Materials and Reagents

Aspergillus nidulans conidia
Trisodium citrate dihydrate (C₆H₅Na₃O₇^.2H₂O) (Wako Pure Chemical Industries, catalog number: 191-01785 )
Citric acid (C₆H₈O₇) (Wako Pure Chemical Industries, catalog number: 030-05525 )
Ethyl-4-aminobenzoate (C₉H₁₁NO₂) (ABEE) (Tokyo Chemical Industry, catalog number: A0271 )
Sodium cyanoborohydride (NaBH₃CN) (Tokyo Chemical Industry, catalog number: S0396 )
Chloroform (Wako Pure Chemical Industries, catalog number: 038-02606 )
Ethanol (Wako Pure Chemical Industries, catalog number: 050-00446 )
Trifluoroacetic acid (TFA) (Wako Pure Chemical Industries, catalog number: 206-10731 )
Glacial acetic acid (Wako Pure Chemical Industries, catalog number: 012-00245 )
Methanol (Wako Pure Chemical Industries, catalog number: 136-09475 )
D-galactose (Sigma-Aldrich, catalog number: G0750 )
ABEE labeling mixture (see Recipes)
HPLC solvent A (see Recipes)
HPLC solvent B (see Recipes)
Minimal medium (see Recipes)
Hutner's trace elements (see Recipes)

Equipment

50-ml plastic centrifuge tube (e.g., Greiner Bio-One GmbH)
1.5-ml conical screw cap tube and cap
Spreader
500-ml Sakaguchi flasks
Centrifuge
Rotator (e.g., TAITEC)
High-performance liquid chromatography (HPLC) system equipped with a fluorescence detector (Hitachi, LaChrom Elite, model: L-2485) and software for HPLC peak analysis (e.g., Hitachi, model: D-2000 Elite HPLC)
Centrifugal evaporator (e.g., SpeedVac^®)
Heat block or water bath
GlycoScope Honenpak C18 column (4.6 mm x 75 mm) (COSMO BIO, catalog number: JOM-J715-1PC)
Filter paper (Munktell & Filtrak GmbH, catalog number: 113053 )
Dialysis membrane (BioDesign Inc. of New York, catalog number: D102 )

Procedure

Streak Aspergillus nidulans conidia from frozen stock onto Minimal medium (MM) plate and cultivate for 3 days at 30 °C.
Collect the formed conidia with a spreader.
Spread Aspergillus nidulans conidia (1 x 10⁵) onto MM plates and cultivate for 3 days at 30 °C.
Inoculate the collected conidia (2 x 10⁷) into 100 ml of MM in 500-ml Sakaguchi flasks.
Shake the flasks at 126 rpm at 30 °C for 24 h.
Collect the mycelial cells by paper filtration.
Wash the cells twice with approximately 30 ml of distilled water (Video 1).

Video 1. Collection and washing of the mycelial cells
Resuspend the cells (approx. 2 g of wet cells) in 10 ml of 100 mM citrate buffer (pH 7.0).
Autoclave the sample at 121 °C for 120 min.
Remove cell debris by paper filtration (Video 2).

Video 2. Removing cell debris by paper filtration
Collect the resultant sample (approx. 10 ml) in a 50-ml plastic centrifuge tube.
Add 30 ml of cold 99.5% ethanol and keep the sample on ice for 30 min.
Centrifuge at 14,000 x g at 4 °C for 10 min.
Dry the pellet at room temperature using a centrifugal evaporator at 1,500 x g.
Resuspend the pellet in 2 ml of distilled H₂O (dH₂O).
Dialyze the sample with a dialysis membrane (15.5 mm x 300 mm) against 5 L of dH₂O for 24 h at 4 °C. The resultant sample is designated as the extracted galactomannnoproteins.
Incubate part (2.4 µg) of the extracted galactomannoproteins in 500 µl of 4 M trifluoroacetic acid (TFA) at 100 °C for 4 h in a 1.5-ml conical screw cap tube.
Dry the resultant sample at room temperature using a centrifugal evaporator at 1,500 x g.
Resuspend the sample in 10 µl of dH₂O.
Label the hydrolysates with fluorescent p-aminobenzoic acid ethyl ester (ABEE) using an ABEE labeling mixture.
1. Add 40 µl of the ABEE labeling mixture (preheating at 70 °C for 5 min) to the sample.
2. Incubate the sample for 1 h at 80 °C.
3. Cool the sample to room temperature.
4. Add 200 µl of dH₂O and 200 µl of chloroform to the sample.
5. Vigorously vortex the sample and then centrifuge it at 14,000 x g for 5 min at room temperature.
6. Collect the upper aqueous layer.
Analyze the ABEE-labeled D-galactopyranose using an HPLC system. Inject 20 µl of the sample into the column at a flow rate of 1.0 ml/min at 45 °C. ABEE-D-galactopyranose can be detected with a fluorescence detector at an excitation wavelength of 360 nm and an emission wavelength of 305 nm.
Note: Use solvents containing acetonitrile and potassium borate buffer (see the Recipes section for solvents A and B). Set the gradient program at a flow rate of 1.0 ml/min (expressed as a percent of solvent A) and apply the following gradient to analyze the ABEE-D-galactopyranose: 0-45 min, isocratic 100%; 45-50 min, 100-0%; 50-55 min, 0-100%; 55-75 min, isocratic 100%. Use D-galactose as a standard for quantification purposes.

Recipes

ABEE labeling mixture
165 mg ABEE
35 mg sodium cyanoborohydride
41 µl glacial acetic acid
350 µl methanol
The mixture can be long-term stored at -20 °C
HPLC solvent A [0.2 M potassium borate buffer (pH 9.0) containing 6% acetonitrile]
12.4 g H₃BO₃
60 ml acetonitrile
Add water to bring the final solution to 1 L total volume while adjusting pH 9.0 with potassium hydroxide (KOH)
HPLC solvent B [0.2 M potassium borate buffer (pH 9.0) containing 50% acetonitrile]
12.4 g H₃BO₃
500 ml acetonitrile
Add water to bring the final solution to 1 L total volume while adjusting pH 9.0 with potassium hydroxide (KOH)
Minimal medium (1 L)
NaNO₃
6.0 g
KCl
0.52 g
KH₂PO₄
1.52 g
Glucose
10.0 g
Hutner's trace elements
2 ml
Adjust the pH value to 6.8 using NaOH
Add water to bring the final solution to 1 L total volume
Autoclave for 20 min
Hutner's trace elements
H₂O (60 ˚C)
100 ml
ZnSO₄•7H₂O
2.2 g
H₃BO₃
1.1 g
MnCl₂•4H₂O
0.5 g
FeSO₄•7H₂O
0.5 g
CoCl₂•6H₂O
0.16 g
CuSO₄•5H₂O
0.16 g
(NH₄) 6Mo₇O₂₄•4H₂O
0.11 g
EDTA
5.0 g
Adjust the pH value to 6.5-6.8 using KOH

Acknowledgments

This protocol was adapted from the previously published papers Komachi et al. (2013) and Yasuno et al. (1997). The work was supported in part by Grants-in-Aid for Young Scientists (B) from the Japan Society of the Promotion of Science (JSPS) (21780313, 23780350 and 26450106) (to T.O.).

References

Komachi, Y., Hatakeyama, S., Motomatsu, H., Futagami, T., Kizjakina, K., Sobrado, P., Ekino, K., Takegawa, K., Goto, M., Nomura, Y. and Oka, T. (2013). GfsA encodes a novel galactofuranosyltransferase involved in biosynthesis of galactofuranose antigen of O-glycan in Aspergillus nidulans and Aspergillus fumigatus. Mol Microbiol 90(5): 1054-1073.
Yasuno, S., Murata, T., Kokubo, K., Yamaguchi, T. and Kamei, M. (1997). Two-mode analysis by high-performance liquid chromatography of ρ-aminobenzoic ethyl ester-derivatized monosaccharides. Biosci Biotec Biochem 61(11): 1944-1946.