Materials and Reagents

Centrifuge tubes, polypropylene 15 ml (Beckman Coulter, catalog number: 342082 )
1.5 ml microcentrifuge tubes (Microtubes) (Corning, Axygen^®, catalog number: MCT-150-C )
1.5 ml polystyrene spectrophotometer cuvettes (KARTELL SPA CIA DELLE INDUSTRIE, catalog number: 1938 )
Ultracentrifuge thin-wall polyallomer tubes 13.2 ml (Beckman Coulter, catalog number: 331372 )
0.45 μm Millipore filter (MILLEX-HV PVDF) (EMD Millipore, catalog number: SLHV033RS )
Alumina type A-5 (Sigma-Aldrich, catalog number: A2039 )
Note: This product has been discontinued.
Micropipette tips (200 μl) (Daslab, catalog number: 162001X )
Micropipette tips (1,000 μl) (Daslab, catalog number: 162222X )
Silicone tubing (VWR, catalog number: 228-0713 )
Synechocystis sp. PCC 6803 cells (Pasteur Culture Collection of Cyanobacteria)
Milli-Q water
Distilled water
Sodium nitrate (NaNO₃) (AppliChem, catalog number: 141702 )
Sodium bicarbonate (NaHCO₃) (AppliChem, catalog number: 141638 )
Potassium phosphate dibasic (K₂HPO₄) (AppliChem, catalog number: 141512 )
Magnesium sulfate heptahydrate (MgSO₄·7H₂O) (Duchefa Biochemie, catalog number: M0513 )
Citric acid monohydrate (C₆H₈O₇·H₂O) (EMD Millipore, catalog number: 100244 )
EDTA-Na₂ (Duchefa Biochemie, catalog number: E0511 )
Calcium chloride dihydrate (CaCl₂·2H₂O) (Merck, catalog number: 2382 )
Citrate Fe-NH₄ (Sigma-Aldrich, catalog number: F5879 )
Sodium phosphate (Na₂CO₃) (Merck, catalog number: 6392 )
Boric acid (H₃BO₃) (EMD Millipore, catalog number: 100165 )
Manganese(II) chloride tetrahydrate (MnCl₂·4H₂O) (EMD Millipore, catalog number: 1059270 )
Sodium molybdate dehydrate (Na₂MoO₄·2H₂O) (Merck, catalog number: 6521 )
Zinc sulfate heptahydrate (ZnSO₄·7H₂O) (Merck, catalog number: 8883 )
Cobalt nitrate hexahydrate (Co(NO₃)₂·6H₂O) (AppliChem, catalog number: 131258 )
Copper (II) sulfate pentahydrate (CuSO₄·5H₂O) (EMD Millipore, catalog number: 102790 )
Tris ultrapure (Duchefa Biochemie, catalog number: T1501 )
Ammonium chloride (NH₄Cl) (EMD Millipore, catalog number: 101145 )
Magnesium acetate (Sigma-Aldrich, catalog number: M5661 )
β-mercaptoethanol (EMD Millipore, catalog number: 805740 )
Glycerol (AppliChem, catalog number: 131339 )
Liquid nitrogen
Trichloracetic acid (TCA) (EMD Millipore, catalog number: 100807 ) (only for Western)
Acetone (EMD Millipore, catalog number: 100014 ) (only for Western)
Ammonium chloride (EMD Millipore, catalog number: 101145 )
Sucrose (Sigma-Aldrich, catalog number: S0389 )
Hydrochloric acid fuming 47% (EMD Millipore, catalog number: 100317 )
Methanol extra pure (Scharlau, catalog number: ME0301005P )
Bovine serum albumin (BSA) (Sigma-Aldrich, catalog number: A4503 )
Protein assay dye reagent concentrate (Bio-Rad Laboratories, catalog number: 5000006 )
BG11 growth medium (see Recipes)
Extraction buffer (see Recipes)
Sucrose buffer 1 (see Recipes)
Sucrose buffer 2 (see Recipes)
60% (w/v) sucrose (see Recipes)
100% (w/v) TCA solution (see Recipes)
80% (v/v) glycerol (see Recipes)

Equipment

Fluorescent lamps
Erlenmeyer flask 250 ml (Duran Group, catalog number: 21 771 36 )
Flasks and magnetic stirrer for preparation of solutions
Orbital shaker (IKA, model: KS501 )
Roux culture bottle 1 L (Sigma-Aldrich, catalog number: CLS12901L )
Glass bottles 5 L (Iso bottle blue cap 5,000 ml) (Kavalierglass, Simax, catalog number: CFB020 )
Balances (Sartorius, catalog number: TE1502S and Precisa, model: XT120A )
pH meter (HACH LANGE SPAIN, CRISON, model: BASIC 20 )
Flow meters (ABB, model: A6200 )
Compressed air pump
Centrifuge (Beckman Coulter, model: Avanti J-25 )
Rigid polypropylene tube (Fisher Scientific, catalog number: 11723904 )
Fixed angle rotor (Beckman Coulter, model: JLA-16.250 , catalog number: 363934)
Centrifuge bottles polypropylene 250 ml (Beckman Coulter, catalog number: 356011 )
Porcelain mortar and pestle (10 cm Ø) (Fisher Scientific, catalog number: S337621 )
Sterilization oven (JP SELECTA, catalog number: 2000381 )
Autoclave (SANYO Labo Autoclave) (Panasonic Biomedical, model: MLS-3020U )
Automatic micropipettes
Vortex Mixer (Heidolph Instruments, model: Heidolph Reax 2000 )
UV-VIS spectrophotometer (Thermo Electron, model: BioMate 5 )
Fixed angle rotor (Beckman Coulter, model: JA-25.15 )
Gradient maker (Hoefer, catalog number: SG15 )
Peristaltic pump (Pharmacia Biotech, model: Pump P-1 )
Magnetic plate stirrer (Cole-Parmer, catalog number: EW-04807-45 )
Ultracentrifuge (Beckman Coulter, model: XL-80 )
Swinging-bucket rotor (Beckman Coulter, model: SW 41 Ti )
ISCO UA-6 detector UV/VIS (Density Gradient Fractionator, Teledyne Isco, catalog number: 67-9000-176 ) with TRIS^TM pump (Teledyne Isco)
Microcentrifuge (Eppendorf, model: 5424/5415 R )
Thermoblock (Eppendorf Thermomixer compact) (only for Western)
Metal connectors (Parker-Legris, catalog number: 0180 04 00 )
CO₂ cylinder containers

Procedure

An overview of the whole protocol, divided in four steps, is shown in Figure 1.

Figure 1. Scheme of the complete procedure described in the protocol

Cultivation of Synechocystis
1. Grow Synechocystis cells photoautotrophically at 30 °C in BG11 medium (Rippka et al., 1979) supplemented with 1 g L^-1 of NaHCO₃ (BG11C) under continuous illumination (50 µmol of photons m^-2 sec^-1, white light from fluorescent lamps).
2. Estimation of growth phase
  A volume of 3-5 L of cells, in exponential or stationary growth phase depending on the purpose of each experiment, is used. Growth phase is estimated by measuring total chlorophyll content in methanolic extracts of cells (McKinney, 1941).
3. Harvest cells
Breakage and fractionation of Synechocystis cells
1. Pre-treatment
  All glass materials, porcelain mortar and pestle were heated in a sterilization oven at 200 °C for 3 h and all plastic materials were autoclaved at 121 °C for 20 min.
  Note: RNase-free water was used to prepare all buffers.
2. Breakage of Synechocystis cells
  Place in a pre-chilled porcelain mortar the same weight of cells and alumina. Put the mortar on top of an ice bucket with ice. Mix with the pestle and once the cells and the alumina are well mixed continue grinding for 2 min. Add around 20 ml extraction buffer (1 or 10 mM Mg-acetate) with β-mercaptoethanol added immediately before use.
3. Fractionation of Synechocystis cells
  Recover as much material as possible in two polypropylene tubes of 15 ml. Centrifuge at 10,000 x g for 10 min in a JA-25.15 rotor at 4 °C to eliminate the alumina, the cell debris and the unbroken cells. Transfer the supernatant into new 15 ml tubes and centrifuge at 30,000 x g for 30 min in the same rotor at 4 °C. This centrifugation is required to completely eliminate membranes.
4. Freezing reserve
  Dispense aliquots from the supernatant of this centrifugation step (S30 fraction) in 1.5 ml Eppendorf tubes with 5% (v/v) glycerol. For this process, place the 1.5 ml tubes on ice and add 40 µl of 80% (v/v) glycerol and 600 µl of the S30 fraction to each tube. Mix gently, using a micropipette, and rapidly freeze the tubes in liquid nitrogen. Before freezing reserve an aliquot to determine the total protein amount of this S30 fraction by the standard method of Bradford, using albumin bovine as reference (Bradford et al., 1976). Usually 10-15 µg/µl of total protein concentration is obtained in S30 fraction.
  Notes:
  1. When extraction buffer and gradient solutions contain 1 mM Mg-acetate (low Mg²⁺), most bacterial ribosomes are dissociated into 30S and 50S subunits but when using 10 mM Mg-acetate (high Mg²⁺), in the buffers and solutions, the 70S vacant ribosome peak is mainly observed.
  2. It is worth noting that in cyanobacteria, phycobiliproteins represent around 30% of total protein concentration. This fact must be taken into account when considering the amount of the S30 fraction needed for the next step of this procedure.
  3. The S30 fraction can be stored as different aliquots at -80 °C to load separate gradients on different days. This is a backup in case there is any problem in later steps of the protocol, especially in the centrifugation, fractionation or generation of the gradient profiles.
Preparation of sucrose gradients and ultracentrifugation
1. Preparation of sucrose gradients
2. Ultracentrifugation
  1. Gently layer the S30 fraction (100-300 µl) on top of the 10-30% sucrose gradient using a micropipette and via single drops close to the surface of the sucrose gradient.
  2. Centrifuge at 77,175 x g, for 8 h at 2 °C in a pre-cooled Beckman ultracentrifuge in the SW 41 Ti rotor.
Isolation of ribosomal particles
1. Carefully remove the gradient tubes from the centrifuge and completely fill each tube with Milli-Q water before placing it in the ISCO fractionation system.
2. Fractionate the gradient from the top using 60% (w/v) sucrose to push the content of the tube toward the UV detector (A₂₅₄), with the TRIS^TM pump (flow rate 1 ml/min). Turn on the recorder (1 cm/min, sensitivity 1) to obtain the sucrose gradient profile while the fractions (0.5 ml) are manually collected.
3. Place the fractions in a container with liquid nitrogen, as they are collected, to freeze them quickly and then store at -80 °C until use.
  Representative examples of the expected profiles are shown in Figure 2.
  
  Figure 2. Sedimentation profiles showing the free subunits and 70S vacant ribosomes. The Synechocystis S30 supernatant was fractionated on a 10-30% sucrose density gradient in the presence of 1 mM (A) or 10 mM (B) Mg²⁺. Small numbers refer to collected fractions. Adapted from (Galmozzi et al., 2016).
4. The treatment of the fractions from this point depends on the use that will be given to them. In the case of analysis by Western blot, precipitate the total protein with 100% (w/v) TCA (see Recipes).

Notes

Nowadays the analog signal from the ISCO UA-6 detector can be transformed into a digital signal using a Bus-Powered Multifunction DAQ USB Device (NI USB-6008) from National Instruments.

Recipes

BG11 growth medium (Rippka et al., 1979)

BG11C (1 L)
1.5 g NaNO₃
1 g NaHCO₃
0.2 ml 1 M K₂HPO₄
10 ml concentrate BG11 (see below)
Autoclave at 121 °C, 1 atm for 20 min
Concentrate BG11
7.5 g/L MgSO₄·7H₂O
0.6 g/L citric acid
0.1 g/L EDTA-Na₂
100 ml A5 solution (see below)
3.6 g/L CaCl₂·2H₂O
0.6 g/L citrate Fe-NH₄
2 g/L Na₂CO₃
A5 solution
2.86 g/L H₃BO₃
1.81 g/L MnCl₂·4H₂O
0.31 g/L Na₂-MoO₄·2H₂O
0.22 g/L ZnSO₄·7H₂O
0.05 g/L Co(NO₃)·6H₂O
0.08 g/L CuSO₄·5H₂O

Extraction buffer
20 mM Tris-HCl, pH 8.0
1 or 10 mM Mg-acetate
20 mM NH₄Cl
5 mM β-mercaptoethanol (added just prior to use)
This solution (lacking the β-mercaptoethanol) was autoclaved at 121 °C, 1 atm for 20 min
Sucrose buffer 1
20 mM Tris-HCl, pH 8.0
1 or 10 mM Mg-acetate
20 mM NH₄Cl
10% (w/v) sucrose
5 mM β-mercaptoethanol (added just before use)
Sucrose buffer 2
20 mM Tris-HCl, pH 8.0
1 or 10 mM Mg-acetate
20 mM NH₄Cl
30% (w/v) sucrose
5 mM β-mercaptoethanol (added just before use)
Sucrose buffer 1 and 2 are prepared from autoclaved RNase free stocks and sucrose was dissolved at the end
60% (w/v) sucrose
Prepared with Milli-Q water and heating. Once the sucrose is dissolved the volume is adjusted with a test tube
100% (w/v) TCA solution
To a previously unopened bottle containing 500 g of TCA, add 227 ml of sterile Milli-Q water. The resulting solution will contain 100% (w/v) TCA
80% (v/v) glycerol
Prepared with Milli-Q water and autoclaved at 121 °C, 1 atm for 20 min

Note: All solutions are stored at 4 °C.

Acknowledgments

This protocol was adapted and modified from previously published studies by Sugita et al. (2000). We are grateful to Dr. J. de la Cruz for his expert advice, helpful discussions and a critical reading of the manuscript. We thank M. Roldán for technical assistance. This work was supported by Junta de Andalucía (grant P07-CVI-02792 and group BIO-284) and Spanish Ministerio de Economía y Competitividad (MINECO) and Fondo Social Europeo (FSE) (grant BFU2013-41712-P).

References

Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72: 248-254.
Galmozzi, C. V., Florencio, F. J. and Muro-Pastor, M. I. (2016). The cyanobacterial ribosomal-associated protein LrtA is involved in post-stress survival in Synechocystis sp. PCC 6803. PLoS One 11(7): e0159346.
McKinney, G. (1941). Absorption of light by chlorophyll solution. J Biol Chem 140:315-21.
Mutsuda, M. and Sugiura, M. (2006). Translation initiation of cyanobacterial rbcS mRNAs requires the 38-kDa ribosomal protein S1 but not the Shine-Dalgarno sequence: development of a cyanobacterial in vitro translation system. J Biol Chem 281(50): 38314-38321.
Rippka, R., Deruelles, J., Waterbury, J. B., Herdman, M. and Stanier, R. Y. (1979). Generic assignments, strain histories and properties of pure cultures of cyanobacteria. J Gen Microbiol 111: 1-61.
Sato, N., Wada, A. and Tanaka, A. (1998). Ribosomal proteins in the cyanobacterium Anabaena variabilis strain M3: presence of L25 protein. Plant Cell Physiol 39(12): 1367-1371.
Sugita, C., Sugiura, M. and Sugita, M. (2000). A novel nucleic acid-binding protein in the cyanobacterium Synechococcus sp. PCC6301: a soluble 33-kDa polypeptide with high sequence similarity to ribosomal protein S1. Mol Gen Genet 263(4): 655-663.