Cellulose is a polysaccharide made up of the monomer, B-D glucose, linked by (1->4) glycosidic bond [1]. It is an important structural component of the plant cell walls and has been used in various textile applications such as paper production [2]. Cellulose is also produced by a Gram-negative bacterium, Gluconacetobacter hansenii, which secretes highly-crystalline cellulose [3]. Because of the few requirements needed to produce bacterial cellulose, G. hansenii is seen as a model organism for the study of cellulose synthesis in plants [3]. We grew a large culture of G. hansenii in growth medium to produce large batch of bacterial cellulose. After retrieving the cellulose from the medium, we used a paper-making protocol to turn them into cellulose sheets (see protocol below). The cellulose would be an important substrate for our biOrigami when combined with the spores to make bioHYDRAS (link to bioHYDRA page). We can use CBDs to attach the spores to the cellulose sheet. This can be accomplished by using a DNA linker connecting the CBD sequence to a protein expressed on the spore coat, Cotz. Since Cotz localizes to the spore coat, the hybrid Cotz-CBD will allow the spores to attach to the sheet. Furthermore, we can expand on the unique properties of this CBD to allow attachment of any protein onto a cellulose surface. We call our CBD system uCBD to note its universal protein attachment abilities.

The system is inspired by the previous 2014 Stanford-Brown-Spelman iGEM team (link to page); however, it has several improvements. We used the cellulosomal-scaffolding protein A (cipA) of Clostridium thermocellum as our CBD. We chose cipA because of its high cellulose binding affinity (tested by the Imperial 2014 IGEM team); furthermore, we improved on the Imperial cipA by removing the illegal EcoRI site within the gene. CipA is attached to a monomeric streptavidin instead of the wild-type tetramer streptavidin to prevent the chance of protein aggregation, which can inhibit protein function [4]. We thus, sacrifice a small decrease in binding affinity from the monomeric streptavidin for an increase in functional activity of the overall hybrid protein. Together, the monomeric streptavidin and cipa (mSA-cipA) gene made up the cellulose attachment part of our uCBD sytem (Part I). The second part of the system involves molecular cloning any protein of interest onto the bifunctional ligase/repressor (birA) protein attached to an acceptor peptide. BirA is found in E. coli and it catalyzes attachment of biotin onto the biotin acceptor peptide such as the Avitag [5]. Because the acceptor peptide is connected to the protein of interest, this protein can be extracted and purified from the cells and can then attach to Part I via streptavidin-biotin interaction. The overall second construct would be called protein of interest-birA (POI-birA)

We made bacterial cellulose using G. hansenii and processed them into flat cellulose sheet. We also designed and cloned the mSA-cipA and POI-birA into NEB-5 alpha competent E. coli . Sequencing result agrees is consistent for mSA-cipA; however, our cloning for POI-birA was unsuccessful. This is because of a PstI site within the gene that causes difficulty in cloning. Further experiment will be done to resolve this problem.

Picture of cellulose before and after Sequencing Result for cipA.

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Protocols

Cellulose Sheets

Cellulose Production: We produced cellulose using Gluconobacter hansenii, the bacterium known to provide the highest cellulose yield (Ross et al, 1991). To produce cellulose from G. hansenii, we used the 2014 Stanford-Brown-Spelman iGEM team’s protocol, as below, with one slight modification – the addition of fructose to promote cellulose production (Embuscado, Marks & BeMiller, 1994).

Modified Acetobacter xylinum medium recipe (makes 500 mL media, see original source):

• 25g Fructose
• 10g Glucose
• 2.5g Tryptone (or peptone)
• 2.5g Yeast Extract
• 1.35g Na2HPO4
• 0.75g Citric Acid
• 500mL Water

Inoculate with G. hansenii culture and incubate at room temperature for up to one week or until desired volume is achieved.

Troubleshooting tips:

Contamination - When producing cellulose in large vats, contamination by fungi or bacteria can become a major issue.

Recommendations -

• Be certain to work with G. hansenii in the hood and to thoroughly seal the vats.
• You can also try adding an antifungal that will not act upon bacteria to the medium.
• The strain of G. hansenii we are using has some resistance to kanamycin, so you could perhaps try adding that. Wild-type bacteria sometimes have natural resistance to certain antibiotics, so we ran a quick experiment to see if G. hansenii is resistant to any of the antibiotics in our lab. There was some growth in the kanamycin plates / cultures – however, it was too slow to merit the addition of kanamycin to all cultures.
• You could also try transforming the G. hansenii via electroporation (see 2014’s adapted Acetobacter transformation protocol here).
• If all else fails, you could grow G. hansenii in a large (and we mean LARGE) Erlenmeyer flask. This significantly reduces risk of contamination, although surface area is limited.

No growth – The cellulose has stopped growing after a while.

Recommendation - If cellulose is no longer being produced, try adding extra glucose/fructose. Bacteria can’t make cellulose out of thin air!

Cellulose Processing: By solving key issues in cellulose processing, we hope to expand the possibilities of microbial cellulose. We identified brittleness to be the major problem, given that it results in poor flexibility (especially bad for folding) and limited strength of material. Additionally, we theorized that breaking down residual cell components could improve cellulose binding and sheet color. After an investigation spanning from literature reviews to DIY paper making forums, we decided to use glycerol to greatly enhance flexibility and integrity, as well as acetic acid to gently remove extraneous cell structures and pigments from the cellulose.

Here is the protocol we developed to process cellulose sheets:

1. Soak in acetic acid for one hour.
2. Wash with ddH2O a few times.
3. Soak in glycerol for one hour.
4. Separate layers for thinner sheets, if desired. (Applying friction to the sheets with a gloved hand should lead to separation of sheets from each other. If not, and thinner sheets are desired, cut down one end of the sheet and then pull apart.)
5. Soak in glycerol again briefly (~5 min).
6. Dry sheets on cardstock and paper towels. Place heavy object on top to flatten sheet and speed absorption.

Cellulose Binding Domains

Transformation: Chemically and electrocompetent NEB-5 alpha E. coli cells from New England Biolabs were used for all parts of this project. Protocols were followed according to the manufactur's instructions. Plates containing successful transformants were stored at 4C.

Growing Culture . Transformed cells were inoculated into 3 ml Lysogeny Broth (LB) medium supplemented with chloramphenicol and shaken at 37C for 24 hours. Growing culture for protein purification were inoculated in 100 ml LB medium instead.

Flag-tag Protein Purification:

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References

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