Vitrifying hyphae in DMSO, glycerol, and basal medium
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Introduction

Cryptobiosis describes the suspended animation that some microbes enter under adverse conditions such as drought, cold, and lack of oxygen. The kingdom fungi possesses a relatively well conserved and multifunctional signalling network called the Mitogen Activated Protein Kinase (MAPK) pathways that respond to changes in osmosis, light, pH, pheromones, etc.

This paper examines the physical chemical properties of supercooled aqueous solutions, and the physiological tolerances of filamentous fungi, to develop an inexpensive storage medium. The parameters for success in this experiment include confirming that cultures are not only alive, but can also produce fruitbodies and spores upon revival.

Successful long-term culture storage is critical to any serious mushroom-related endeavor. For basidiomycete (mushroom forming) fungi it remains an open problem. The basidiomycete MAPK network, similar but different among species, is also implicated in

  • cell morphology (highly variable from spore to shroom);
  • sexual reproduction, including fruiting ability; and
  • secondary metabolites of possible clinical significance.

My prior work on long-term storage diybio/water-cultures and diybio/perlite-protocol describes useful lessons in the state of the art. This paper describes a novel medium informed by mammal flesh storage that

  • uses a combination of nontoxic cryoprotectants like DMSO, glycerol, and tetralose;
  • has a glass transition temperature around –20 °C for cell vitrification;
  • quickly changes to a liqid at room temperature, allowing convenient revival;
  • provides essential nutrients with low quantities of basal sugar and salt; and
  • requires no specific equipment or recurring costs to successfully reproduce.

The medium should exhibit ideal properties at –20 °C, exert just enough osmotic stress to force hardship metabolism, and not otherwise starve the fungi. A member of the Shroomery's PhD tribe inspired this work, suggesting that "sometimes the deep freeze isn't the answer."

What's in the tubes: DMSO coats fungal hyphae while glycerol disrupts ice crystal tetrahedra. Dissolved sugar and salt buffer the solution and provide essential nutrients.

Materials and methods

The light malt extract (CBW Bavarian Wheat) came from Breiss Malt & Ingredients in Chilton, WI. The DMSO (99.5% GC, batch 015K0151) came from Sigma-Aldrich in St. Louis, MO. The glycerol (№ GRM081-1L) came from HiMedia. The cryotubes (№ 430658) came from Corning in Corning, NY.

Developing a test medium

I made blank tubes, standard 1.5 mL Eppendorfs, to produce multivariate freeze point data. Equipment that measures ice granulation is beyond my grasp, so I reconstructed hypothetical curves from 30 data points.

Note that I used binary data (frozen or not?) and macro inspection (relative crystallization?) to estimate the curves. All the measures below are in % w/v per 1 mL deionized water. The basal saline is 50:50 sea salt and light malt extract.

DMSO × Glycerol × Saline
5%
15% 10% 0.9% NaCl
15% 0.6% basal
20% 20% 0.3% basal
25%

I established scaled-down quantities to 1 mL test tubes with Aqua-Calc's conversion tools. None of the tubes were made in a sterile environment, so random cells existed to act as possible granulation points.

The real value of the parameters is error-tolerant ±5 °C as long as the inoculated solution remains viscous and not crystals. The tradeoff is between a simple formula that works, and a precise one that targets the exact glass transition temperature.

The main physical parameters I considered were freezing point by weight, osmotic pressure and related measurements like gravity and water potential, and the miscibility and solubility in water. DMSO lowers the freezing point and glycerol disrupts crystals.

Measuring the chemical properties

Pressure. Fungi normally maintain internal turgor pressures around 600 kPa at room temperature (293 K). http://www.yorku.ca/planters/Mycota_Review.pdf

The molarity of the solutes was 2.55984 M (20% DMSO), 1.08585 M (10% glycerol), and 0.05133 M (0.3% saline). To estimate the osmotic stress of combined solutes at 253.15 K on a typical terrestrial fungus, I used the below version of the ideal gas law.

π = MRT, where

π = osmotic pressure in atm
M = molar concentration in mol/L
R = normal gas constant, 0.08206 L·atm/K·mol
T = absolute temperature in K

Unsure of how volume affects osmolarity, I used R. Nave's HyperPhysics calculator to 1 mL volumes, what will be in each tube:

  • 0.020g DMSO, 538.79898 kPa
  • 0.010g glycerol, 228.55107 kPa
  • 0.003g saline, 108.04467 kPa

The combined osmotic pressure is 875.39472 kPa. Subtracting the 600 kPa internal pressure associated with active growth, this leaves 275.39472 kPa of environmental stress in an otherwise unpressurized environment, within and without.

That stress is about 46% of the reference 600 kPa, suggesting that hyphae will be squeezed to about 54% their normal size. The fungi themselves will mitigate this to a degree by taking in glycerol and producing it themselves.

Given that fungi are known to survive in up to 5M NaCl, the effects seem gentle enough in terms of adverse conditions. Nobody wants to be stuffed into a supercold tube with DMSO making you taste garlic.

Freezing Point. I votexed the tubes for 5s and arranged them away from the edges of a freezer box. I put the box in a –20 °C freezer and waited for the ice question to resolve.

After two weeks, I vortexed the unfrozen tubes 2s to induce crystals. None of the manhandled tubes spontaneously froze.

Several tubes had fully formed snowflakes inside. todo: Photograph a snowflake tube.

pH. todo: Write up beer/wine strip results and test the pH with a real meter.

Gravity. todo: Test the gravity with a hydrometer.

Freezing Point Data for DMSO Water Solutions from Gaylord Chemical

Preparing the culture tubes

This section happened in my capable and adaptive home lab due to a public health crisis. Please see diybio/grow-shrooms for more details.

I revived my culture collection agar slant → plate → broth. I also made all tubes in duplicate and washed the cells in cryo medium The ingredients were, per 100 mL dH2O,

  • 0.15g sea salt,
  • 0.15g light malt extract,
  • 25.24 mL DMSO, and
  • 11.2 mL glycerol.

I fermented the mushroom cultures for 1 week in light malt extract broth (20 g/L LME). This is half the usual fermentation time (2 weeks broth to substrate). I aimed to capture the mycelium at the cusp of exponentiality.

The fermentation vessels were Mason jelly jars (4 oz) with about 25 mL sterile broth. The lab paradigm uses the same containers for 2D and 3D colonies on agar and broth, respectively. Readily available, reusable, stackable, and discreet.

I divided the colonized broth among 12 tubes to capture the mycelium. I centrifuged them in an Eppendorf 5415 C for 10 min at 10 kRPM after Okamura's example.1 Then I manually consolidated the pellets into 2 tubes with sterile toothpicks.

To wash the mycelium, I added 1 mL cryo medium and vortexed the samples Then I centrifuged for 2 min at 10 kRPM and discarded the supernatant. I repeated this step 4 more times for a total of 5 washes. Finally I spun the tubes dry and pipetted out the lingering medium.

When the pellets were no longer soaked, I used toothpicks to transfer them to cryotubes. The specs are legit and comparable to more expensive Nalgene tubes: 1.2 mL volume, silicon washer system, externally threaded.

Then I added 1 mL fresh medium, vortexed them, and placed them in mini freezer boxes between ice packs to stabilize the temperature. This is a necessary precaution for home freezers with an auto-defrost mechanism, as temperature fluctuation is harmful. I inoculated test plates variously with 5, 10, and 20 µL solution (200, 100, and 50 revivals per tube).

Results and discussion

The goal was to find a ratio of DMSO, glycerol, and media that behaved like a thick liquid or gel at –20 °C and vitrified the cells. Additionally, the solution had to exert the minimum osmotic stress necessary to activate the Hog1 (high osmolarity glycerol) orthologues of diverse fungi.

20% DMSO : 10% glycerol : 0.3% sugar/salt

Please see the hypothetical curves below and note that the data isn't "measured" in a meaningful sense. It's reconstructed from yes/no freezing data, along with visual inspection of the ice crystals.

I interpret the curves like zooming in on one part of the wider DMSO : water freeze point curve. I believe more irregularities will appear (e.g., the red line) the closer and more precisely you look.

Please do take the curves with a grain of salt becaue they represent educated guesses and not measurements. The observed frozen tubes seem to suggest that dissolved salts inhibit DMSO's antifreeze power to a degree.

The outlined box is the "target zone" of freezing temperatures below –20 °C using the least possible glycerol. Its gravity is too strong relative to its antifreeze power to use too much of.

Estimated (sketchy) and observed (solid) curves for 30 possible cyro formula

5th generation results

The 5th generation continues the work at diybio/water-cultures, which itself continues the work at AndyHinton's Journal. The progression is dH2O → saline → basal saline → basal cryo in modified dram vials → blood serum tubes → cryotubes. For the table below,

  • Tubes 01–24 are numbered alphabetically as of 2020-04-01, the last time I took full stock and the epoch for my collection.
  • Tubes 25–n are numbered in the order processed and may appear out of alphabetical order.
  • The HexID is an arbitrary string used for general tagging and tracking across different platforms.
  • 🔬 denotes whether polarized light microscopy data exists for the mycelium before and after storage.
  • 🧬 denotes whether Sanger sequencing data exists for the NS7/ITS4 region from diybio/fungi-barcodes.
Tube Vital Binomial Common Strain Date P Value HexID Notes
01 ? Aspergillus niger black mold Carolina 2019-09-21 P-1 3D5D 🔬 🧬
02 ? Coprinus comatus shaggy mane 2019-10-09 P-2 4C9B 🔬 🧬
03 ? Cyclocybe aegerita poplar mushroom 2018-04-10 P-5 DFC6 🔬 🧬
04 ? Fomitopsis betulina birch polypore Mass Mushroom Fest '19 2019-10-09 P-2 34CA 🔬 🧬
05 ? Ganoderma curtisii gold reishi Ryan Paul Gates 2019-03-07 P-1 867A 🔬
06 ? Ganoderma lucidum lingzhi reishi Ryan Paul Gates 2018-02-10 P-1 49E3 🔬 🧬
07 ? Ganoderma sessile Ryan Paul Gates · HW 2018-02-03 P-1 5763 🔬 🧬
08 ? Grifola frondosa hen of the woods Charles River 2018-12-29 P-2 CD38 🔬 🧬
09 ? Grifola frondosa hen of the woods Fat Moon Farm 2018-02-10 P-1 8DE3 🔬 🧬
10 ? Hericium abietis bear's head 2019-09-21 P-4 BC2B 🔬 🧬
11 ? Hericium coralloides Bryant Homestead 2019-09-21 P-2 7D68 🔬 🧬
12 ? Inonotus obliquus chaga leschampignons · Wild 2019-09-21 P-1 6254 🔬 🧬
13 ? Ischnoderma resinosum benzoin bracket Bryant Homestead 2018-02-10 P-1 7873 🔬 🧬
14 ? Laetiporus sp. chicken of the woods 2018-03-31 P-1 BC74 🔬
15 ? Lentinula edodes shiitake 3782 2018-02-10 P-4 0F8C 🔬 🧬
16 ? Penicillium roqueforti blue cheese mold 2019-09-21 P-2 3626 🔬 🧬
17 ? Pholiota microspora nameko JPN 2019-09-21 P-1 42FD 🔬 🧬
18 ? Pholiota microspora nameko Mycoterra Farm 2018-11-20 P-7 39D9 🔬 🧬
19 ? Pleurotus columbinus blue oyster Mycoterra Farm 2018-11-20 P-5 0586 🔬 🧬
20 ? Pleurotus eryngii king trumpet 2019-02-26 P-1 E48E 🔬 🧬
21 ? Pleurotus ostreatus pearl oyster Black Pearl 2019-10-09 P-2 ACEA 🔬 🧬 Chinese GMO pirate strain
22 ? Pleurotus ostreatus pearl oyster Mycoterra Farm 2018-11-20 P-5 6AC1 🔬 🧬
23 ? Pleurotus tuber-regium king tuber 2019-09-21 P-2 EF1B 🔬 🧬
24 ? Stropharia rugoso-annulata garden giant · wine cap 2019-09-21 P-2 5547 🔬

todo: Freeze, revive, and fruit cultures on a convenient basis.

Future work

todo

An algorithm for the reasoning

if !funding
  unset nitrogen

  switch conditions
    water content
    temperature
    etc.

  foreach condition
    while nature modulo condition
    do mimic nature's conditions

else
  foreach cryo method
    consider [cost, ease, convenience]

freeze slow; thaw fast
return blog post

  1. OKAMURA, T., OGATA, T., MINAMOTO, N., TAKENO, T., NODA, H., FUKUDA, S., & OHSUGI, M. (2001). "Characteristics of Wine Produced by Mushroom Fermentation." Bioscience, Biotechnology, and Biochemistry, 65(7), 1596–1600. doi:10.1271/bbb.65.1596 ↩︎