Processing biomass
US-2015353974-A1 · Dec 10, 2015 · US
US2016115507A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016115507-A1 |
| Application number | US-201414890423-A |
| Country | US |
| Kind code | A1 |
| Filing date | May 9, 2014 |
| Priority date | May 10, 2013 |
| Publication date | Apr 28, 2016 |
| Grant date | — |
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The present invention relates to a novel isolated polypeptide having the ability to export O-phosphoserine (OPS) that is a precursor of L-cysteine, a vector comprising the polynucleotide, an OPS-producing microorganism having enhanced activity of the polypeptide, a method of producing OPS using the microorganism, and a method for preparing cysteine or its derivatives, which comprises reacting OPS, produced by the above method, with a sulfide in the presence of O-phosphoserine sulfhydrylase (OPSS) or a microorganism that expresses OPSS.
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1 . A method for producing O-phosphoserine (OPS), comprising culturing an O-phosphoserine-producing microorganism having enhanced activity of a polypeptide that has an amino acid sequence of SEQ ID NO: 1 or 2 and has O-phosphoserine exporting activity. 2 . The method according to claim 1 , wherein the O-phosphoserine-producing microorganism further has reduced activity of endogenous phosphoserine phosphatase. 3 . The method according to claim 1 , wherein the O-phosphoserine-producing microorganism further has enhanced activity of phosphoglycerate dehydrogenase or phosphoserine aminotransferase. 4 . An isolated polypeptide having an amino acid sequence of SEQ ID NO: 1 or 2 and having O-phosphoserine (OPS) exporting activity. 5 . A polynucleotide encoding the polypeptide of claim 4 . 6 . A vector comprising the polynucleotide of claim 5 . 7 . An O-phosphoserine-producing microorganism having enhanced activity of a polypeptide that has an amino acid sequence of SEQ ID NO: 1 or 2 and has O-phosphoserine exporting activity. 8 . The microorganism of claim 7 , wherein the microorganism further has reduced activity of endogenous phosphoserine phosphatase. 9 . The microorganism according to claim 7 , wherein the microorganism further has enhanced activity of phosphoglycerate dehydrogenase or phosphoserine aminotransferase. 10 . A method for producing cysteine or its derivatives, comprising the steps of: a) culturing the microorganism of claim 7 to produce O-phosphoserine (OPS); and b) reacting the O-phosphoserine, produced in step a), with a sulfide in the presence of O-phosphoserine sulfhydrylase (OPSS) or a microorganism that expresses OPSS. 11 . The method according to claim 10 , wherein the sulfide is one or more selected from the group consisting of Na 2 S, NaSH, (NH 4 ) 2 S, H 2 S and Na 2 S 2 O 3 . 12 . A method for producing cysteine or its derivatives, comprising the steps of: a) culturing the microorganism of claim 8 to produce O-phosphoserine (OPS); and b) reacting the O-phosphoserine, produced in step a), with a sulfide in the presence of O-phosphoserine sulfhydrylase (OPSS) or a microorganism that expresses OPSS. 13 . The method according to claim 12 , wherein the sulfide is one or more selected from the group consisting of Na 2 S, NaSH, (NH 4 ) 2 S, H 2 S and Na 2 S 2 O 3 . 14 . A method for producing cysteine or its derivatives, comprising the steps of: a) culturing the microorganism of claim 9 to produce O-phosphoserine (OPS); and b) reacting the O-phosphoserine, produced in step a), with a sulfide in the presence of O-phosphoserine sulfhydrylase (OPSS) or a microorganism that expresses OPSS. 15 . The method according to claim 14 , wherein the sulfide is one or more selected from the group consisting of Na 2 S, NaSH, (NH 4 ) 2 S, H 2 S and Na 2 S 2 O 3 .
Methionine; Cysteine; Cystine · CPC title
Alanine; Leucine; Isoleucine; Serine; Homoserine · CPC title
Escherichia (G) · CPC title
DNA or RNA fragments; Modified forms thereof (DNA or RNA not used in recombinant technology, C07H21/00); {Non-coding nucleic acids having a biological activity} · CPC title
from bacteria · CPC title
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