Patatin, the Tuber Storage Protein of Potato (Solanum
tuberosum L.), Exhibits Antioxidant Activity in Vitro
YEN-WENN
LIU,
†,§CHUAN-HSIAO
HAN,
#,§MEI-HSIEN
LEE,
#FENG-LIN
HSU,*
,# ANDWEN-CHI
HOU*
,#School of Pharmacy and Graduate Institute of Pharmacognosy, Taipei Medical University, Taipei 110, Taiwan, Republic of China
The potato (Solanum tuberosum L.) tuber storage protein, patatin, was purified to homogeneity with a molecular mass of 45 kDa. The purified patatin showed antioxidant or antiradical activity by a series of in vitro tests, including 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical (half-inhibition concentration, IC50, was 0.582 mg/mL) scavenging activity assays, anti-human low-density lipoprotein peroxidation tests, and protections against hydroxyl radical-mediated DNA damages and peroxynitrite-mediated dihydrorhodamine 123 oxidations. Using electron paramagnetic resonance (EPR) spectrometry for hydroxyl radical detections, it was found that the intensities of the EPR signal were decreased by the increased amounts of patatin added (IC50was 0.775 mg/mL). Through modifications of patatin by iodoacetamide orN-bromosuccinimide, it was found that the antiradical activities of modified patatin against DPPH or hydroxyl radicals were decreased. It was suggested that cysteine and tryptophan residues in patatin might contribute to its antioxidant activities against radicals.
KEYWORDS: Antioxidant; 1,1-diphenyl-2-picrylhydrazyl (DPPH); electron paramagnetic resonance (EPR); hydroxyl radical;Solanum tuberosum; storage protein
INTRODUCTION
Active oxygen species (or reactive oxygen species) and free
radical-mediated reactions are involved in degenerative or
pathological processes such as aging (1), cancer, coronary heart
disease, and Alzheimer’s disease (2, 3). There are several reports
concerning natural compounds in fruits and vegetables with
regard to their antioxidant activities in vitro, including water
extracts of roasted Cassia tora (4), phenolic compounds (5),
the storage proteins of sweet potato root (6) and yam tuber (7),
and whey proteins (8, 9).
Patatin is the trivial name given to a family of glycoproteins
that make up >40% of the total soluble protein in potato
(Solanum tuberosum) tubers and serves as a storage protein. It
was proved that patatin exhibited both lipid acyl hydrolase and
acyltransferase activities, which might be involved in tuber tissue
in the response to wounding (10). Al-Saikhan et al. (11) showed
that different potato cultivars exhibited different antioxidant
activities, which were higher than those of bell pepper, carrot,
and onion. They found that different components in potato,
including chlorogenic acid (300
µg/mL), glutathione (100 µg/
mL), ascorbic acid (320
µg/mL), quercetin (15 µg/mL), and
patatin (33 mg/mL), had antioxidant activities against the
coupled oxidation of
β-carotene and linoleic acid. In this work
we report that purified patatin had different antioxidant activities
in comparison with chemicals such as butylated hydroxytoluene
(BHT) or reduced glutathione in a series of in vitro tests. We
also used chemicals for amino acid side-chain modifications to
identify key positions involved in the antioxidant activities of
patatin.
MATERIALS AND METHODS
Materials. Tris, 2-thiobarbituric acid (TBA), and electrophoretic reagents were purchased from E. Merck Inc. (Darmstadt, Germany). Peroxynitrite was obtained from Calbiochem-Novabiochem Co. (Darm-stadt, Germany). Calf thymus DNA (activated, 25 A260units/mL) was purchased from Amersham Biosciences (Uppsala, Sweden). Hydrogen peroxide (33%) was from Wako Pure Chemicals Industry (Osaka, Japan). BHT, reduced glutathione, dihydrorhodamine 123 (DHR), 1,1-diphenyl-2-picrylhydrazyl (DPPH), human low-density lipoprotein (LDL), iodoacetamide, N-bromosuccinimide (NBSI), phenylmethane-sulfonyl fluoride (PMSF), 2-deoxyribose, peroxynitrite, and other chemicals and reagents were purchased from Sigma Chemical Co. (St. Louis, MO).
Patatin Extractions and Purifications. Fresh potato (S. tuberosum) tubers were purchased from a wholesaler. After washing and peeling, the tubers were cut into strips for patatin extraction and purification. After extraction and centrifugation, patatins were purified from crude extracts successively by a DEAE-Sepharose CL-6B ion exchange column and a Con A affinity column according to the methods of Racusen and Foote (12). The eluted fraction was collected and concentrated with Ultrafree-4 (molecular weight cutoff is 5 kDa, Millipore Co., Bedford, MA). The concentrated patatin solution was * Authors to whom corrrespondence should be addressed at the Graduate
Institute of Pharmacognosy, Taipei Medical University, No. 250 Wu-Hsing Street, Taipei 110, Taiwan, ROC [fax 886 (2) 2378-0134; e-mail (W.-C.H.) [email protected] or (F.-L.H.) [email protected]].
†School of Pharmacy. §Equal contributions.
#Graduate Institute of Pharmacognosy.
J. Agric. Food Chem. 2003, 51, 4389
−
4393
4389
10.1021/jf030016j CCC: $25.00 © 2003 American Chemical Society Published on Web 06/17/2003
dialyzed against deionized water overnight and lyophilized for further use.
Protein Staining on SDS-PAGE Gels. Sixteen microliters of patatin solution was mixed with 4µL of sample buffer, namely, 60 mM
Tris-HCl buffer (pH 6.8) containing 2% SDS, 25% glycerol, and 0.1% bromophenol blue without 2-mercaptoethanol, and heated in boiling water for 5 min followed by electrophoresis according to the method of Laemmli (13). Coomassie brilliant blue R-250 was used for protein staining (14).
Scavenging Activity of DPPH Radical by Spectrophotometry. The scavenging activity of purified patatin against DPPH radical was measured according to the method of Hou et al. (6, 7, 15). Every 0.3 mL of patatin solution [from 0.1 mg/mL (2.22 nmol) to 0.7 mg/mL (15.54 nmol)] was added to 0.1 mL of 1 M Tris-HCl buffer (pH 7.9) and then mixed with 0.6 mL of 100µM DPPH in methanol to the
final concentrations of 60µM for 20 min under light protection at room
temperature. The absorbance at 517 nm was measured. Deionized water was used as blank experiment, and BHT [from 1µg/mL (4.54 nmol)
to 5µg/mL (22.7 nmol)] and reduced glutathione [from 1 µg/mL (3.25
nmol) to 12.5µg/mL (40.68 nmol)] were used as positive controls.
The scavenging activity of DPPH radicals (%) was calculated with the equation (A517,blank- A517,sample)÷ A517,blank× 100%. IC50identifies the concentration of half-inhibition.
Scavenging Activity of Hydroxyl Radicals by EPR Spectrometry. The hydroxyl radical was generated by Fenton reaction according to the method of Kohno et al. (16). The total 500-µL mixture included
45 kDa patatin (0.194, 0.388, 0.775, and 1.55 mg/mL), 5 mM 5,5-dimethyl-1-pyrroline-N-oxide (DMPO), and 0.05 mM ferrous sulfate. After mixing, the solution was transferred to an EPR quartz cell and placed at the cavity of the EPR spectrometer, and then hydrogen peroxide was added to a final concentration of 0.25 mM. Deionized water was used instead of sample solution for blank experiments. After 40 s, the relative intensity of the signal of the DMPO-OH spin adduct was measured. All EPR spectra were recorded at the ambient temper-ature (298 K) on a Bruker EMX-6/1 EPR spectrometer equipped with WIN-EPR SimFonia software version 1.2. The conditions of EPR spectrometry were as follows: center field, 345.4 ( 5.0 mT; microwave power, 8 mW (9.416 GHz); modulation amplitude, 5 G; modulation frequency, 100 kHz; time constant, 0.6 s; scan time, 1.5 min.
Modified Patatin against DPPH and Hydroxyl Radicals. The 250
µL of purified patatin (10 mg/mL) was modified by different chemicals
as follows. (1) The cysteine residues were alkylated by 10µL of 200
mM iodoacetamide to the final concentrations of 200µM (17) at Tris
buffer (pH 8.3), 37°C for 2 h, and then dialyzed against deionized water overnight. (2) The tryptophan residues were modified by 0.6 mL of 1 mM NBSI (18) in 0.1 M acetate buffer (pH 4.0) to the concentration of 150 µM at room temperature for 1 h and then dialyzed against
deionized water overnight. The purified patatin with or without chemical modifications was used for scavenging activity assays against DPPH and hydroxyl radicals described aboved.
Protection against Cu2+-Induced LDL Peroxidation by Patatin. The capacity of purified patatin (0.2-1.2 mg/mL) against Cu2+-induced human LDL oxidation in a total 1.1-mL sample volume was measured by thiobarbituric acid reactive substances (TBARS) assay at a wavelength of 532 nm (19). The LDL (0.5 mg of protein/mL) was incubated at 37 °C under air in 10 mM phosphate buffer (pH 7.4) containing 10µM CuSO4for 24 h with or without purified patatin. The peroxidation reaction was stopped by adding 100µM EDTA. The
TBARS value of 24-h LDL peroxidation was assumed as 100%. BHT was used as a positive control.
Protection against Hydroxyl Radical-Induced Calf Thymus DNA Damage by Patatin. The hydroxyl radical was generated by Fenton reaction according to the method of Kohno et al. (16). The 45-µL
reaction mixture included 45 kDa patatin (0.182, 0.364, 0.910, 1.82, and 3.64 mg/mL), 15µL of calf thymus DNA (25 A260units/mL), 18 mM FeSO4, and 60 mM hydroxygen peroxide at room temperature for 15 or 30 min. Then 10µL of 1 mM EDTA was added to stop the
reaction. Only calf thymus DNA was used for blank test, and the control test was without patatin additions. After agarose electrophoresis, the treated DNA solutions were stained with ethidium bromide and observed under UV light.
Protection against Peroxynitrite-Mediated DHR Oxidation by Patatin. The protection of peroxynitrite-mediated DHR oxidation was according to the methods of Kooy et al. (20). The total 180-µL reaction
mixture included different amounts of 45 kDa patatin (22.22, 55.56, 111.11, and 277.78µg/mL), 0.9 mM DHR, and 5 µL of peroxynitrite
in 50 mM phosphate buffer (pH 7.4) containing 90 mM NaCl. After 5 min of reaction, the fluorescent intensity was measured at the excitation and emission wavelengths of 500 and 536 nm, respectively, and excitation and emission slit widths of 2.5 and 3.0 nm, respectively. The control test was without patatin additions.
Statistics. Means of triplicates were measured. Student’s t test was used for comparison between two treatments. A difference was considered to be statistically significant when p < 0.05.
RESULTS AND DISCUSSION
Patatin Purification from Potato Tuber. The purity of
patatin was determined by an SDS-PAGE gel. Figure 1 showed
the protein stainings of patatin. A single band (lane 1) with a
molecular mass of 45 kDa was found. This result was the same
as that of Racusen and Foote (12). This purified patatin was
lyophilized for further investigations.
Antiradical Activity of Patatin on DPPH. The effects of
different concentrations of purified patatin or the nanomole basis
of purified patatin on the scavenging activities of DPPH radicals
with spectrophotometry are shown in Figure 2. BHT and
reduced glutathione were used as positive controls. It was found
that patatin exhibited dose-dependent scavenging activity against
DPPH radicals from 0.1 to 0.7 mg/mL for 12-61%,
respec-tively. The IC
50for DPPH radical scavenging activity was 0.582
mg/mL (Figure 2A). The anti-DPPH radical capacities of
purified patatin were about
1/
140
that of BHT or
1/
56that of
reduced glutathione; however, under the nanomole basis, the
anti-DPPH radical capacities of purified patatin were similar
to that of BHT and higher than that of reduced glutathione
(Figure 2B).
Scavenging Activity of Patatin against Hydroxyl Radical
Determined by EPR Spectrometry. The hydroxyl radical was
generated by Fenton reaction and was trapped by DMPO to
form the OH adduct. The intensities of the
DMPO-OH spin signal in EPR spectrometry were used to evaluate the
scavenging activity of 45 kDa potato patatin against hydroxyl
radical. Figure 3 shows the scavenging activity against the
hydroxyl radical with different amounts of 45 kDa patatin: (A)
blank, (B-E) 0.194, 0.388, 0.775, and 1.55 mg/mL, respectively,
purified patatin. The effect of 45 kDa patatin as a scavenger of
hydroxyl radical was evident as decreased intensities of
DMPO-OH signals. EPR signals were significantly decreased
Figure 1. Protein stainings of patatin on an SDS-PAGE gel after ion exchange column and Con A affinity purifications. M indicates the Seeblue prestained markers of SDS-PAGE. Two micrograms of protein was loaded in each well.by 0.194-1.55 mg/mL of 45 kDa patatin compared to the blank
with a positive correlation between two parameters (r ) 0.971).
On the basis of DMPO-OH signal intensities, there were about
23, 39, 50, and 69% reductions, respectively, by 0.194, 0.388,
0.775, and 1.55 mg/mL of patatin compared to controls (Figure
3B-E). The IC
50for hydroxyl radical scavenging activity was
0.775 mg/mL. Figure 3 provides the first piece of evidence
that potato patatin exhibited scavenging activity against hydroxyl
radical as shown by EPR spectrometry.
Scavenging Activity of Modified Patatin against DPPH
and Hydroxyl Radicals. Chemicals were used for amino acid
side-chain modifications to identify key positions involved in
antioxidant activities of patatin. From the results of Figure 4,
it was found that all modifications could apparently scavenge
activities against DPPH and hydroxyl radicals. Yan et al. (21)
reported that tryptophan exhibited anti-hydroxyl radical
activi-ties. Free cysteine residues in whey proteins (8, 9) were also
reported to have antioxidant activities. These findings mean that
cysteine and tryptophan residues in potato patatin participated
in the antiradical activities.
Effect of Purified Patatin on Protecting Cu
2+-Induced
Human LDL Peroxidation by TBARS Assay. LDL
peroxi-dation has been reported to contribute to atherosclerosis
development (22). Therefore, delay or prevention of LDL
peroxidation is an important function of antioxidants. With the
TBARS assay, the degrees of Cu
2+-induced human LDL
peroxidation could be revealed. From the results of Figure 5,
the protection effect of purified patatin against LDL peroxidation
was dose-dependent. The protection capacities of purified patatin
were 9, 9, 10, 22.5, 30, and 45% for 0.2, 0.4, 0.6, 0.8, 1.0, and
1.2 mg/mL, respectively. Significant difference was observed
among the oxidized LDL, oxidized LDL + 0.8 mg/mL purified
patatin (p < 0.05), and oxidized LDL + 1.0 mg/mL purified
patatin or 1.2 mg/mL purified patatin (p < 0.01).
Protecting Hydroxyl Radical-Induced Calf Thymus DNA
Damage by Patatin. Free radicals could damage
macromol-ecules in cells, such as DNA, protein, and lipids in membranes
(23). Figure 6 shows that purified patatin protected against
hydroxyl radical-induced calf thymus DNA damages. Only calf
thymus DNA was used for the blank test, and the control test
was without patatin additions. Compared to the blank test and
control test, it was found that the added patatin above 0.364
mg/mL could protect against hydroxyl radical induced calf
thymus DNA damages during 15-min (Figure 6A) or 30-min
(Figure 6B) reactions.
Protecting Peroxynitrite-Mediated DHR Oxidation by
Patatin. Peroxynitrite is formed from nearly diffusion limited
reaction between nitric oxide and superoxide and an initiator
of potentially harmful oxidation reaction (24). From the results
of Figure 7, it was found that the protective effect of
peroxynitrite-mediated DHR oxidation of purified patatin was
dose-dependent. The protection capacities of purified patatin
were 8.36, 32.78, 41.07, and 46.57% for 22.22, 55.56, 111.11,
and 277.78
µg/mL, respectively. Significant difference was
observed between the peroxnitrite, peroxnitrite + 22.22
µg/mL
purified patatin (p < 0.05), and peroxnitrite + 55.56
µg/mL
patatin or 111.11
µg/mL patatin or 277.78 µg/mL patatin (p <
0.01).
In conclusion, the results from in vitro experiments, including
DPPH radical (Figure 2) and hydroxyl radical (Figure 3)
scavenging activity assays, anti-human LDL oxidation analysis
(Figure 5), protection against hydroxyl radical-induced calf
Figure 2. Effects of different concentrations of (A) 0.1, 0.2, 0.3, 0.4,0.5, 0.6, and 0.7 mg/mL of purified patatin or (B) 2.22, 4.44, 6.66, 8.88, 11.1, 13.32, and 15.54 nmol of purified patatin on the scavenging activities of DPPH radicals with spectrophotometry. BHT [(A) 1, 1.25, 2.5, 3, 4, and 5 µg/mL corresponding to (B) 4.54, 5.67, 11.35, 13.62, 18.16, and 22.7 nmol, respectively] and reduced glutathione [(A) 1, 1.25, 2.5, 5, 10, and 12.5 µg/mL corresponding to (B) 3.25, 4.07, 8.14, 16.27, 32.54, and 40.68 nmol, respectively] were used as positive controls. The scavenging activity of DPPH radicals (%) was calculated with the following equation: (A517,blank−A517,sample)÷A517,blank×100%.
Figure 3. Scavenging activities of purified patatin against hydroxyl radicals by EPR spectrometry: (A) deionized water as a blank; (B) 0.194 mg/mL patatin; (C) 0.388 mg/mL patatin; (D) 0.775 mg/mL patatin; (E) 1.55 mg/mL patatin. The signal intensities of the DMPO-OH adduct were determined.
thymus DNA damage (Figure 6), and protection against
peroxynitrite-mediated DHR oxidadtion (Figure 7),
demon-strated that purified patatin exhibited antioxidant activities. It
was also demonstrated that cysteine and tryptophan residues in
patatin were involved in antiradical activity against DPPH and
hydroxyl radicals. Al-Saikhan et al. (11) reported that patatin
at 33 mg/mL exhibited an antioxidant activity that was very
similar to that in potato extracts. From the above experimental
results, it is revealed that 45 kDa patatin could capture radicals
in aconcentration-dependent manner and may play a role as an
antioxidant in potato tubers, which accounted for up 40% of
the total soluble proteins, and may be beneficial when it is
consumed for its nutritional and antioxidant activity. Some in
vivo experiments will need for further investigations.
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Figure 7. Purified patatin (22.22, 55.56, 111.11, and 277.78 µg/mL) protected against peroxynitrite-mediated dihydrorhodamine 123 oxidation. The total 180-µL reaction mixture included different amounts of purified patatin, 0.9 mM DHR, and 5 µL of peroxynitrite in 50 mM phosphate buffer (pH 7.4) containing 90 mM NaCl. After 5 min of reaction, the fluorescent intensity was measured. The control test was without patatin additions. A difference was considered to be statistically significant when p < 0.05 (*) or p < 0.01 (**).
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Received for review January 8, 2003. Accepted April 23, 2003. We thank the National Science Council, Republic of China, for financial support (NSC 91-2313-B-038-002).
