAGC-3' Oligos designed to amplify a 1kb region upstream and downstream PEX10 and anneal together by fusion PCR were also ordered from IDT.

CRISPR-Cas9 induced URA3insertion

The Y. lipolytica PO1f genome sequence was annotated and uploaded to Benchling for sgRNA design. sgRNAs targeting the SUC2 gene were designed. Primers were designed that amplify the functional URA3 gene including 1 kb upstream and downstream flanking regions.

pSB1A8YL

Ran a bunch of PCRs to amplify the pUC19 part of our plasmid, but it’s not working - nothing but smear. Tried to transform the pUC19 plasmid into Escherichia coli.

Substrates

We did an initial experiment determining the full growth cycle of Y. lipolytica W29. This will be used to plan and time the following growth experiments. Waste glycerol from the industrial biodiesel producer DAKA is acquired for late screening.

Hardware

We started building light sensors using photoresistors. Shortlisting ideas for our final project: - A microtiter plate reader - Hack a printer to build a membrane homogenizer - Chemostat bioreactor

Molecular Toolbox

CRISPR-Cas9 induced PEX10knockout

Genomic DNA from Y. lipolytica PO1f Δku70 and Y. lipolytica W29 was purified. PEX10 flanking regions were successfully amplified from Y. lipolytica PO1f Δku70.

CRISPR-Cas9 induced URA3insertion

Genomic DNA from Y. lipolytica PO1f Δku70 and Y. lipolytica W29 was purified. - PCR attempts to amplify URA3 and flanks failed. - sgRNAs targeting the SUC2 gene were hybridized.

pSB1A8YL

Purified the plasmid from the transformants and use this as template for PCR, although it’s still not giving any bands.

Substrates

We did initial growth experiments on minimal media with an array of different carbon sources. This experiment was discarded due to lack of repeats and wrong vitamin solution for minimal media. Waste from canola oil production by Grønninggaard is acquired. Molasses from Dansukker sugar production is acquired.

Hardware

Exploring the Arduino IDE and all the electronic components we ordered. There is so much to learn.

Molecular Toolbox

CRISPR-Cas9 induced URA3insertion

PCR attempts to amplify URA3 + flanks from Y. lipolytica W29 genomic DNA failed. New primers were ordered.

pSB1A8YL

We realized that the name of the primer had been mixed up! Now that the right primers are used, we get excellent bands on our gel… Guess you have to make the stupid mistakes in the beginning? The gBlock containing the other part of the plasmid also arrived. This also gives excellent bands on the gel when amplifying it by PCR. Ran the first USER and transformed E. coli cells. The transformants were left on the bench over the weekend

Substrates

We have data from the first successful growth experiment. Starch, Xylose, Arabinose, Maltose and Lactose are not suitable for Y. lipolytica fermentation. This will be repeated next week to make sure. Waste glycerol from the industrial biodiesel producer Perstop is acquired.

Molecular Toolbox

CRISPR-Cas9 induced PEX10knockout

Received CRISPRyl plasmid (Addgene plasmid #70007). The procedure from Addgene was followed.

CRISPR-Cas9 induced URA3insertion

Successful amplification of URA3 + flanks from Y. lipolytica W29 genomic DNA. Because of low quality of the genomic DNA, the initial PCR product was taken for further amplification. Received CRISPRyl plasmid (Addgene plasmid #70007). The procedure from Addgene was followed.

pSB1A8YL

YES, colonies! colonies were picked and used for colony PCR, but it was not successful. We’ll just have to crank on! - Colonies from the same plates were re streaked and plasmids were purified from the resulting colonies. - Restriction analysis yielded weird bands. - This week passes restreaking colonies to yield pure colonies and trying to find the correct transformants through by purifying the plasmids and subjecting it to analytical digestion. So far no luck!

Substrates

Repeated positive results with growth on glucose, glycerol, fructose, sucrose and oil. Y. lipolytica should not be able to grow on sucrose. The experiments on starch, xylose, arabinose, Maltose and Lactose are still negative for Y. lipolytica. Waste glycerol from the industrial biodiesel producer Emmelev is acquired.

Genome Scale Modeling

Planning of Genome-scale modelling strategies began, decided to attempt media optimization using phenotype phase plane, team starts to research and learn FBA for GSM.

Software

Initiation of task by designing the workflow needed to achieve the final purpose of the software. Tasks agreed upon discussion : script in python , number and format proxy of the input files needed , restriction site implementation , development GUI, gui library for python (tkinter)

Hardware

Still playing.

Molecular Toolbox

CRISPR-Cas9 induced PEX10knockout

The assembled CRISPRyl plasmid with PEX10 protospacers was transformed in competent E. coli DH5α cells. Purification of assembled CRISPRyl plasmid with Pex10 protospacers. The assembled CRISPRyl plasmid with PEX10 protospacers was digested with AvrII to test if the PEX10 protospacer was inserted. The digestion was successful and showed no cutting by AvrII indicating correct insertion of PEX10 protospacers. First attempt of transformation with CRISPRyl plasmid with PEX10 protospacers in Yarowia lipolytica PO1f Δku70. The transformation was unsuccessful. There was growth all over the plates.

CRISPR-Cas9 induced URA3insertion

Confirmation of successful Gibson assembly through restriction analysis. First (unsuccessful) transformation of pCRISPRyl and pCRISPRyl+sgRNAs into Yarowia lipolytica PO1f Δku70.

Products

Beta-Carotene

BioBricks BBa_K152005 (crtE,crtI,crtYB,gfp) and BBa_K530002 (crtI) were received from the registry. E. coli with BBa_K152005 could only grow without Ampicilin, so we suspect a problem with the AmpR backbone. We decided not to use this biobrick and instead only work with BBa_K530002, BBa_K530000 and BBa_K530001.

Proinsulin

Designing and ordering synthetic gBlock from IDT encoding TEF1, proinsulin and GFP.

Substrates

Test shows no growth on samples of wastewater from areas contaminated with leftovers of organic molecules from fossil oil. Experiments with glycerol byproduct from Emmelev biodiesel production showed to be contaminated. We investigated where the contaminations could come from and a contaminated pipet seemed to be the source.

Hardware

The library for our LCD Display is commented in Chinese. Shoutout to James for translating. Chris, our supervisor, brought us in contact with Martin and Erik, two professors from DTU Nano and Elektro. Our university is running a new project course in January where 1st semester students ferment their own cultures and build devices to monitor growth. They built a measuring chamber and a simple circuit, reading the voltage over the photodiode with a multimeter. Isn’t there a way to do all this using an Arduino? We set a meeting for next week. Reading about digital to analog conversion(DAC) and the reverse(ADC). Dimming LEDs in the office

Molecular Toolbox

CRISPR-Cas9 induced PEX10knockout

Transformation in Y. lipolytica was repeated using the same transformation protocol from last week. However, this time less cells were used for the transformation. This did not work.

CRISPR-Cas9 induced URA3insertion

Gibson assembly of sgRNAs targeting SUC2 into pCRISPRyl. More (unsuccessful) transformations of pCRISPRyl and pCRISPRyl+sgRNAs into Yarowia lipolytica PO1f Δku70.

pSB1A8YL

The promoter was paired with the chromoproteins using 3A assembly. Unfortunately, no color was observed even though PCR and analytical digestion showed that the length of the construct are correct.

Promoters

TEF1 was amplified from gBlock by PCR. SCR1’-tRNA promoter was amplified from the pCRISPRyl plasmid by PCR with primers introducing a base substitution to remove illegal restriction site.

Products

Beta-Carotene

Biobricks BBa_K530000 (crtYB) and BBa_K530001 (crtE) from the distribution kit was successfully obtained. We designed Gibson primers including 5'-CACA-3' upstream of each start codon for assembly of all three genes.

Proinsulin

3A assembly of the proinsulin gBlock and pSB1C3. Electrophoresis did not confirm presence of desire plasmid.

Substrates

S. cerevisiae does not grow as well as Y. lipolytica on glycerol based waste, but has an advantage on sucrose based ones.

Genome Scale Modeling

Ben has kickstarted the modeling, by introducing the phenotype phase plane concept to the team, which is an extension to flux-balance analysis. The hope is that it will be possible to find optimal in-flow of various substrates in order to maximize product, in this case beta-carotene. Downloaded first Y. lipolytica model “MODEL1510060001”. Tutorials are studied in Matlab.

Software

Script writing is finished. Testing of functionality was initiated in order to find the most “sustainable” solution in terms of resources and the optimization step (reverse-translation) from the desired sequences to protein sequences. Approach decided for main body of script is building and checking the sequences “on the fly” while using as initial files the y_lip.txt (gcn), desired.fsa(protein sequences), ressites.txt(restriction sites).

Hardware

Successful tests at DTU Nano. We can measure growth of S. cerevisiae. Erik found a great photodetector that includes an amplifying circuit.

Molecular Toolbox

CRISPR-Cas9 induced PEX10knockout

Transformation in Y. lipolytica was repeated using transformation protocol from Cory M. Schwartz . The transformation was unsuccessful.

CRISPR-Cas9 induced URA3insertion

More (unsuccessful) transformations of pCRISPRyl and pCRISPRyl+sgRNAs into Yarowia lipolytica PO1f Δku70.

pSB1A8YL

Still trying to figure out why we do not see any color output... K592010 was retrieved from the distribution kit.

Promoters

3A assembly with the TEF1 fragment and pSB1C3 backbone. Results were inconclusive, so they were repeated in week 10.

Products

Beta-Carotene

PCR with Gibson primers on all three biobricks and pSB1C3 backbone. Only BBa_K53000 (crtYB) and backbone was successful. crtI and crtE was after several attemps successfully amplified with prefix10 and suffix10 primers, which then worked at template for PCR with Gibson primers.

Proinsulin

3A assembly was repeated. Once again desire plasmid was not obtained (confirmed with electrophoresis and restriction analysis). Gibson assembly of proinsulin gBlock and backbone pSB1C3. Transformation gave numerous colonies that were used as a template for colony PCR. One colony was expected to carry a desired construct, however further investigation disproved it.

Substrates

The Y. lipolytica growth on sucrose was found to be a false positive. The autoclavaton of sucrose breaks the molecule turning it into glucose and fructose. S. cerevisiae grow faster do to the ability to metabolize sucrose, while Y. lipolytica can only utilize the glucose and fructose.

Hardware

Running more fermentations together with Martin and Erik. They changed their design while we got inspired for our final project. Couldn’t we turn this into a cheap alternative for the Hamilton robot? Reading on CAD drawings, 3D printing and laser cutting