Autolysin Production from Chlamydomonas reinhardtii

Materials and reagents

1. 90 mm Petri dishes

2. Inoculating loop

3. Sterile 50 mL centrifuge tubes

4. Cell scraper

5. Pipette tips

6. 1.7 mL microcentrifuge tubes

7. 50 mL conical tubes

8. 50 mL Luer-lock syringe

9. 0.45 μm PES filter (VWR, catalog number: 76479-020)

10. Permanent marker pen

11. Microscope slides with eight wells (75 mm × 25 mm) (MP Biomedicals, catalog number: 096040805)

12. Plastic spectrophotometer cuvette (VWR, catalog number: 97000-586)

13. 1 L filtration unit (VWR, catalog number: 10040-440)

14. Mating type (MT)+ wildtype strain CC-125 (available from the Chlamydomonas Resource Center, www.chlamy.org)

15. MT- wildtype strain CC-124 (available from the Chlamydomonas Resource Center, www.chlamy.org)

    Note: Other pairs of MT+/MT- strains can be used; CC-620/621 are usually recommended due to their high mating efficiency.

16. Cell wall–less wildtype strain CC-503 (cw92, available from the Chlamydomonas Resource Center, www.chlamy.org)

17. Ammonium chloride (NH₄Cl) (Sigma, catalog number: A9434)

18. Sodium chloride (NaCl) (Sigma, catalog number: 746398)

19. Calcium chloride dihydrate (CaCl₂·2H₂O) (Sigma, catalog number: C3881)

20. Magnesium sulfate heptahydrate (MgSO₄·7H₂O) (Sigma, catalog number: 63140)

21. Tris base (J.T. Baker, catalog number: 4099-07)

22. Potassium phosphate monobasic (KH₂PO₄) (J.T. Baker, catalog number: 3246-07)

23. Potassium phosphate dibasic (K₂HPO₄) (J.T. Baker, catalog number: 3252-07)

24. Ethylenediaminetetraacetic acid disodium salt dihydrate (Na₂EDTA·2H₂O) (Sigma, catalog number: E5134)

25. Iron (II) sulfate heptahydrate (FeSO₄·7H₂O) (Sigma, catalog number: F-8048)

26. Zinc sulfate heptahydrate (ZnSO₄·7H₂O) (Sigma, catalog number: Z0251)

27. Boric acid (H₃BO₃) (Sigma, catalog number: B6768)

28. Manganese (II) chloride tetrahydrate (MnCl₂·4H₂O) (Sigma, catalog number: 221279)

29. Copper (II) chloride dihydrate (CuCl₂·2H₂O) (Sigma, catalog number: 467847)

30. Sodium molybdate dihydrate (Na₂MoO₄·2H₂O) (J.T. Baker, catalog number: 3764)

31. Cobalt (II) chloride hexahydrate (CoCl₂·6H₂O) (Sigma, catalog number: C2644)

32. Glacial acetic acid (Sigma, catalog number: 320099)

33. Triton X-100 (Sigma, catalog number: T-9284)

34. Granulated agar (Fisher Scientific, catalog number: BP9744-5)

35. 0.1% Triton X-100 (see Recipes)

36. Sucrose (Sigma, catalog number: S0389)

37. Stock solutions

    1. Salts +N solution (20×) (see Recipes)

    2. Salts -N solution (20×) (see Recipes)

    3. 2 M Tris Base (100×)

    4. Phosphate buffer (200×) (see Recipes)

    5. Hutner’s trace elements (200×) (see Recipes, also available from the Chlamydomonas Resource Center, www.chlamy.org)

38. TAP (Tris-Acetate-Phosphate) liquid medium (see Recipes)

39. TAP 1.5% agar medium (see Recipes)

40. TAP -N liquid medium (see Recipes)

41. TAP sucrose 40 mM (see Recipes)

Equipment

1. Pipettes

2. Centrifuge and microcentrifuge

3. Light microscope

4. Laminar flow hood

5. Glass beaker

6. Spectrophotometer

7. Vacuum pump

Procedure

1. Cell growth

   1. Spread MT+ (CC-125) and MT- (CC-124) cells on TAP 1.5% agar medium using an inoculating loop (approximately two loop-full of cells spread over the whole surface).

   2. Incubate for 7–10 days in bright light (lid facing down, 22 °C, ~100 μmoles m^-2·s^-1) (Figure 1).

      
      

      
      Figure 1. Plates of Chlamydomonas CC-124 (MT-) and CC-125 (MT+) cells grown on TAP agar plate at harvesting time. Two loop-full of cells were spread over the plate and grown under bright light (100 μmoles m^-2·s^-1) for seven days.




2. Gametogenesis

   1. Start this step in the late afternoon (5:00–6:00 PM).

   2. For each plate, add 10 mL of TAP -N liquid medium to a sterile 50 mL centrifuge tube (use one tube per plate).

   3. Using a cell scraper, transfer the cells from the agar to the liquid.

   4. Use a pipette to resuspend cell clumps as much as possible (Figure 2).

      
      

      
      Figure 2. Cell suspension after transfer from TAP agar plates to TAP -N liquid medium. Cells were scraped from plate and resuspended in liquid medium (here, MT- CC-124 on the left and MT+ CC-125 on the right). Pipetting is used to break cell clumps as much as possible.

      
      

   5. Leave horizontally in bright light (~100 μmoles m^-2·s^-1) overnight without shaking.




3. Mating and autolysin production

   1. In the morning, transfer 10 μL of cells to a microscope slide and check for motility.

      Note: Over 50% of cells should be moving actively.

   2. Mix the MT+ and MT- strains in the 50 mL centrifuge tubes and incubate for 2 h in the dark without shaking.

   3. Centrifuge at 3,000× g for 5 min.

   4. Transfer supernatant to a clean glass beaker and discard the tube containing the pellet.

   5. Filter the supernatant into a sterile 50 mL centrifuge tube using a 50 mL syringe and a 0.45 μm PES filter.

   6. Set aside 2 mL of filtered supernatant for Section D and place the rest to freeze immediately in a -80 °C freezer.




4. Testing autolysin preparation efficiency

   1. Four days prior to autolysin production, inoculate CC-125 (cell walled) and CC-503 (cell wall–less) strains in 5 mL of TAP liquid medium in a 50 mL conical tube.

      Note: Any cell wall–less strain (cw15 or cw92 mutant) can be used as a control for lysis. After detergent treatment (step D10), it should show a white pellet and a green supernatant. CC-5325/CC-4533, which is annotated cw15, synthesizes a cell wall and should not be used for that purpose (Zhang et al., 2022).

   2. Harvest the 5 mL of late log CC-125 and CC-503 cells and adjust each OD_750nm to 0.3 with fresh TAP -N medium.

   3. To evaluate lysis efficiency by chlorophyll absorbance, transfer 1 mL to a cuvette and measure OD_662nm of the initial cell suspensions (OD1, zero with TAP -N medium).

   4. Centrifuge 4 × 1 mL of CC-125 and 2 × 1 mL of CC-503 at 1,500× g for 5 min in 1.7 mL centrifuge tubes.

   5. Discard the supernatants.

   6. Resuspend the two pellets of CC-503 in 1 mL each of TAP -N (positive control), two pellets of CC-125 in 1 mL each of TAP -N liquid medium (negative control), and the two other CC-125 pellets in 1 mL each of the autolysin preparation supernatant set aside in step C6. We now have six tubes for three conditions: cell wall–less CC-503, cell-walled CC-125 in TAP -N, and cell-walled CC-125 treated with the prepared autolysin.

   7. Incubate horizontally for 45 min in bright light (~100 μmoles m^-2·s^-1) without shaking.

   8. Centrifuge all the tubes at 1,500× g for 5 min.

   9. Discard the supernatants.

   10. For each condition, resuspend tube 1 in 1 mL of water and tube 2 in 1 mL of 0.1% Triton X-100.

   11. Vortex for 2 min.

   12. Centrifuge at 1,500× g for 5 min.

   13. Autolysin efficiency can be quickly assessed from the color of the pellets and supernatants (Figure 3). After Triton X-100 treatment, the supernatant in the CC-125 cells treated with efficient autolysin is green, and we can proceed with the quantification of lysis efficiency. If it is still translucent, the autolysin preparation failed, and all tubes should be discarded.

       
       

       
       Figure 3. Expected results from autolysin and detergent treatment. Cells incubated with the prepared autolysin or in control conditions were treated with the detergent Triton X-100 to induce cell lysis. Cell wall–less cells (CC-503) display a green supernatant showing cell lysis and release of chlorophyll, while the pellet becomes white (B). Cell-walled cells (CC-125) incubated in control conditions are resistant to the detergent and the cell pellet stays green (D). Cells treated with good autolysin undergo at least partial lysis and display a green supernatant (F).

   
   

   14. Transfer the supernatant to a cuvette and measure OD_662nm (OD2, zero with 0.1% Triton X-100).

   15. Calculate gross efficiency by the ratio between the OD_662nm after (OD2) and before (OD1) detergent treatment:

       
       

       Efficiency (%) = OD2_662nm/OD1_662nm




5. Using the autolysin preparation

   1. Thaw the frozen autolysin in a beaker filled with water at room temperature for ~1 h.

      Note: We recommend using the freshest preparation possible. Avoid using autolysin stored for more than two months, as it will significantly lose activity over time.

   2. Centrifuge cells to transform at 1,500× g for 5 min.

   3. Discard the supernatant.

   4. Resuspend the pellet in autolysin solution at ~5 × 10⁶ cells/mL.

   5. Incubate in bright light (~100 μmoles m^-2·s^-1) without shaking for 45 min.

   6. Centrifuge at 1,500× g for 5 min.

   7. Discard the supernatant.

   8. Resuspend the pellet in 25 mL of TAP sucrose 40 mM.

   9. Centrifuge at 1,500× g for 5 min.

   10. Discard the supernatant.

   11. Proceed with the transformation protocol.

Data analysis

All samples not treated with Triton X-100 are expected to show a clear supernatant and a dark green pellet (Figure 3A, 3C, and 3E). After Triton X-100 treatment, the cell wall–less strain CC-503 will show a green supernatant and a white pellet (Figure 3B). On the contrary, the CC-125 control cells that were incubated in TAP -N display a clear supernatant and a dark green pellet like the untreated cells (Figure 3D). This is because the control cells are still protected by their cell wall, while the CC-503 strain is highly susceptible to lysis due to the absence of the cell wall and releases its chlorophyll content in the supernatant after detergent treatment. If the preparation works, the CC-125 cells treated with autolysin and Triton X-100 will show a similar result to the cell wall–less strain. Depending on the quality of the autolysin preparation, part of the pellet can still be green; in this case, serial treatment of cells to be transformed can be necessary. If no white pellet is observed, discard the frozen autolysin tube.

Note: Sometimes, the pellet from autolysin-treated cells will appear partly white even without detergent treatment because vortexing is harsh enough to lyse cell wall–less cells.

To ensure the best quality of autolysin, cell lysis efficiency can also be quantified by measuring chlorophyll release in the supernatant. The best result will be reached when the ratio of OD_662nm after lysis over OD_662nm before lysis is the closest to the value obtained with the cell wall–less strain. In Table 1, we provide an example of efficiency of chlorophyll release obtained from cell wall–less cells (CC-503) and from untreated cell-walled cells (CC-125), showing the difference observed between lysed and intact cells.

Table 1. Quantification of chlorophyll release by detergent treatment. Example of quantification of chlorophyll release in the supernatant from cell wall–less (CC-503) and cell-walled (CC-125) cells treated with Triton X-100.

Validation of protocol

Autolysin prepared using this protocol has been used to generate targeted mutants by CRISPR/Cas9 in the TPT2 and TPT3 genes of Chlamydomonas reinhardtii (Huang et al., 2023). This protocol was also used for preparation of CC-124 cells prior to insertional mutagenesis and phenotypic screen for starch catabolism mutants (Tunçay et al., 2013).

Recipes

1. 0.1% Triton X-100 (for 100 mL)

   100 μL of Triton X-100

   Complete with distilled water

   Store at room temperature




2. Stocks solutions

   Salts +N solution (for 1 L, 20×)

   150 mM NH₄Cl

   16.6 mM MgSO₄·7H₂O

   6.8 mM CaCl₂·2H₂O

   Complete with distilled water

   Store at room temperature

   
   

   Salts -N solution (for 1 L, 20×)

   150 mM NaCl

   16.6 mM MgSO₄·7H₂O

   6.8 mM CaCl₂·2H₂O

   Complete with distilled water

   Store at room temperature

   
   

   2 M Tris base (for 1 L, 100×)

   2 M Tris base

   Complete with distilled water

   Store at room temperature

   
   

   Phosphate buffer (for 1 L, 200×)

   687 mM KH₂PO₄

   362 mM K₂HPO₄

   Complete with distilled water

   Store at room temperature

   
   

   Hutner’s trace elements (for 1 L, 200×)

   800 mL of distilled water

   27 mM Na₂EDTA·2H₂O

   Adjust pH to 6.5 with NaOH

   3.6 mM FeSO₄·7H₂O

   15 mM ZnSO₄·7H₂O

   37 mM H₃BO₃

   5.2 mM MnCl₂·4H₂O

   1.3 mM CuCl₂·2H₂O

   1.1 mM Na₂MoO₄·2H₂O

   1.3 mM CoCl₂·6H₂O

   Complete with distilled water

   Autoclave for 30 min at 120 °C

   The solution’s color is light green after mixing all the powders. Let the solution oxidize for a week in the dark. It will turn orange, brown, and then purple

   Store at room temperature in obscurity




3. TAP medium (for 1 L)

   800 mL of distilled water

   50 mL of +N Salt solution

   10 mL of tris base

   5 mL of phosphate buffer

   5 mL of Hutner’s trace elements

   1 mL of glacial acetic acid

   Check pH range 7–7.2

   Complete to 1 L with distilled water

   Autoclave for 30 min at 120 °C




4. TAP 1.5% agar medium (for 1 L)

   800 mL of distilled water

   50 mL of salt +N solution

   10 mL of Tris Base

   5 mL of phosphate buffer

   5 mL of Hutner’s trace elements

   1 mL of glacial acetic acid

   Check pH range 7–7.2

   Complete to 1 L with distilled water

   15 g of agar

   Autoclave for 30 min at 120 °C




5. TAP -N medium (for 1 L)

   800 mL of distilled water

   50 mL of salt -N solution

   10 mL of tris base

   5 mL of phosphate buffer

   5 mL of Hutner’s trace elements

   1 mL of glacial acetic acid

   Check pH range 7–7.2

   Complete with distilled water

   Autoclave for 30 min at 120 °C




6. TAP sucrose (for 1 L)

   40 mM sucrose

   Complete with TAP liquid medium

   Filter sterilize

Acknowledgments

I am thankful to Neda Fakhimi, Sai Madireddi, and Carolyne Stoffel for feedback on this protocol. I acknowledge David Dauvillée from whom I adapted this protocol. This work was supported by the Carnegie Institution for Science, Department of Plant Biology.

Competing interests

I declare no competing interests.

References

1. Huang, W., Krishnan, A., Plett, A., Meagher, M., Linka, N., Wang, Y., Ren, B., Findinier, J., Redekop, P., Fakhimi, N., et al. (2023). Chlamydomonas mutants lacking chloroplast TRIOSE PHOSPHATE TRANSPORTER3 are metabolically compromised and light-sensitive. Plant Cell. doi: 10.1093/plcell/koad095.
2. Hwang, H. J., Kim, Y. T., Kang, N. S. and Han, J. W. (2018). A Simple Method for Removal of the Chlamydomonas reinhardtii Cell Wall Using a Commercially Available Subtilisin (Alcalase). J Mol Microbiol Biotechnol 28(4): 169-178.
3. Kindle, K. L. (1990). High-frequency nuclear transformation of Chlamydomonas reinhardtii. Proc Natl Acad Sci U S A 87(3): 1228-1232.
4. Matsuda, Y. and Kubo, T. (2004). Gametolysin. In: Handbook of Proteolytic Enzymes (2^nd Edition). Academic Press, 592-595.
5. Shin, S. E., Lim, J. M., Koh, H. G., Kim, E. K., Kang, N. K., Jeon, S., Kwon, S., Shin, W. S., Lee, B., Hwangbo, K., et al. (2016). CRISPR/Cas9-induced knockout and knock-in mutations in Chlamydomonas reinhardtii. Sci Rep 6: 27810.
6. Tunçay, H., Findinier, J., Duchêne, T., Cogez, V., Cousin, C., Peltier, G., Ball, S. G. and Dauvillée, D. (2013). A forward genetic approach in Chlamydomonas reinhardtii as a strategy for exploring starch catabolism. PLoS One 8(9): e74763.
7. Zhang, N., Pazouki, L., Nguyen, H., Jacobshagen, S., Bigge, B. M., Xia, M., Mattoon, E. M., Klebanovych, A., Sorkin, M., Nusinow, D. A., et al. (2022). Comparative Phenotyping of Two Commonly Used Chlamydomonas reinhardtii Background Strains: CC-1690 (21gr) and CC-5325 (The CLiP Mutant Library Background). Plants 11(5): 585.