IP Library Granted Patent US 10,364,421
Granted Patent B2
US 10,364,421 · App. 15/548,812 · Granted Jul 30, 2019

Modified glucoamylase enzymes and yeast strains having enhanced bioproduct production

Inventors: Christopher K. Miller (Andover, MN); Ana Negrete-Raymond (Chanhassen, MN); Jon Veldhouse (Plymouth, MN); Amit Vas (Minneapolis, MN)
Assignee: CARGILL, INCORPORATED
C12N9/2428C07K14/395C12N9/16C12P19/14C12Y301/03002C07K2319/02Y02E50/17
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Quick Facts
Patent No.
US 10,364,421
App. No.
15/548,812
Granted
Jul 30, 2019
Kind
B2
Abstract

The invention is directed to non-natural yeast able to secrete significant amounts of glucoamylase into a fermentation media. The glucoamylase can promote degradation of starch material generating glucose for fermentation to a desired bioproduct, such as ethanol. The glucoamylase can be provided in the form of a glucoamylase fusion protein having a S. cerevisiae mating factor alpha 2 (Sc MFα2) or repressible acid phosphatase (Sc PHO5) secretion signal.

Claims (14)

1. A polypeptide comprising (a) a secretion signal amino acid sequence having 90% or greater identity to SEQ ID NO:10 or SEQ ID NO:11 and (b) a glucoamylase amino acid sequence from a yeast, fungal, or bacterial glucoamylase polypeptide, wherein the polypeptide has glucoamylase activity, and

wherein the polypeptide comprises SEQ ID NO: 13.

2. A polypeptide comprising:

(a) a secretion signal amino acid sequence comprising SEQ ID NO:10 or SEQ ID NO:11 and

(b) a glucoamylase amino acid sequence from a yeast, fungal, or bacterial glucoamylase polypeptide, wherein the polypeptide has glucoamylase activity, and wherein the glucoamylase amino acid sequence in (b) comprises amino acids 19-515 of SEQ ID NO:12.

3. A polypeptide comprising (a) a secretion signal amino acid sequence having 90% or greater identity to SEQ ID NO:10 or SEQ ID NO:11 and (b) a glucoamylase amino acid sequence from a yeast, fungal, or bacterial glucoamylase polypeptide, wherein the polypeptide has glucoamylase activity, and

wherein the polypeptide comprises SEQ ID NO:14.

4. The polypeptide of claim 1 further comprising a third sequence that is different than SEQ ID NO:10, amino acids 1-18 of SEQ ID NO: 12, or the glucoamylase amino acid sequence, wherein the third sequence is positioned between SEQ ID NO:10 and the glucoamylase amino acid sequence.

5. A host cell that expresses the polypeptide of claim 1 .

6. The host cell of claim 5 wherein the host cell is a strain of Saccharomyces cerevisiae.

7. The host cell of claim 6 which is (a) tolerant to growth in fermentation medium having a concentration of ethanol of greater than 90 g/L, (b) tolerant to growth in at temperatures of greater than 33° C., such as in the range of 34° C.-40° C., or both (a) and (b).

8. The polypeptide of claim 4 , wherein the third sequence is a linker sequence that prevents interactions between the secretion signal amino acid sequence and the glucoamylase amino acid sequence.

9. The polypeptide of claim 3 further comprising a third sequence that is different than SEQ ID NO:11, amino acids 1-18 of SEQ ID NO: 12, or the glucoamylase amino acid sequence, wherein the third sequence is positioned between SEQ ID NO:11 and the glucoamylase amino acid sequence.

10. The polypeptide of claim 9 , wherein the third sequence is a linker sequence that prevents interactions between the secretion signal amino acid sequence and the glucoamylase amino acid sequence.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 2, 2017
From: MILLER, CHRISTOPHER KENNETH; NEGRETE-RAYMOND, ANA; VELDHOUSE, JONATHAN DWIGHT; VAS, AMIT
To: CARGILL, INCORPORATED
Reel/Frame 043753/0193 →
Continuity (2)
Provisional Application 62112807 · Feb 6, 2015
Related Publication 20180080014A1 · Mar 22, 2018
Cited By (1)
US 12,529,079