Multicellular living organisms and unmodified parts thereof and – Plant – seedling – plant seed – or plant part – per se – Higher plant – seedling – plant seed – or plant part
Reexamination Certificate
2000-09-22
2004-01-06
McElwain, Elizabeth F. (Department: 1638)
Multicellular living organisms and unmodified parts thereof and
Plant, seedling, plant seed, or plant part, per se
Higher plant, seedling, plant seed, or plant part
C800S281000, C435S419000, C435S468000, C435S471000, C435S252300, C536S023200, C536S023600
Reexamination Certificate
active
06673988
ABSTRACT:
FIELD OF THE INVENTION
This invention is in the field of plant molecular biology. More specifically, this invention pertains to nucleic acid fragments encoding lipases in plants and seeds.
BACKGROUND OF THE INVENTION
True lipases act at an oil-water interface; they constitute a ubiquitous group of enzymes catalyzing a wide variety of reactions, many with industrial potential. Lipases have been grouped into families according to their amino acid sequence, enzymatic specificity, and differential expression. A family of lipolytic enzymes with members in
Arabidopsis thaliana
, rice and corn has been described (Brick et al. (1995)
FEBS Lett.
377:475-480).
It is possible to change the structure of fats and oils by manipulating the lipase specificity ending with products containing the desired fatty acid at a specific position on the glycerol backbone. Lipases play important roles in pathogen defense and in activating membrane formation.
The lipase sequences presented herein also contain similarities to the alfalfa early nodule-specific gene ENOD8, which is activated soon after rhizobium infection. Corn and rice EST sequences having similarities to lipases that are found in the NCBI database having General Identifier Nos. 569288, 570021, 702247, 3763803, 3763804, 3768136, 4715132, 4716417, 4827484, 5455457, 5455577, 5455582, and 5455586.
Identification of cDNAs encoding lipases in crops will allow their manipulation, and thus, the creation of plants with oils of different fatty acid composition.
SUMMARY OF THE INVENTION
The present invention concerns an isolated polynucleotide comprising a nucleotide sequence selected from the group consisting of: (a) a first nucleotide sequence encoding a polypeptide of at least 157 amino acids having at least 80% identity based on the Clustal method of alignment when compared to a polypeptide selected from the group consisting of SEQ ID NOs:2, 4, 6, and 8, or (b) a second nucleotide sequence comprising the complement of the first nucleotide sequence.
In a second embodiment, it is preferred that the isolated polynucleotide of the claimed invention comprises a first nucleotide sequence which comprises a nucleic acid sequence selected from the group consisting of SEQ ID NOs:1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, and 37 that codes for the polypeptide selected from the group consisting of SEQ ID NOs:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40.
In a third embodiment, this invention concerns an isolated polynucleotide comprising a nucleotide sequence of at least one of 60 (preferably at least one of 40, most preferably at least one of 30) contiguous nucleotides derived from a nucleotide sequence selected from the group consisting of SEQ ID NOs:1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, and 37 and the complement of such nucleotide sequences.
In a fourth embodiment, this invention relates to a chimeric gene comprising an isolated polynucleotide of the present invention operably linked to at least one suitable regulatory sequence.
In a fifth embodiment, the present invention concerns an isolated host cell comprising a chimeric gene of the present invention or an isolated polynucleotide of the present invention. The host cell may be eukaryotic, such as a yeast or a plant cell, or prokaryotic, such as a bacterial cell. The present invention also relates to a virus, preferably a baculovirus, comprising an isolated polynucleotide of the present invention or a chimeric gene of the present invention.
In a sixth embodiment, the invention also relates to a process for producing an isolated host cell comprising a chimeric gene of the present invention or an isolated polynucleotide of the present invention, the process comprising either transforming or transfecting an isolated compatible host cell with a chimeric gene or isolated polynucleotide of the present invention.
In a seventh embodiment, the invention concerns a lipase polypeptide of at least 157 amino acids comprising at least 80% identity based on the Clustal method of alignment compared to a polypeptide selected from the group consisting of SEQ ID NOs:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40.
In an eighth embodiment, the invention relates to a method of selecting an isolated polynucleotide that affects the level of expression of a lipase polypeptide or enzyme activity in a host cell, preferably a plant cell, the method comprising the steps of: (a) constructing an isolated polynucleotide of the present invention or an isolated chimeric gene of the present invention; (b) introducing the isolated polynucleotide or the isolated chimeric gene into a host cell; (c) measuring the level of the lipase polypeptide or enzyme activity in the host cell containing the isolated polynucleotide; and (d) comparing the level of the lipase polypeptide or enzyme activity in the host cell containing the isolated polynucleotide with the level of the lipase polypeptide or enzyme activity in the host cell that does not contain the isolated polynucleotide.
In a ninth embodiment, the invention concerns a method of obtaining a nucleic acid fragment encoding a substantial portion of a lipase polypeptide, preferably a plant lipase polypeptide, comprising the steps of: synthesizing an oligonucleotide primer comprising a nucleotide sequence of at least one of 60 (preferably at least one of 40, most preferably at east one of 30) contiguous nucleotides derived from a nucleotide sequence selected from the group consisting of SEQ ID NOs:1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, and 37, and the complement of such nucleotide sequences; and amplifying a nucleic acid fragment (preferably a cDNA inserted in a cloning vector) using the oligonucleotide primer. The amplified nucleic acid fragment preferably will encode a substantial portion of a lipase amino acid sequence.
In a tenth embodiment, this invention relates to a method of obtaining a nucleic acid fragment encoding all or a substantial portion of the amino acid sequence encoding a lipase polypeptide comprising the steps of: probing a cDNA or genomic library with an isolated polynucleotide of the present invention; identifying a DNA clone that hybridizes with an isolated polynucleotide of the present invention; isolating the identified DNA clone; and sequencing the cDNA or genomic fragment that comprises the isolated DNA clone.
In an eleventh embodiment, this invention concerns a composition, such as a hybridization mixture, comprising an isolated polynucleotide of the present invention.
In a twelfth embodiment, this invention concerns a method for positive selection of a transformed cell comprising: (a) transforming a host cell with the chimeric gene of the present invention or an expression cassette of the present invention; and (b) growing the transformed host cell, preferably a plant cell, such as a monocot or a dicot, under conditions which allow expression of the lipase polynucleotide in an amount sufficient to complement a null mutant to provide a positive selection means.
In a thirteenth embodiment, this invention relates to a method of altering the level of expression of a lipase in a host cell comprising: (a) transforming a host cell with a chimeric gene of the present invention; and (b) growing the transformed host cell under conditions that are suitable for expression of the chimeric gene wherein expression of the chimeric gene results in production of altered levels of the lipase in the transformed host cell.
REFERENCES:
Chris Upton et al, TIBS20—May 1995, pp. 178-179 “A New Family of Lipolytic Enzymes?”.
Bork et al, Trends in Genetics, vol. 12, No. 10: 425-427, Oct. 1996.*
Brenner, S.E., Trends in Genetics, Vol 15, No. 4: 132-133, Apr. 1999.*
Smith et al, Nature Biotechnology, vol. 15: 1222-1223, Nov. 1997.*
Doerks et al, Trends in Genetics, vol. 14, No. 6: 248-250, Jun. 1998.*
Van de Loo et al, Proc. Natl, Acad. Sci, USA, vol. 92: 6743-6747, Jul. 1995.*
Broun et al, Science, vol. 282: 131-133, Nov. 13, 1998.*
DeLuca, V., AgBio
E. I. du Pont de Nemours and Company
McElwain Elizabeth F.
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