PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2009 | 31 | 1 |

Tytuł artykułu

Partial purification and characterization of pectinmethylesterase from ripening guava (Psidium guajava L.) fruits

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Employing the techniques of (NH₄)₂SO₄ fractionation, ion exchange chromatography on DEAE cellulose and gel filtration through Sephadex G-100, pectinmethylesterase (EC 3.1.1.11) was purified from guava (Psidium guajava L.) fruits var. Hisar Safeda harvested at turning stage of maturity to 129-fold with 28% recovery. Molecular weight as determined by gel filtration was found to be 51 kDa and the enzyme preparation exhibited the same molecular weight under native (Native-PAGE) and denaturating conditions (SDS-PAGE) indicating that the enzyme was a monomer. With pectin as the substrate, it exhibited the Michaelis Menten kinetics with Km value of 3.1 g l⁻¹. The enzyme was found to be stimulated by Ca⁺⁺ and Na⁺ and inhibited competitively by Dgalacturonic acid with Ki value of 1.97 mM. The enzyme was completely inactivated by iodine while with diethyl pyrocarbonate and N-acetylimidazole, the enzyme was inhibited up to the extent of 56 and 45%, respectively. However, DTNB had no inhibitory effect whatsoever precluding the participation of any –SH group in the active centre. It is tentatively proposed that the enzyme has tyrosine and histidine residues at its active centre.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

31

Numer

1

Opis fizyczny

p.81-87,fig.,ref.

Twórcy

autor
  • Plant Biochemistry and Molecular Biology Laboratory, Department of Biochemistry, CCS Haryana Agricultural University, Hisar 125 004, Haryana, India
  • Plant Biochemistry and Molecular Biology Laboratory, Department of Biochemistry, CCS Haryana Agricultural University, Hisar 125 004, Haryana, India
autor
  • Plant Biochemistry and Molecular Biology Laboratory, Department of Biochemistry, CCS Haryana Agricultural University, Hisar 125 004, Haryana, India
autor
  • Plant Biochemistry and Molecular Biology Laboratory, Department of Biochemistry, CCS Haryana Agricultural University, Hisar 125 004, Haryana, India

Bibliografia

  • Alonso J, Rodriguez MT, Canet W (1995) Effect of calcium pretreatments in the texture of frozen cherries. Role of pectinesterase in the changes in the pectic materials. J Agric Food Chem 43:1011–1016. doi:10.1021/jf00052a031
  • Alonso J, Rodriguez MT, Canet W (1996) Purification and characterization of four pectinesterases from sweet cherry (Prunus avium L.). J Agric Food Chem 44:3416–3422. doi:10.1021/jf960204s
  • Alonso J, Howell N, Canet W (1997) Purification and characterization of two pectinmethylesterase from persimmon (Diospyros kaki). J Sci Food Agric 75:352–358. doi:10.1002/(SICI)1097-0010 (199711)75:3<352::AID-JSFA885>3.0.CO;2-G
  • Amaral SHD, Assis SADE, Oliveira OMMDEF (2005) partial purification and characterization of pectin methylesterase from orange (Citrus sinensis). J Food Biochem 29:367–380. doi: 10.1111/j.1745-4514.2005.00036.x
  • Awad M (1985) Persimmon pectinmethylesterase: extraction and variation during ripening. J Food Sci 56:743–746
  • Bordenave M, Goldberg R (1993) Purification and characterization of pectin methylesterases from mung bean hypocotyl cell walls. Phytochemical 33:999–1003. doi:10.1016/0031-9422(93)85011-F
  • Brady CJ (1976) The pectinesterase of the pulp of the banana fruit. Aust J Plant Physiol 3:163–172
  • Buescher RW, Furmanski RJ (1978) Role of pectinesterase and polygalacturonase in the formation of woolliness in peaches. J Food Sci 43:264–266. doi:10.1111/j.1365-2621.1978.tb09788.x
  • Chang LWS, Morita LL, Yamamoto HY (1965) Papaya pectinesterase inhibition by sucrose. J Food Sci 30:218–222. doi: 10.1111/j.1365-2621.1965.tb00292.x
  • Davis BJ (1964) Disc electrophoresis II. Method and application to human serum proteins. Ann N Y Acad Sci 121:404–427. doi: 10.1111/j.1749-6632.1964.tb14213.x
  • El-Zoghbi M (1994) Biochemical changes in some tropical fruits during ripening. Food Chem 49:33–37. doi:10.1016/0308-8146(94)90229-1
  • Gafe J, Morvan C, Jauneau A, Demarty M (1992) Partial purification of flax cell wall pectin methylesterase. Phytochemical 31:761–765
  • Giovane A, Quagliuolo L, Castaldo D, Servillo L, Balestrieri C (1990) Pectin methyl esterase from Actinidia chinensis fruit. Phytochemical 29:2821–2823. doi:10.1016/0031-9422(90)87083-7
  • Hagerman AE, Austin PJ (1986) Continuous spectrophotometric assay for plant pectin methyl esterase. J Agric Food Chem 34:440–444. doi:10.1021/jf00069a015
  • Jain N, Dhawan K, Malhotra S, Singh R (2001) Compositional and enzymatic changes in guava (Psidium guajava L.) fruits during ripening. Acta Physiol Plant 23:357–362. doi:10.1007/s11738-001-0044-7
  • Jain N, Dhawan K, Malhotra S, Singh R (2003) Biochemistry of fruit ripening of guava (Psidium guajava L.): compositional and enzymatic changes. Plant Foods Hum Nutr 58:309–315. doi: 10.1023/B:QUAL.0000040285.50062.4b
  • Jansen EF, MacDonnell RL (1945) Influence of methoxyl content of pectic substances on the action of polygalacturonase. Arch Biochem 8:97–112
  • Jansen EF, Jang R, Bonner J (1960) Orange pectinesterase binding and activity. Food Res 25:64
  • Javeri H, Wicker L (1991) Partial puyrification and characterization of peach pectinesterase. J Food Biochem 15:241–252. doi: 10.1111/j.1745-4514.1991.tb00159.x
  • Koch JL, Nevins DJ (1989) Tomato fruit cell wall. I. Use of purified tomato polygalacturonase and pectin methyl esterase to identify developmental changes in pectins. Plant Physiol 91:816–822
  • Komae K, Sone Y, Kakuta M, Misaki A (1990) Purification and characterization of pectinesterase from Ficus awkeotsang. Agric Biol Chem 54:1469–1476
  • Laemmili UK (1970) Cleavage of structural proteins during the assembly of head bacteriophage T4. Nature 277:680–685. doi: 10.1038/227680a0
  • Laratta B, De Masi L, Minasi P, Giovane A (2008) Pectin methylesterase in Citrus bergamia R.: purification, biochemical characterisation and sequence of the exon related to the enzyme active site. Food Chem 110:829–837. doi:10.1016/j.foodchem. 2008.02.065
  • Lin TP, Liu C-C, Chen SW, Wang WY (1991) Purification and characterization of pectinmethylesterase from Ficus awkeotsang makino achenes. Plant Physiol 91:1445–1453
  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with folin phenol reagent. J Biol Chem 193:265–275
  • MacDonald HM, Evans R, Spencer WJ (1993) Purification and properties of the major pectinesterases in lemon fruits (Citrus limon). J Sci Food Agric 62:163–168. doi:10.1002/jsfa. 2740620209
  • Marcus L, Schejter A (1983) Single step chromatographia purification and characterization of the endopolygalacturonases and pectinesterases of the fungus, Botrytis cinerea pers. Physiol Plant Pathol 22:1–13
  • Markovic O, Jornvall H (1986) Pectinesterase. The primary structure of the tomato enzyme. Eur J Biochem 158:455–462. doi: 10.1111/j.1432-1033.1986.tb09775.x
  • Markovic O, Patoka J (1977) Experientia (Basel) 33:711–712. (c.f. Markovic and Jornvall 1986)
  • Missang CE, Baron A, Renard CMGC (2004) Cell wall degrading enzymes and changes in cell wall polysaccharides during ripening and storage of bush butter (Dacryodes edulis (G. Don) H.J. Lam) fruit. J Hort Sci Biotech 79(5):797–805
  • Moustacas A, Nari J, Borel M, Noat G, Ricard J (1991) Pectin methylesterase, metal ions in plant cell wall extension. Biochem J 279:351–354
  • Nari J, Noat G, Ricard J (1991) Pectin methylesterase, metal ions and plant cell wall extension. Biochem J 279:343–350
  • Nighojkar A, Srivastava S, Kumar A (1994) Pectin methyl esterase from germinating Vigna sinensis seeds. Plant Sci 103:115–120
  • Nunes CS, Castro SM, Jorge A, Manuel A, Coimbra ME, Hendrickx AM, Van L (2006) Thermal and high-pressure stability of purified pectin methylesterase from plums (Prunus domestica). J Food Biochem 30:138–154
  • Rexova-Benkova L, Markovic O (1976) Pectic enzymes. Adv Cabohydr Chem Biochem 33:323–385
  • Rouse AH, Atkins CD, Moore EL (1960) Effect of pectinesterase on the stability of frozen concentrated orange juice. Proc Fla State Hort Soc 73: 271 (c.f. Chang et al. 1965)

Uwagi

Rekord w opracowaniu

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-3235cc32-ce9f-46ae-b1a3-77f43c9150f9
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.