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Contents 1 Bacterial specific methods 1.1 Generating electrocompetent cells 1.2 Transformation via electroporation 1.3 Transformation of Single Step (KRX) Competent Cells by Promega 1.4 Standard BioBrick Assembly 1.4.1 Suffix Insertion 1.4.2 Prefix Insertion 1.4.3 Variations 1.5 Standard Freiburg BioBrick Assembly 1.5.1 Suffix Insertion 1.5.2 Prefix Insertion 1.5.3 Variations 1.5.4 Restriction analysis 1.6 Colony PCR 2 Plants specific methods 2.1 Arabidopsis thaliana: Growth Conditions and Plant Material 2.2 Arabidopsis thaliana: Total RNA Isolation 2.3 Arabidopsis thaliana: cDNA Synthesis 2.4 PCR for A.thaliana laccase ampflification 3 Yeast specific methods 3.1 Genomic DNA isolation 3.2 Generating electrocompetent cells 4 General methods 4.1 Ethanol precipitation to clean DNA

Bacterial specific methods

Generating electrocompetent cells

(E.coli-[http://www.promega.com/products/cloning-and-dna-markers/cloning-tools-and-competent-cells/bacterial-strains-and-competent-cells/single-step-_krx_-competent-cells/ KRX], [http://www.genomics.agilent.com/files/Manual/200249.pdf XLI Blue] and [http://www.merckmillipore.com/is-bin/INTERSHOP.enfinity/WFS/Merck-DE-Site/de_DE/-/EUR/ViewPDF-Print.pdf;sid=MURSuevozHZ2ubuzCYY-7kMotsdASYFPCWpM71hFGa-SnWVmHaQxE-3WJh_fBJar5MJCpegxzHx7vmIhk8DOvz7AELBL_Sc4At7qmFPx-WwuKfv0Mp2vgcLv?RenderPageType=ProductDetail&CatalogCategoryID=&ProductUUID=6t.b.s1OalsAAAEY0BwK0D3I&PortalCatalogUUID=tUmb.s1O2d0AAAEXcutI1u8e Rosetta gami] )

Materials:

• 550 mL LB-Medium
• 1 L cooled bidest. H₂O
• 150 mL cooled 10 % glycerine
• 10 pre-cooled 50 mL Falcons (-18°C)

Protocol:

• Inoculate 2x3 mL LB with bacterial stock; incubate over night at 37 °C and 140 rpm
• Inoculate 2x250 mL LB with the over night cultures in 1-litre-flask (with baffles) at 37 °C and 140 rpm
• Incubate until OD₆₀₀ 0,4-0,6
• Cool the culture 15-30 minutes on ice

Important: keep your cells at 2-4 °C during the following steps

• Divide the cultures into cooled 50 mL Falcons and centrifugate for 15 minutes (4000 rpm, 4 °C) IMPORTANT: slowly accelerate and deccelerate
• Discard supernatant
• Resuspend cell pellet in 5 mL cooled bidest H₂O (and don't get frustrated while doing it, keep shaking gently)
• Pool two suspensions each, add bidest H₂O up to 50 mL and centrifugate again (see centrifugation above)
• Discard supernatant (Keep in mind: keep your cells at 2-4 °C)
• Resuspend pellet in 5 mL cooled bidest H₂O
• Add bidest H₂O up to 50 mL and centrifugate again (see centrifugation above)
• Discard supernatant (Keep in mind: keep your cells at 2-4 °C)
• Resuspend pellet in 5 mL cooled 10 % glycerine
• Transfer suspensions in two 50 mL Falcons and centrifugate again (see centrifugation above)
• Discard supernatant
• Add volume of 10 % cooled glycerine (2-4°C) that is approximately equal to the volume of the pellet and resuspend
• Divide cells in 100 μL aliquots and freeze in liquid N₂ immediately
• Store at -80 °C

Transformation via electroporation

• Thaw 50 µL competent E.coli cells on ice, dilute with icecold 50 µL glycerine (10 %) if necessary
• Add 0.5-2 µL plasmid to 50 µl electrocompetent cells
• Store cells on ice for 1 minute
• Electroporate at U = 2.5 kV, C = 25 µF, R = 400 Ώ
• Transfer transformation reaction to 450 µL SOC-Medium and shake 1 h at 37 °C
• Centrifuge 2 min at 800 rpm and plate on selective LB-Medium

Transformation of Single Step (KRX) Competent Cells by Promega

Using [http://www.promega.com/~/media/Files/Resources/Protocols/Technical%20Bulletins/101/Single%20Step%20Competent%20Cells%20Protocol.ashx protocol E. coli KRX single step competent cells by Promega]

• Remove Single Step (KRX) Competent Cells from –70 °C, and place on ice for 5 minutes or until just thawed.
• Add 1–50 ng of DNA (in a volume not greater than 5 μL) to the Single Step (KRX) Competent Cells. Move the pipette tip through the cells while dispensing. Quickly flick the tube several times. Do not vortex!
• Immediately return the tubes to ice for 5–30 minutes
• Heat-shock cells for 15–20 seconds in a water bath at exactly 42 °C. Do not shake.
• Immediately place the tubes on ice for 2 minutes.
• Add 450 μL of room-temperature SOC-Medium to each transformation reaction, and incubate for 60 minutes at 37 °C with shaking (approximately 225 rpm). For best transformation efficiency, lay the tubes on their sides and tape them to the platform.
• For each transformation reaction, we recommend plating 100 μL of undiluted cells and 1:10 and 1:100 cell dilutions on antibiotic plates. Incubate the plates at 37 °C over night.

Standard BioBrick Assembly

modified from [http://openwetware.org/wiki/Silver:_BB_Strategy Silver lab]: This assembly method can be used for BioBricks which are bigger than 150 bp. The BioBrick should be at least 500 bp bigger or smaller than the backbone. The BioBrick, which complies with these conditions, is used as the insert and is assembled into the prefix or suffix of the other used BioBrick, called vector. So you have to differentiate between a prefix and a suffix insertion.

Suffix Insertion

• Digestion of insert: at least 700 ng DNA / 10 µL volume, 1 µL 10x Tango buffer, 0.5 µL XbaI, 1 µL PstI. Digest for 2 h to 4 h at 37 °C, afterwards inactivation for 20 min at 80 °C. Clean up the insert via gel electrophoresis. When cutting the insert out of the gel try to avoid staining or exposure to ultraviolet light of the insert.
• Digestion of vector about 700 ng DNA / 10 µL volume, 1 µL 10x orange buffer, 0.5 µL SpeI, 0.5 µL PstI. Digest for 2 h to 4 h at 37 °C, afterwards inactivation for 20 min at 80 °C. Add 1 µL SAP (shrimp alcaline phosphatase) and 1.2 µL 10 x SAP buffer, incubate for 1 h at 37 °C. Clean up the vector via gel electrophoresis and PCR clean-up kit.
• Ligation: after digestion and clean-up: 50 - 100 ng of vector, 3 - 10 fold molar access of insert, 20 µL ligation volume, 2 µL T4-Ligase-Buffer, 1 µL T4-Ligase. Incubate for 20 - 30 min at room temperature, afterwards inactivation for 5 min at 70 °C. Then: store at -20 °C or transform.

Prefix Insertion

• Digestion of insert: at least 700 ng DNA / 10 µL volume, 1 µL 10x BamHI buffer, 0.5 µL EcoRI, 0.5 µL SpeI. Digest for 2 h at 37 °C, afterwards inactivation for 20 min at 80 °C. Clean up the insert via gel electrophoresis. When cutting the insert out of the gel try to avoid staining or exposure to ultraviolet light of the insert.
• Digestion of vector about 700 ng DNA / 10 µL volume, 1 µL 10 x Tango buffer, 0.5 µL EcoRI, 0.5 µL XbaI. Digest for 2h at 37 °C, afterwards inactivation for 20 min at 80 °C. Add 1 µL SAP (shrimp alkaline phosphatase) and 1.2 µL 10 x SAP buffer, incubate for 1 h at 37 °C. Clean up the vector via gel electrophoresis and PCR clean-up kit.
• Ligation: after digestion and clean-up: 50 - 100 ng of vector, 3 - 10 fold molar access of insert, 20 µL ligation volume, 2 µL T4-Ligase-Buffer, 1 µL T4-Ligase. Incubate for 20 - 30 min at room temperature, afterwards inactivation for 5 min at 70 °C. Then: store at -20 °C or transform.

Variations

• A digestion over night is possible. If you digest over night use only 0.1 µL restriction enzyme.
• It is also possible to use PCR product as insert. Digest after PCR with corresponding restriction enzymes and clean up with PCR clean-up kit. This could lead to higher yields of insert DNA because a lot of DNA gets lost during the gel electrophoresis clean up.

Standard Freiburg BioBrick Assembly

Modified from [http://openwetware.org/wiki/Silver:_BB_Strategy Silver lab] and [http://partsregistry.org/Assembly_standard_25 Assembly standard 25]:

This assembly method can be used for fusion protein assemblies with BioBricks which are bigger than 150 bp. The BioBrick should be at least 500 bp bigger or smaller than the backbone. The BioBrick, which complies with these conditions, is used as the insert and is assembled into the prefix or suffix of the other used BioBrick, which is called vector and needs to be available in the BioBrick [http://partsregistry.org/Assembly_standard_25 Assembly standard 25]. You have to differentiate between a prefix and a suffix insertion.

Suffix Insertion

• Digestion of insert: at least 700 ng DNA / 10 µL volume, 1 µL 10x NEB buffer 4 + 0.1 µL 100x BSA, 0.5 µL NgoMIV (NEB), 1 µL PstI. Digest for 2 h at 37 °C, afterwards inactivation for 20 min at 80 °C. Clean up the insert via gel electrophoresis. When cutting the insert out of the gel try to avoid staining or exposure to ultraviolet light of the insert.
• Digestion of vector about 700 ng DNA / 10 µL volume, 1 µL 10x orange buffer, 0.5 µL AgeI, 0.5 µL PstI. Digest for 2 h at 37 °C, afterwards inactivation for 20 min at 80 °C. Add 1 µL SAP (shrimp alkaline phosphatase) and 1.2 µL 10x SAP buffer, incubate for 1 h at 37 °C. Clean up the vector via gel electrophoresis and PCR clean-up kit.
• Ligation: after digestion and clean-up: 50 - 100 ng of vector, 3 - 10 fold molar access of insert, 20 µL ligation volume, 2 µL T4-Ligase-Buffer, 1 µL T4-Ligase. Incubate for 20 - 30 min at room temperature, afterwards inactivation for 5 min at 70 °C. Then: store at -20 °C or transform.

Prefix Insertion

• Digestion of insert: at least 700 ng DNA / 10 µL volume, 1 µL 10x orange buffer, 0.5 µL EcoRI, 0.5 µL AgeI. Digest for 2 h to 4 h at 37 °C, afterwards inactivation for 20 min at 80 °C. Clean up the insert via gel electrophoresis. When cutting the insert out of the gel try to avoid staining or exposure to ultraviolet light of the insert.
• Digestion of vector about 700 ng DNA / 10 µL volume, 1 µL 10 x NEB buffer 4, 0.5 µL EcoRI, 0.5 µL NgoMIV (NEB). Digest for 2 h to 4 h at 37 °C, afterwards inactivation for 20 min at 80 °C. Add 1 µL SAP (shrimp alcaline phosphatase) and 1.2 µL 10 x SAP buffer, incubate for 1 h at 37 °C. Clean up the vector with a PCR clean-up kit.
• Ligation: after digestion and clean-up: 50 - 100 ng of vector, 3 - 10 fold molar access of insert, 20 µL ligation volume, 2 µL T4-Ligase-Buffer, 1 µL T4-Ligase. Incubate for 20 - 30 min at room temperature, afterwards inactivation for 5 min at 70 °C. Then: store at -20 °C or transform.

Variations

• A digestion over night is possible. If you digest over night use only 0.1 µL restriction enzyme.
• It is also possible to use PCR product as insert. Digest after PCR with corresponding restriction enzymes and clean up with PCR clean-up kit. This could lead to higher yields of insert DNA because a lot of DNA gets lost during the gel electrophoresis clean up.

Restriction analysis

• Digest BioBrick of interest: about 400 ng DNA / 10 µL volume, 1 µL 10x orange buffer, 0.5 µL NotI or PstI. Digest for 2 h at 37 °C. NotI is used to determine the length of the BioBrick and the plasmid backbone, PstI is used to determine the length of the BioBrick in the plasmid backbone.
• Gel electrophoresis: add 2 µL loading buffer to every digestion mix, apply about 100 - 200 ng DNA / pocket in gel. Don't forget to apply the uncut BioBrick as well. A good agarose concentration for BioBricks between 0.2 and 3 kb is 1.5 %. The smaller your BioBrick of interest is the higher the agarose concentration should be and vice versa. The gel electrophoresis is made with TAE-buffer. Be sure that you melt your agarose gel in the same buffer you use for the electrophoresis later.

Colony PCR

Colony PCR was done with GoTaq DNA-polymerase (Promega) and BIOTAQ DNA-polymerase (Bioline)

• Pick one colony with a sterile tip and put it in one PCR tube.

• One reaction mix contains:
  • 10 µL 5x buffer
  • 2 µL MgCl₂ (25 mM stock)
  • 1 µL dNTPs
  • 0.5 µL primer mix (prefix/suffix primers or sequencing primers)
  • 35.25 µL ddH₂O
  • 0.25 µL GoTaq polymerase (Promega)
  • 1 µL template
• PCR program:
  • Start: 3 min, 98 °C
  • 30 cycles of:
    • 30 s, 98 °C
    • 30 s, 55 °C
    • 30 s / 1 kb template, 72 °C
  • Finish: 5 min, 72 °C

• Gel electrophoresis: check the fragment size
• Plate the correct colonies

Plants specific methods

Arabidopsis thaliana: Growth Conditions and Plant Material

Six weeks old A. thaliana plants, ecotype Columbia 0 (wildtype), have been gratefully offered by Patrick Treffon and Thorsten Seidel. They have been cultivated under normal day conditions (14 hours light [100 µmol ⁄ quanta m^-2s^-1] at 21°C, 10 hours darkness at 18°C). For induction of the formation of siliques the plants were shifted into long day conditions (16 hours light [100 µmol ⁄ quanta m^-2s^-1] at 21°C, 18 hours darkness at 18°C). After two weeks in long day conditions the plants have developed 2 cm long siliques. The siliques were harvested and frozen in liquid nitrogen for further use.

Arabidopsis thaliana: Total RNA Isolation

The frozen plant material has to be grinded in a precooled mortar in liquid nitrogen. About 120 mg of pulverized plant material are transfered into a precooled 2 ml Eppendorf tube and kept frozen until the following steps:

• Add 0.5 ml lysis buffer and immediately homogenize through rough shaking.
• Add 0.5 ml of saturated phenol and mix strongly.
• Add 0.5 ml of chloroform isoamyl alcohol (24:1) and vortex again at high speed for at least 30 seconds.
• Centrifugate for 5 min at 13,000 rpm.
• The lower phase contains now lipids and lipophilic compounds. The upper phase contains nucleic acids (~ 550 µl) and has to be carefully transferred into a new 2 ml Eppendorf tube. This tube has to be filled with 0.5 ml saturated phenol and 0.5 ml chloroform isoamyl alcohol (24:1). Mix immediately.
• Centrifugate at 13,000 rpm for 3 minutes.
• Prepare a new 2 ml Eppendorf tube with 1 ml of chloroform isoamyl alcohol (24:1). Transfer the upper aqueous phase (~ 540 µl) containing the protein purified nucelic acids into the new tube and vortex strongly.
• Centrifugate at 13,000 rpm for 3 minutes.
• Prepare a new 1.5 ml Eppendorf tube with 0.5 ml of pure isopropanol. For the last time transfer the upper phase (~ 400 µl) into the new tube and mix gently.
• Incubate the mixture over night at -20°C. The nucleic acids will precipitate.
• Centrifugate the samples at 13,000 rpm for 15 minutes at 4°C.
• Discard the supernatant and resuspend the pellet in 375 µl sterile H₂O.
• Add 125 µl 8 M lithium chloride and incubate for 2 hours on ice at 4°C. At this point most of the RNA is going to be precipitated.
• Centrifugate at 13,000 rpm at 4°C and discard the supernatant.
• Wash the pellet with 100 µl 70% (v/v) ethanol and discard it after centrifugation.
• Dry the pellet at room temperature.
• Dissolve the pellet in sterile H₂O (~ 25 µl, depending on the size of the pellet).
• Check the quantity and quality of the RNA with a Nanodrop spectrophotometer before starting with a cDNA synthesis.

Arabidopsis thaliana: cDNA Synthesis

After a successful total RNA isolation the RNA has to be translated in cDNA through RT-PCR:

• Take 3 µg/µl of total RNA and add sterile H₂ to 8 µl.

Additionally add

1,1 mM	Oligo-d(T)-Primer
0,83 mM	dNTPs
3,5 µl	H2O

• Vortex and centrifugate shortly.
• Incubate the samples for 10 minutes at 70°C.
• Immediately transfer the samples into ice water for 5 minutes.
• After cooling the samples centrifugate shortly.
• To start the synthesis add

6 µl	5xMMLV-Puffer
4,5 µl	H2O
1 µl	MMLV-reverse Transkriptase [200 U/µl]
0,5 µl	RNasin RNase-Inhibitor [40 U/µl]

• Mix the samples and centrifugate shortly.
• Incubate for 1 hour at 42°C to translate the RNA into cDNA.
• Transfer the samples to 70°C for 15 minutes to stop the reaction.
• The new synthesized cDNA can be used for PCR after diluting 1:10 with water. Store the cDNA at -20°C.

PCR for A.thaliana laccase ampflification

Yeast specific methods

Genomic DNA isolation

The complete genome isolation was done with the [http://www.promega.com/resources/protocols/technical-manuals/0/wizard-genomic-dna-purification-kit-protocol/ Promega Wizard genomic DNA purification system kit].