Literature DB >> 17002458

Mode of de-esterification of alkaline and acidic pectin methyl esterases at different pH conditions.

Thomas Duvetter1, Ilse Fraeye, Daniel N Sila, Isabel Verlent, Chantal Smout, Marc Hendrickx, Ann Van Loey.   

Abstract

Highly esterified citrus pectin was de-esterified at pH 4.5 and 8.0 by a fungal pectin methyl esterase (PME) that was shown to have an acidic isoelectric pH (pI) and an acidic pH optimum and by a plant PME that was characterized by an alkaline pI and an alkaline pH optimum. Interchain and intrachain de-esterification patterns were studied by digestion of the pectin products with endo-polygalacturonase and subsequent analysis using size exclusion and anion-exchange chromatography. No effect of pH was observed on the de-esterification mode of either of the two enzymes. Acidic, fungal PME converted pectin according to a multiple-chain mechanism, with a limited degree of multiple attack at the intrachain level, both at pH 4.5 and at pH 8.0. A multiple-attack mechanism, with a high degree of multiple attack, was more appropriate to describe the action mode of alkaline, plant PME, both at pH 4.5 and at pH 8.0.

Mesh:

Substances:

Year:  2006        PMID: 17002458     DOI: 10.1021/jf060013h

Source DB:  PubMed          Journal:  J Agric Food Chem        ISSN: 0021-8561            Impact factor:   5.279


  7 in total

1.  Structure and functional features of olive pollen pectin methylesterase using homology modeling and molecular docking methods.

Authors:  Jose C Jimenez-Lopez; Simeon O Kotchoni; María I Rodríguez-García; Juan D Alché
Journal:  J Mol Model       Date:  2012-06-22       Impact factor: 1.810

2.  Molecular Cloning, Expression and Characterization of Pectin Methylesterase (CtPME) from Clostridium thermocellum.

Authors:  Vikky Rajulapati; Arun Goyal
Journal:  Mol Biotechnol       Date:  2017-05       Impact factor: 2.695

3.  Tuning of Pectin Methylesterification: PECTIN METHYLESTERASE INHIBITOR 7 MODULATES THE PROCESSIVE ACTIVITY OF CO-EXPRESSED PECTIN METHYLESTERASE 3 IN A pH-DEPENDENT MANNER.

Authors:  Fabien Sénéchal; Mélanie L'Enfant; Jean-Marc Domon; Emeline Rosiau; Marie-Jeanne Crépeau; Ogier Surcouf; Juan Esquivel-Rodriguez; Paulo Marcelo; Alain Mareck; François Guérineau; Hyung-Rae Kim; Jozef Mravec; Estelle Bonnin; Elisabeth Jamet; Daisuke Kihara; Patrice Lerouge; Marie-Christine Ralet; Jérôme Pelloux; Catherine Rayon
Journal:  J Biol Chem       Date:  2015-07-16       Impact factor: 5.157

4.  Structure and Properties of a Non-processive, Salt-requiring, and Acidophilic Pectin Methylesterase from Aspergillus niger Provide Insights into the Key Determinants of Processivity Control.

Authors:  Lisa M Kent; Trevor S Loo; Laurence D Melton; Davide Mercadante; Martin A K Williams; Geoffrey B Jameson
Journal:  J Biol Chem       Date:  2015-11-14       Impact factor: 5.157

5.  Molecular basis of the activity of the phytopathogen pectin methylesterase.

Authors:  Markus Fries; Jessica Ihrig; Keith Brocklehurst; Vladimir E Shevchik; Richard W Pickersgill
Journal:  EMBO J       Date:  2007-08-23       Impact factor: 11.598

6.  Reassessment of chitosanase substrate specificities and classification.

Authors:  Tobias Weikert; Anna Niehues; Stefan Cord-Landwehr; Margareta J Hellmann; Bruno M Moerschbacher
Journal:  Nat Commun       Date:  2017-11-22       Impact factor: 14.919

Review 7.  Pectin Methylesterases: Cell Wall Remodeling Proteins Are Required for Plant Response to Heat Stress.

Authors:  Hui-Chen Wu; Victor P Bulgakov; Tsung-Luo Jinn
Journal:  Front Plant Sci       Date:  2018-11-06       Impact factor: 5.753

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.