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The invention represents the disclosure of a novel insect intestinal mucin comprising two nearly identical isoforms, IIM14 and IIM22 respectively. These isoforms of the IIM protein have been identified and cloned using T. ni larva. The cDNA and amino acid sequences have been determined and are disclosed. Both IIM isoforms have an approximate molecular mass of 400 kDa. These sequences once disclosed are useful for the production of transgenic or recombinant vectors including viral, microorganism cell, plant, or animals, wherein the virus, microorganism, cell, plant, or animal is the product of an insertion of a gene expression vector including a DNA that encodes an IIM protein sequence. Thereafter the engineered host of the IIM DNA sequence is capable of expressing said IIM protein in a functional form. Also useful is a purified and isolated recombinant DNA sequence comprising a DNA sequence that codes for an IIM protein. The recombinant DNA sequence used can be a cDNA sequence for...

InventorsRobert R. Granados, Ping Wang
Original AssigneeBoyce Thompson Institute for Plant Research, Inc.
Primary Examiner: Richard Schnizer
Current U.S. Classification435/69.1; 435/252.3; 435/320.1; 435/325; 536/23.5
International Classification: C12P 2106; C12N 120; C12N 1500; C12N 500; C07H 2104

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Referenced by

Citing PatentFiling dateIssue dateOriginal AssigneeTitle
US6833350Jan 30, 2001Dec 21, 2004Nestec S.A.Method for maintaining or improving the synthesis of mucins

Claims

1. An isolated polynucleotide encoding an invertebrate intestinal mucin comprising an amino acid sequence selected from the group consisting of:

a) SEQ ID No. 3; and
b) SEQ ID No. 4.

2. An isolated polynucleotide encoding an invertebrate intestinal mucin, said polynucleotide comprising a nucleotide sequence selected from the group consisting of:

a) SEQ ID No. 1; and
b) SEQ ID No. 2.

3. An expression vector comprising an expression control sequence operatively linked to the polynucleotide of claim 1 or claim 2.

4. An isolated host cell comprising the expression vector of claim 3.

5. The expression vector of claim 3, wherein the expression vector is a bacterial expression vector.

6. The expression vector of claim 3, wherein the expression vector is a plant expression vector.

7. A method of producing an invertebrate intestinal mucin protein or peptide comprising:

a) transforming a host cell with an expression vector comprising a promoter operatively linked to a nucleotide sequence, wherein the nucleotide sequence encodes an amino acid sequence selected from the group consisting of:
i) SEQ ID No. 3; and
ii) SEQ ID No. 4;

or wherein the nucleotide sequence encodes a peptide comprised by a sequence selected from the group consisting of:
iii) SEQ ID No. 3; and
iv) SEQ ID No. 4;
b) culturing said host cell under conditions that allow expression of said invertebrate intestinal mucin protein or peptide in recoverable quantity;
c) lysing said host cell; and
d) recovering said invertebrate intestinal mucin protein or peptide.

8. The method of claim 7 wherein said expression vector encodes a fusion protein comprising the invertebrate intestinal mucin protein or peptide and glutathione-S-transferase.