Open Access Open Access  Restricted Access Subscription Access

Identification of Bioactive Compound from Citrus maxima Fruit against Carbohydrate-Hydrolysing Enzymes


Affiliations
1 Department of Fruit and Vegetable Technology, CSIR-Central Food Technological Research Institute, Mysuru 570 020, India
2 Department of Food Protectants and Infestation Control, CSIR-Central Food Technological Research Institute, Mysuru 570 020, India
3 Department of Spices and Flavor Science, CSIR-Central Food Technological Research Institute, Mysuru 570 020, India
 

The aim of this study was to identify the bioactive compound of Citrus maxima fruit that targets the enzymes responsible for hyperglycaemia. Preliminary in vitro screening of extracts of fruit parts revealed that juicy segments (ethanol, methanol and aqueous) showed the highest inhibition towards the carbohydrate- hydrolysing enzymes. Further, juicy segment extracts were subjected to preparative HPLC for separation and isolation of compounds. After a series of separations, in vitro analysis and characterization, naringin was identified to be the bioactive compound that is responsible for inhibiting carbohydrate-hydrolysing enzyme activities. Further application, such as developing food formulations from C. maxima will benefit diabetic populations.

Keywords

Bioactive Compound, Citrus maxima, Carbohydrate- Hydrolysing Enzymes, Hyperglycaemia.
User
Notifications
Font Size

  • Bhandurge, P., Rajarajeshwari, N., Alagawadi, K. R. and Agrawal, S., Antidiabetic and hyperlipaemic effects of Citrus maxima Linn. fruits on alloxan-induced diabetic rats. Int. J. Drug Dev. Res., 2010, 2, 273–278.
  • Mangesh, K., Vidyasagar, G. and Ashwini, K., Antidiabetic potential of ethanolic extracts of Citrus maxima fruit peel and Anvillea garcinii. Int. J. Pharm. Innov., 2014, 4, 8–18.
  • Makynen, K. et al., Cultivar variations in antioxidant and antihyperlipidemic properties of pomelo pulp (Citrus grandis [L.] Osbeck) in Thailand. Food Chem., 2013, 139, 735–745.
  • Shivananda, A., Muralidhara, R. D. and Jayaveera, K. N., Analgesic and anti-inflammatory activities of Citrus maxima (J. Burm) Merr. in animal models. Res. J. Pharm. Biol. Chem. Sci., 2013, 4, 1800–1810.
  • Abdul, M. M. T., Shenoy, A., Hegde, K., Aamer, S. and Shabaraya, A. R., Evaluation of the anti-diabetic activity of ethanolic extract of Citrus maxima stem bark. Int. J. Pharm. Chem. Sci., 2014, 3, 642–650.
  • Caengprasath, N., Ngamukote, S., Makynen, K. and Adisakwattana, S., The protective effects of pomelo extract (Citrus grandis L. Osbeck) against fructose-mediated protein oxidation and glycation. EXCLI J., 2013, 12, 491–502.
  • Ding, X., Guo, L., Zhang, Y., Fan, S., Gu, M., Lu, Y. and Zhou, Z., Extracts of pomelo peels prevent high-fat diet-induced metabolic disorders in c57bl/6 mice through activating the PPARα and GLUT4 pathway. PLOS ONE, 2013, 8, e77915.
  • Kundusen, S., Gupta, M., Upal, K. M., Pallab, K. H., Prerona, S. and Asis, B., Antitumor activity of Citrus maxima (Burm.) Merr. leaves in Ehrlichascites carcinoma cell-treated mice. ISRN Pharmacol., 2011, 2011, 1–4.
  • Merina, N., Chandra, K. J. and Jibon, K., Medicinal plants with potential anticancer activity: review. Int. Res. J. Pharm., 2012, 3, 26–30.
  • Cheong, M. W., Liu, S. Q., Zhou, W., Curran, P. and Yu, B., Chemical composition and sensory profile of pomelo (Citrus grandis (L.) Osbeck) juice. Food Chem., 2012, 135, 2505–2513.
  • Russo, M., Bonaccorsia, I., Torrea, G., Cotroneoa, A., Dugoa, P. and Luigi, M. Determination of bioactive compounds in the juice of pummelo (Citrus grandis Osbeck). Nat. Prod. Commun., 2013, 8, 171–174.
  • Duan, L., Guo, L., Li-Li, D., Ke-Yun, Y., E-Hu, L. and Ping, L., Comparison of chemical profiling and antioxidant activities of fruits, leaves, branches and flowers of Citrus grandis ‘Tomentosa’. J. Agric. Food Chem., 2014, 62, 11122−11129.
  • Zhang, M., Haijuan, N., Yanjie, W., Xiaoying, J. and Zheng, L., Comparison of flavonoid compounds in the flavedo and juice of two pummelo cultivars (Citrus grandis L. Osbeck) from different cultivation regions in China. Molecules, 2014, 19, 17314–17328.
  • Kim, Y. M., Jeong, Y. K., Wang, M. H., Lee, Y. H. and Rhee, H. I., Inhibitory effect of pine extract on alpha-glucosidase activity and postprandial hyperglycaemia. Nutrition, 2005, 21, 756–761.
  • Kazeem, M. I., Raimi, O. G., Balogun, R. M. and Ogundajo, A. L., Comparative study on the α-amylase and α-glucosidase inhibitory potential of different extracts of Blighia sapida Koenig. Am. J. Res. Commun., 2013, 1, 178–192.
  • Eynard, L., Guerrieri, N. and Cerletti, G., Modifications of starch during baking: studied through reactivity with amyloglucosidase. Cereal Chem., 1995, 72, 594–597.
  • Pinto, M. D., Kwon, Y., Apostolidis, E., Lajolo, F. M., Genovese, M. I. and Shetty, K., Potential of Ginkgo biloba L. leaves in the management of hyperglycemia and hypertension using in vitro models. Bioresour. Technol., 2009, 100, 6599–6609.
  • Oboh, G. and Ademosun, A. O., Shaddock peels (Citrus maxima) phenolic extracts inhibit α-amylase, α-glucosidase and angiotensin I-converting enzyme activities: a nutraceutical approach to diabetes management. Diabetes Metab. Syndr., 2011, 5, 48–52.
  • Ma, X., Chen, Z., Chen, R., Zheng, X., Chena, X. and Lan, R., Imprinted β-cyclodextrin polymers using naringin as template. Polym. Int., 2011, 60, 1455–1460.

Abstract Views: 476

PDF Views: 105




  • Identification of Bioactive Compound from Citrus maxima Fruit against Carbohydrate-Hydrolysing Enzymes

Abstract Views: 476  |  PDF Views: 105

Authors

S. K. Reshmi
Department of Fruit and Vegetable Technology, CSIR-Central Food Technological Research Institute, Mysuru 570 020, India
H. K. Manonmani
Department of Food Protectants and Infestation Control, CSIR-Central Food Technological Research Institute, Mysuru 570 020, India
J. R. Manjunatha
Department of Spices and Flavor Science, CSIR-Central Food Technological Research Institute, Mysuru 570 020, India
M. N. Shashirekha
Department of Fruit and Vegetable Technology, CSIR-Central Food Technological Research Institute, Mysuru 570 020, India

Abstract


The aim of this study was to identify the bioactive compound of Citrus maxima fruit that targets the enzymes responsible for hyperglycaemia. Preliminary in vitro screening of extracts of fruit parts revealed that juicy segments (ethanol, methanol and aqueous) showed the highest inhibition towards the carbohydrate- hydrolysing enzymes. Further, juicy segment extracts were subjected to preparative HPLC for separation and isolation of compounds. After a series of separations, in vitro analysis and characterization, naringin was identified to be the bioactive compound that is responsible for inhibiting carbohydrate-hydrolysing enzyme activities. Further application, such as developing food formulations from C. maxima will benefit diabetic populations.

Keywords


Bioactive Compound, Citrus maxima, Carbohydrate- Hydrolysing Enzymes, Hyperglycaemia.

References





DOI: https://doi.org/10.18520/cs%2Fv114%2Fi10%2F2099-2105