The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Sep. 28, 2010

Filed:

Nov. 20, 2007
Applicants:

Brett J. Savary, Jonesboro, AR (US);

Randall G. Cameron, Thonotosassa, FL (US);

Gary A. Luzio, Winter Haven, FL (US);

Thomas G. Mccollum, Vero Beach, FL (US);

Prasanna Vasu, Jonesboro, AR (US);

Alberto Nunez, Dresher, PA (US);

Inventors:

Brett J. Savary, Jonesboro, AR (US);

Randall G. Cameron, Thonotosassa, FL (US);

Gary A. Luzio, Winter Haven, FL (US);

Thomas G. McCollum, Vero Beach, FL (US);

Prasanna Vasu, Jonesboro, AR (US);

Alberto Nunez, Dresher, PA (US);

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
C12N 9/00 (2006.01); C12N 9/16 (2006.01); C12N 9/18 (2006.01); C12N 1/20 (2006.01); C12N 15/00 (2006.01); C07H 21/04 (2006.01);
U.S. Cl.
CPC ...
Abstract

Enzymes accumulated in plant cell walls serve diverse physiological functions including metabolism, polysaccharide structure modification, and molecular communication in interactions with other organisms. Pectin methylesterases are economically important enzymes for their impact on quality and processing properties of fruit and vegetable food products. We have now purified TT-PME to homogeneity from sweet orange finisher pulp and determined the complete corresponding nucleic acid sequence. Purified TT-PME was observed by SDS-PAGE as two doublet bands with molecular masses of approximately 46,000 Da and 56,000 Da. Direct Edman sequencing from these proteins showed a common N-terminal peptide. De novo sequencing of eight TT-PME tryptic peptides determined by MALDI-TOF/TOF mass spectrometry provided additional internal sequences. TT-PME did not correspond to any previously reportedspp. PME sequence. Our results showTT-PME is a distinctive new isoform with phylogenetic relationship closer to PME isoforms in other species rather than to previously describedPME genes.


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