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Tove M.I.E. Christensen

Researcher at Danisco

Publications -  19
Citations -  1641

Tove M.I.E. Christensen is an academic researcher from Danisco. The author has contributed to research in topics: Pectin & Esterase. The author has an hindex of 13, co-authored 19 publications receiving 1553 citations. Previous affiliations of Tove M.I.E. Christensen include Nielsen Holdings N.V. & University of Leeds.

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Journal ArticleDOI

Modulation of the Degree and Pattern of Methyl-esterification of Pectic Homogalacturonan in Plant Cell Walls IMPLICATIONS FOR PECTIN METHYL ESTERASE ACTION, MATRIX PROPERTIES, AND CELL ADHESION

TL;DR: It is demonstrated that, in addition to blockwise de-esterification, HG with a non-blockwise distribution of methyl esters is also an abundant feature of HG in primary plant cell walls, implications for understanding of both the action of pectin methyl esterases on matrix properties and mechanisms of intercellular adhesion and its loss in plants.
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Analysis of pectic epitopes recognised by hybridoma and phage display monoclonal antibodies using defined oligosaccharides, polysaccharides, and enzymatic degradation

TL;DR: Investigation of the structure of epitopes recognised by anti-pectin monoclonal antibodies found that optimal JIM5 and JIM7 binding occurs where specific but undefined methyl-esterification patterns are present on HG domains, although fully de-esterified HG samples contain sub-optimal J IM5 epitopes.
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Analysis of different de-esterification mechanisms for pectin by enzymatic fingerprinting using endopectin lyase and endopolygalacturonase II from A. niger.

TL;DR: Introduction of a certain pattern of methyl ester distribution caused by selective removal of certain methyl Ester groups by f-PME is the most reasonable explanation for the detected differences.
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Chemically methylated and reduced pectins: preparation, characterisation by 1H NMR spectroscopy, enzymatic degradation, and gelling properties.

TL;DR: New modified pectin have been prepared by treatment of pectins having different DM with NaBH(4) to reduce selectively the methyl esters to primary alcohols in the presence of free acids and exhibit high gelling properties.
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Quantification of the amount of galacturonic acid residues in blocksequences in pectin homogalacturonan by enzymatic fingerprinting with exo- and endo-polygalacturonase II from Aspergillus niger.

TL;DR: Differences between the amounts of galacturonic acid located in exo- and endo-BS, provided evidence for the need of a certain start side or blocklength for p-PME to de-esterify blockwise.