Journal of Microbiology and Biotechnology

The Korean Society for Microbiology and Biotechnology (한국미생물·생명공학회)
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Inhibitory Effect of Hexane Fraction from Myagropsis myagroides on Pancreatic α-Amylase In Vitro

  • Pak, Won-Min (Department of Food Science and Technology/Institute of Food Science, Pukyong National University) ;
  • Kim, Koth-Bong-Woo Ri (Institute of Fisheries Sciences, Pukyong National University) ;
  • Kim, Min-ji (Institute of Fisheries Sciences, Pukyong National University) ;
  • Cho, Ji-Young (Department of Marine Biotechnology, Soonchunhyang University) ;
  • Ahn, Dong-Hyun (Department of Food Science and Technology/Institute of Food Science, Pukyong National University)
  • Received : 2014.09.04
  • Accepted : 2014.10.14
  • Published : 2015.03.28
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Abstract

A Myagropsis myagroides (Mm) methanol extract showed α-amylase inhibitory activity of 13% at a concentration of 5 mg/ml. Results showed that the hexane fraction from the Mm methanol extract exhibited α-amylase inhibitory activity with an IC50 value of 4.24 mg/ml. The hexane fraction was separated using silica-gel column chromatography, and six subfractions were obtained. The fraction eluted with CHCl3:MeOH = 50:1 showed the highest α-amylase inhibitory activity with an IC50 value of 0.72 mg/ml. This fraction was purified using Sephadex LH-20 column chromatography and an octadecyl silica (ODS) Sepak cartridge, obtaining seven subfractions. Fraction (Fr.) 4 also showed a strong α-amylase inhibitory activity with an IC50 value of 0.75 mg/ml. Fr. 4 was purified by Sephadex LH-20 column chromatography and ODS Sepak cartridge, obtaining six subfractions. Fr. 4-2 was identified as sargachromanol I with an IC50 value of 0.40 mg/ml, and the inhibition pattern analyzed from Lineweaver-Burk plots revealed it to be an uncompetitive inhibitor. These results suggest that Mm has potential as a natural antidiabetes agent.

Keywords

Introduction

α-Amylases (α-1,4-glucan-4-glucanohydrolase, E.C. 3.2.1.1) catalyze the hydrolysis of α-D-(1,4) glycosidic linkages in starch and glycogen [7,29]. α-Amylases (α-1,4-glucan-4-glucanohydrolase, E.C. 3.2.1.1) are widely distributed in plants, mammal tissues, and microorganisms. Starch is hydrolyzed into glucose by α-amylase in the intestine and maltase in the small intestine, which is more easily absorbed in the body as carbon and energy sources [7,15]. However, elevated amylase may cause high blood sugar and insulin levels, leading to diabetes, obesity, and acidosis [23,24]. Inhibitors of α-amylase affect the α-amylase kinetics of glucose absorption and blood glucose distribution by slowing the rate of starch digestion, resulting in an increase in the effect of dietary treatment of patients with diabetes mellitus or obesity due to a disorder of carbohydrate metabolism [21,22].

Acarbose is a well-known α-amylase inhibitor with potent α-amylase inhibitory activity. However, acarbose has undesirable side effects, especially flatulence and diarrhea, and its safety has become questionable [22]. Therefore, researchers are seeking α-amylase inhibitors from natural products that have fewer side effects. An α-amylase inhibitor isolated from buckwheat was first reported by Chrzaszcz and Janicki [5]. Other researchers have also reported αamylase inhibitors from terrestrial plants such as wheat [11], walnut [33], rye [8], and the bacterial strains Streptomyces sp. [10,25-28], Cladosporium sp. [32], and Actinoplanes sp.[32]. However, there are few studies on α-amylase inhibitors isolated from seaweeds. Some α-amylase inhibitors isolated from Ishige okamurae [12], Ecklonia cava [20], and Eisenia bicyclis [4] have been reported.

The brown seaweed, Myagropsis myagroides, belongs to the family Sargassaceae in Phaeophyta and most commonly inhabits the southern Korea and Japan coastlines. Studies on M. myagroides have mostly been focused on its antiinflammatory [18], antihypertensive [3], and anticoagulant activities [2], and protective effect on liver damage [34]. Despite abundant investigation, to date, there is no research on the α-amylase inhibitory effect of M. myagroides. Therefore, the aim of this study was to investigate the α-amylase inhibitory activity of M. myagroides extracts and isolate the active compound responsible for this effect.

 

Materials and Methods

Materials

M. myagroides was collected from the subtidal zone at Song-Jung, Busan, Korea. The samples were washed with tap water, lyophilized, and pulverized. The powder was stored at -20℃. Porcine pancreatic amylase (E.C. 3.2.1.1, type VI) and potato starch (type IV) were purchased from Sigma Co. (St. Louis, MO, USA).

Extraction

The dried M. myagroides (1.5 kg) was extracted three times with methanol for 24 h at room temperature. The extracts were filtered, centrifuged, and concentrated using a rotary evaporator (RE 200; Yamato Co., Tokyo, Japan) at 37℃. The dried methanol extract was stored at -20℃ until use.

Isolation of Sargachromanol I

The methanol extract was suspended in distilled water and partitioned successively with hexane, chloroform, ethyl acetate, and butanol. The hexane fraction (13 g) was separated by flash silica gel column chromatography (70–230 mesh; Merck Art, Darmstadt, Germany; 5 × 10 cm column, CHCl3:MeOH, 100:1-1:1 (v/v)). The fraction eluted with CHCl3:MeOH (50:1) was subjected to Sephadex LH-20 column chromatography (Amersham Pharmacia Biotech AB, Uppsala, Sweden; 2.5 × 90 cm column, CHCl3:MeOH, 1:1) and two fractions were separated on silica gel thin-layer chromatography (TLC; No. 5744, Merck; Darmstadt, Germany) plates with hexane-ethylacetate (2:1 (v/v)). Fr. 2 was subjected to octadecyl silica (ODS) Sepak cartridge (SPE C18 10 g; Grace, IL, USA; 60-90% methanol) and five fractions (Fr. 3 to Fr. 7) were isolated. Fr. 4 was successively subjected to Sephadex LH-20 column chromatography (methanol) and an ODS Sepak cartridge (50-60% methanol). The six fractions (Fr. 4-1-Fr. 4-6) were separated using ODS high-performance liquid chromatography (HPLC; ODS column i.d. 4.6 × 150 mm, 50-100% aqueous methanol gradient, 1 ml/min) and the fraction 4-2 was isolated using preparative HPLC (Cosmosil 5C18-MS II, 10 × 150 mm column; Nacalai Tesque, Kyoto, Japan; 70% aqueous methanol, 9 ml/min) and found to be a compound, sargachromanol I.

Sargachromanol I: 1H NMR (600 MHz, CDCl3) 6.37 (1H, d, 1.4 Hz), 5.27 (1H, s), 6.47 (1H, d, 2.8 Hz), 5.11 (1H, br t, 6.5 Hz), 4.87 (1H, dd, 9.7, 3.4 Hz), 3.91 (1H, d, 3.4 Hz), 4.97 (1H, br d, 9.6 Hz); 13C NMR (150 MHz, CDCl3) 75, 31.3, 22.4, 121.1, 112.6, 147.9, 115.6, 127.1, 39.5, 22.1, 124.8, 134.3, 39.4, 25.2, 33.4, 41.2, 214.6, 74.3, 120.9, 140, 25.9, 18.6, 16, 15.6, 24, 16.

α-Amylase Inhibitory Activity

The α-amylase inhibitory activity was measured following the method of Ali et al. [1] with a slight modification. Diluted samples (40 µl) and porcine pancreatic amylase (200 µl, 16 unit/ml) were added into test tubes and incubated at 25℃ for 5 min. A volume of 400 µl of 0.5% potato starch was added to the mixture for 3 min. Subsequently, 200 µl of this reactant and 100 µl of 96 mM DNS (potassium sodium tartrate in 2M NaOH) were mixed for 15 min at 85℃. The reaction was stopped by adding ultra pure water (900 µl) and the absorbance was measured at 540 nm using a UV/visible spectrophotometer (GENESYS 10 UV; Rochester, NY, USA). Acarbose (Sigma Co.) was used as a positive control and the inhibitory activity was calculated according to the formula given below, and the IC50 value (the concentration of the extract that results in 50% inhibition of maximal activity) was determined.

Inhibitory activity (%) = 100 - [(enzyme activity of test/enzyme activity of control)]

Kinetics of Inhibition

The inhibition was measured using increasing concentrations of starch as a substrate (5, 8, and 10 mM) in the presence of different concentrations (0, 0.8, and 1 mM) of sargachromanol I. The type of inhibition was determined using Lineweaver−Burk plot analysis of the data that were calculated from the results according to Michaelis−Menten kinetics.

 

Results and Discussion

α-Amylase Inhibitory Activity of M. myagroides Extracts

As shown in Table 1, the methanolic extract had a lower inhibitory activity (13%) at 5 mg/ml than acarbose. The methanolic extract was fractionated with n-hexane, chloroform, ethyl acetate, butanol, and water. The inhibitory effects of the fractions were higher than those of the methanolic extract in the order of chloroform > hexane > ethyl acetate, with IC50 values of 2.79, 4.24, and 4.28 mg/ml, respectively. However, all fractions were weaker than the positive control acarbose. The chloroform fraction showed the highest inhibition of α-amylase among the fractions, and this fraction was subjected to successive silica gel column chromatography. However, the most active subfraction obtained was not further analyzed owing to a low yield. Thus, the hexane fraction was selected for use in further experiments.

Table 1.-: less than 5%. =: Not done.

Table 2.-: less than 5%. =: Not done.

Table 3.-: less than 5%. =: Not done.

Table 4.-: less than 5%. =: Not done.

Table 5.α-Amylase inhibitory activity of subfractions (CM = 50:1) from the hexane fraction of Myagropsis myagroides methanol extract by HPLC.

α-Amylase Inhibitory Activity of Sargachromanol I

The hexane fraction was eluted with a chloroform/methanol mixture (100:1, 50:1, 20:1, 5:1, 1:1) using silica gel column chromatography. The fraction eluted from the chloroform/methanol mixture (50:1) exhibited the highest α-amylase inhibition, with an IC50 value of 0.72 mg/ml. The α-amylase inhibitory activity was higher than that of the positive control acarbose. The fraction eluted with the 50:1 chloroform/methanol mixture was submitted to a Sephadex LH-20 column with elution of a chloroform/methanol mixture, and to silica gel TLC with elution of a hexane/ethyl acetate mixture (2:1). Two fractions (Fr. 1 and Fr. 2) were obtained and Fr. 2 was subjected to an ODS Sepak cartridge with elution of 60−90% methanol. Five fractions (Fr. 3−Fr. 7) were obtained and Fr. 4 showed the highest α-amylase inhibitory actifvity, with an IC50 value of 0.75 mg/ml. Fr. 4 was purified using HPLC and six subfractions were obtained. Although Fr. 4-4 to Fr. 4-6 appeared to have potent α-amylase inhibitory activity, structural identification of these fractions was not possible owing to insufficient purity and amounts. The structures of Fr. 4-1 and Fr. 4-3 were also identified and their inhibitory activities will be presented in other papers. The sargachromanol I obtained from the Fr. 4-2 subfraction by preparative HPLC had a molecular mass of 428 Da. Sargachromanol I, with an IC50 value of 0.93 mM, showed a more potent inhibitory activity against α-amylase than that of the acarbose.

Meroterpenoids of the chromene class, consisting of a polyprenyl chain attached to a hydroquinone or similar aromatic rings, are widely distributed among marine organisms. Among the meroterpenoids, sargachromanols have been reported to possess several biological activities, including anticancer [13], antioxidant [17], and antiinflammatory [35] effects. Sargachromanol I was isolated from brown seaweed Sargassum siliquastrum [14] and its structure was similar to that of sargachromanol G [9]. To date, the biological activities of sargachromanol I on Na+/K+ ATPase inhibitory activity [6] and antioxidant activity [16] have been reported. Thus, to the best of our knowledge, this is the first report on its α-amylase inhibitory activity and isolation from M. myagroides. Sargachromanol I showed stronger inhibition against α-amylase than acarbose and may be an important contributor to the treatment of diabetes with α-amylase inhibitors.

Mode of α-Amylase Inhibition Type

The mode of inhibition of sargachromanol I on α-amylase was determined using the Lineweaver−Burk plot. Sargachromanol I displayed uncompetitive inhibition of the enzyme’s activity (Fig. 3). In this case, the inhibitor only binds to the enzyme-substrate complex but not the free enzyme. This plot suggests that sargachromanol I does not compete with the substrate for binding to the active site of the enzyme. Ponnusamy et al. [30] reported that bisdemethoxycurcumin isolated from the Curcuma longa rhizome showed uncompetitive inhibition against human pancreatic amylase. Lee and Lee [19] also reported that Chinese quince extract exhibited an uncompetitive inhibition mode.

Fig. 1.Solvent fractionation of the Myagropsis myagroides extract.

Fig. 2.HPLC profile of sargachromanol I isolated from Myagropsis myagroides methanol extract.

Fig. 3.Lineweaver-Burk plot for the inhibition of α-amylase by sargachromanol I. Variable dextrin from starch concentrations (5, 8, 10 mM) at fixed concentrations of sargachromanol I [0 mM (●), 0.8 mM ( ▲ ) and 1 mM (○)].

References

  1. Ali H, Houghon PJ, Soumyanath A. 2006. α-Amylase inhibitory activity of some Malaysian plants used to treat diabetes; with particular reference to Phyllanthus amarus. J. Ethnopharmacol. 107: 449-455. https://doi.org/10.1016/j.jep.2006.04.004
  2. Athukorala Y, Lee KW, Kim SK, Jeon YJ. 2007. Anticoagulant activity of marine green and brown algae collected from Jeju island in Korea. Bioresour. Technol. 98: 1711-1716. https://doi.org/10.1016/j.biortech.2006.07.034
  3. Cha SH, Ahn GN, Heo SJ, Kim KN, Lee KW, Song CB, et al. 2006. Screening of extracts from marine green and brown algae in Jeju for potential marine angiotensin-I converting enzyme (ACE) inhibitory activity. J. Korean Soc. Food Sci. Nutr. 35: 307-314. https://doi.org/10.3746/jkfn.2006.35.1.068
  4. Cho SH, Park SY, Choi SW. 2008. Effects of Eisenia bicyclis extracts and pill on blood glucose and lipid profile in streptozotocin-induced diabetic mice. Korean J. Nutr. 41: 493-501.
  5. Chrzaszcz T, Janicki J. 1933. “Sisto-amylase”, a natural inhibitor of amylase. Biochem. Z. 260: 354-368.
  6. Chung SC, Jang KH, Park J, Ahn CH, Shin J, Oh KB. 2011. Sargachromanols as inhibitors of Na+/K+ ATPase and isocitrate lyase. Bioorg. Med. Chem. Lett. 21: 1958-1961. https://doi.org/10.1016/j.bmcl.2011.02.035
  7. de Souza PM, de Oliveira Magalhães P. 2010. Application of microbial α-amylase in industry - a review. Braz. J. Microbiol. 41: 850-861. https://doi.org/10.1590/S1517-83822010000400004
  8. Dias SC, Franco OL, Magalhães CP, de Oliveira-Neto OB, Laumann RA, Figueira EL, et al. 2005. Molecular cloning and expression of an α-amylase inhibitor from rye with potential for controlling insect pests. Protein J. 24: 113-123. https://doi.org/10.1007/s10930-004-1518-4
  9. Dixon M. 1953. The determination of enzyme inhibitor constants. Biochem. J. 55: 170-171. https://doi.org/10.1042/bj0550170
  10. Fukuhara K, Murai H, Murso S. 1982. Amylostarins, other amylase inhibitors produced by Streptomyces diastaticus subsp. amylostaticus No. 2476. Agric. Biol. Chem. 46: 2021-2030. https://doi.org/10.1271/bbb1961.46.2021
  11. Granum PE. 1978. Purification and characterization of an amylase inhibitor from rye (Secale cerale) flour. J. Food Biochem. 2: 103-120. https://doi.org/10.1111/j.1745-4514.1978.tb00607.x
  12. Heo SJ, Hwang JY, Choi JI, Han JS, Kim HJ, Jeon YJ. 2009. Diphlorethohydroxy carmalol isolated from Ishige okamurae, a brown algae, a potent α-glucosidase and α-amylase inhibitor, alleviates postprandial hyperglycemia in diabetic mice. Eur. J. Pharmacol. 615: 252-256. https://doi.org/10.1016/j.ejphar.2009.05.017
  13. Heo SJ, Kim KN, Yoon WJ, Oh C, Choi YU, Affan A, et al. 2011. Chromene induces apoptosis via caspase-3 activation in human leukemia HL-60 cells. Food Chem. Toxicol. 49: 1998-2004. https://doi.org/10.1016/j.fct.2011.05.011
  14. Jang KH, Lee BH, Choi BW, Lee HS, Shin JH. 2005. Chromenes from the brown alga Sargassum siliquastrum. J. Nat. Prod. 68: 716-723. https://doi.org/10.1021/np058003i
  15. Jones BJM, Brown BE, Loran J, Edgerton D, Kennedy JF, Stead JA, Silk DBA. 1983. Glucose absorption from starch hydrolysates in the human jejunum. Gut 24: 1152-1160. https://doi.org/10.1136/gut.24.12.1152
  16. Kim EK. 2011. Studies on the bioactive compounds from Sargassum siliquastrum. MS thesis, Hanbat National University.
  17. Kim JA, Kong CS, Kim SK. 2010. Effect of Sargassum thunbergii on ROS mediated oxidative damage and identification of polyunsaturated fatty acid components. Food Chem. Toxicol. 48: 1243-1249. https://doi.org/10.1016/j.fct.2010.02.017
  18. Lee CJ, Song EJ, Kim KBWR, Jung JY, Kwak JH, Choi MK, et al. 2011. Effect of gamma irradiation on immune activity and physicochemical properties of Myagropsis myagroides water extract. Kor. J. Fish. Aquat. Sci. 4: 50-57.
  19. Lee JH, Lee SR. 1994. Some physiological activity of phenolic substance in plant foods.Korean J. Food Sci. Technol. 26: 317-323.
  20. Lee SH, Li Y, Karadeniz F, Kim MM, Kim SK. 2009. α-Glucosidase and α-amylase inhibitory activities of phloroglucinol derivatives from edible marine brown alga, Ecklonia cava. J. Sci. Food Agric. 89: 1552-1558. https://doi.org/10.1002/jsfa.3623
  21. Lee SJ, Song EJ, Kim KBWR, Lee CJ, Jung JY, Kwak JH, et al. 2010. Inhibitory effects of Sargassum thunbergii ethanol extract against α-amylase.Kor. J. Fish. Aquat. Sci. 43: 648-653.
  22. Lim CS. 2002. The inhibit ion of α-amylase and the antidiabetic effect in mouse by Cornus walteri extract. MS thesis, Kangwon National University.
  23. McLaughlin CL, Thompson A, Greenwood K, Sherington J, Bruce C. 2009. Effect of acarbose on acute acidosis. J. Dairy Sci. 92: 2758-2766. https://doi.org/10.3168/jds.2008-1602
  24. Menakshi B, Smita SZ, Shobha YB, Ameeta RK, Bimba NJ. 2011. Antidiabetic Indian plants: a good source of potent amylase inhibitors. Evid. Based Compl. Alt. Med. 2011: 1-6.
  25. Murao S, Goto A, Matsui Y, Ohyama K. 1981. New proteinous inhibitor (Haim) of animal α-amylase from Streptomyces griceosporeus YM-25. Agric. Biol. Chem. 44: 1679-1681. https://doi.org/10.1271/bbb1961.44.1679
  26. Murao S, Ohyama K. 1979. Chemical structure of an amylase inhibitor, S-AI. Agric. Biol. Chem. 43: 679-681. https://doi.org/10.1271/bbb1961.43.679
  27. Murao S, Oouchi N, Goto A, Arai M. 1983. New proteinous α-amylase inhibitor (Paim) from Streptomyces corchorushii. Agric. Biol. Chem. 47: 453-454. https://doi.org/10.1271/bbb1961.47.453
  28. Niwa T, Inouye S, Tsuruoka, T, Koaze Y, Niida T. 1970. Nojirimycin as a potent inhibitor of glucosidase. Agric. Biol. Chem. 34: 966-968. https://doi.org/10.1271/bbb1961.34.966
  29. Pallavi T, Leila LL, Johanna M, Renate UH, Arvind MK. 2007. α-Amylase from mung beans (Vigna radiata) – correlation of biochemical properties and tertiary structure by homology modeling. Phytochemistry 68: 1623-1631. https://doi.org/10.1016/j.phytochem.2007.04.006
  30. Ponnusamy S, Zinjarde S, Bhargava S, Rajamohanan PR, RaviKumar A. 2012. Discovering bisdemethoxycurcumin from Curcuma longa rhizome as a potent small molecule inhibitor of human pancreatic a-amylase, a target for type-2 diabetes. Food Chem. 135: 2638-2642. https://doi.org/10.1016/j.foodchem.2012.06.110
  31. Schmidt DD, Frommer W, Junge B, Müller L, Wingender W, Truscheit E, Schafer D. 1977. α-Glucosidase inhibitors new complex oligosaccharides of microbial origin. Naturwissenschaften 64: 535-536. https://doi.org/10.1007/BF00483561
  32. Saito N. 1982. α-Amylase inhibitor from fungus Cladosporium herbarum F-828. J. Biol. Chem. 257: 3120-3125.
  33. Skadsen RW. 1993. Aleurones from a barley with low [α]-amylase activity become highly responsive to gibberellin when detached from the starchy endosperm. Plant Physiol. 102: 195-203. https://doi.org/10.1104/pp.102.1.195
  34. Wong CK, Ooi VEC, Ang Jr PO. 2004. Hepatoprotective effect of seaweeds’ methanol extract against carbon tetrachlorideinduced poisoning in rats. Hydrobiologia 512: 267-270. https://doi.org/10.1023/B:HYDR.0000020336.06047.ac
  35. Yoon WJ, Heo SJ, Han SC, Lee HJ, Kang GJ, Kang HK, et al. 2012. Anti-inflammatory effect of sargachromanol G isolated from Sargassum siliquastrum in RAW 264.7 cells. Arch. Pharm. Res. 35: 1421-1430. https://doi.org/10.1007/s12272-012-0812-5

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