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human fp gene sequence  (GenScript corporation)

 
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    GenScript corporation human fp gene sequence
    Human Fp Gene Sequence, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fp+genes/human+mut+gene/pmc12273924-31-0-15
    Average 90 stars, based on 1 article reviews
    human fp gene sequence - by Bioz Stars, 2026-09
    90/100 stars

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    Synthesized:

    Article Title: Stabilization of Near-Infrared Fluorescent Proteins by Packaging in Virus-like Particles.
    Article Snippet: Near-IR fluorescent Qβ virus-like particles (VLPs) were produced in a high yield by packaging highly red-shifted monomeric and dimeric versions of biliverdin-dependent fluorescent proteins within the capsid shell.. The simple addition of biliverdin hydrochloride to the medium during or after Escherichia coli protein expression was enough to produce fully matured encapsidated fluorophores.. The packaged near-IR proteins exhibited identical photochemical properties to their nonencapsidated analogues but were far more stable toward heat, chaotropeinduced denaturation, and proteolysis.

    Expressing:

    Article Title: Stabilization of Near-Infrared Fluorescent Proteins by Packaging in Virus-like Particles.
    Article Snippet: Near-IR fluorescent Qβ virus-like particles (VLPs) were produced in a high yield by packaging highly red-shifted monomeric and dimeric versions of biliverdin-dependent fluorescent proteins within the capsid shell.. The simple addition of biliverdin hydrochloride to the medium during or after Escherichia coli protein expression was enough to produce fully matured encapsidated fluorophores.. The packaged near-IR proteins exhibited identical photochemical properties to their nonencapsidated analogues but were far more stable toward heat, chaotropeinduced denaturation, and proteolysis.



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    a Illustration of the modularized platform for producing and exporting rubusoside. Module A (terpene synthesis module) incorporates modifications designed to divert carbon flux to diterpene metabolic and brought ent-kaurene biosynthesis. Engineering yeast into the efficient platform to produce rubusoside by introducing Module B (P450s module) and Module C (rubusoside synthesis module). Module D (UDP-glucose synthesis module) provides glycoside ligands for producing rubusoside. Module E (rubusoside exporter module) is a possible exportation system of rubusoside. ERG10 acetyl-CoA C-acetyltransferase, ERG13 hydroxymethylglutaryl-CoA synthase, HMG1 hydroxymethylglutaryl-CoA reductase, tHMG1 truncated hydroxymethylglutaryl-CoA reductase, ERG12 mevalonate kinase, ERG8 phosphomevalonate kinase, IDI1 isopentenyl diphosphate delta-isomerase, ERG20 bifunctional (2E,6E)-farnesyl diphosphate, BST1 farnesyltranstransferase, KS kaurene synthase, KO ent-kaurene oxidase, KAH kaurenoic acid 13α-hydroxylase, UGT74G1 UDP-glycosyltransferase 74G1, UGT85C2 UDP-glycosyltransferase 85C2. FPS <t>F112A</t> mutant farnesyl pyrophosphate synthase. Glc-6-P glucose-6-phosphate, Acetyl-CoA acetyl coenzyme A, IPP isopentenyl diphosphate, GPP Geranyl diphosphate, FPP farnesyl diphosphate, GGPP geranylgeranyl pyrophosphate, DMAPP dimethylallyl diphosphate, EKA ent-kaurenoic acid, 13-SMG (5ξ,8α,9ξ,10α,13α)-13-(β-D-Glucopyranosyloxy) kaur-16-en-18-säure, 19-SMG 1-O-[(5ξ,8α,9ξ,10α,13α)-13-Hydroxy-18-oxokaur-16-én-18-yl]-β-D-glucopyranose. All the heterologous genes were controlled by GAL promoters. b Increased ent-kaurene biosynthesis by eliminating the rate-limiting steps in MVA pathway (overexpressed tHMG1 and IDI1 , SGN02) and avoiding competition for FPP with the monoterpene synthesis pathway (introduced FPS F112A , SGN03). All the heterologous genes were controlled by GAL promoters. c HPLC spectra of ent-kaurenoic acid (EKA), steviol, rubusoside, and their standards. RT retention time. d LC-MS analysis results of EKA, steviol, and rubusoside in negative ion mode. Source data are provided as a Source Data file. e The rubusoside titer difference in the intracellular and extracellular of the SGN06 strain. b , e Data are presented as mean values ± SD from three independent biological replicates ( n = 3), the circles represent individual data points. Significance ( p -value) was evaluated by two-sided t -test.
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    a Illustration of the modularized platform for producing and exporting rubusoside. Module A (terpene synthesis module) incorporates modifications designed to divert carbon flux to diterpene metabolic and brought ent-kaurene biosynthesis. Engineering yeast into the efficient platform to produce rubusoside by introducing Module B (P450s module) and Module C (rubusoside synthesis module). Module D (UDP-glucose synthesis module) provides glycoside ligands for producing rubusoside. Module E (rubusoside exporter module) is a possible exportation system of rubusoside. ERG10 acetyl-CoA C-acetyltransferase, ERG13 hydroxymethylglutaryl-CoA synthase, HMG1 hydroxymethylglutaryl-CoA reductase, tHMG1 truncated hydroxymethylglutaryl-CoA reductase, ERG12 mevalonate kinase, ERG8 phosphomevalonate kinase, IDI1 isopentenyl diphosphate delta-isomerase, ERG20 bifunctional (2E,6E)-farnesyl diphosphate, BST1 farnesyltranstransferase, KS kaurene synthase, KO ent-kaurene oxidase, KAH kaurenoic acid 13α-hydroxylase, UGT74G1 UDP-glycosyltransferase 74G1, UGT85C2 UDP-glycosyltransferase 85C2. FPS <t>F112A</t> mutant farnesyl pyrophosphate synthase. Glc-6-P glucose-6-phosphate, Acetyl-CoA acetyl coenzyme A, IPP isopentenyl diphosphate, GPP Geranyl diphosphate, FPP farnesyl diphosphate, GGPP geranylgeranyl pyrophosphate, DMAPP dimethylallyl diphosphate, EKA ent-kaurenoic acid, 13-SMG (5ξ,8α,9ξ,10α,13α)-13-(β-D-Glucopyranosyloxy) kaur-16-en-18-säure, 19-SMG 1-O-[(5ξ,8α,9ξ,10α,13α)-13-Hydroxy-18-oxokaur-16-én-18-yl]-β-D-glucopyranose. All the heterologous genes were controlled by GAL promoters. b Increased ent-kaurene biosynthesis by eliminating the rate-limiting steps in MVA pathway (overexpressed tHMG1 and IDI1 , SGN02) and avoiding competition for FPP with the monoterpene synthesis pathway (introduced FPS F112A , SGN03). All the heterologous genes were controlled by GAL promoters. c HPLC spectra of ent-kaurenoic acid (EKA), steviol, rubusoside, and their standards. RT retention time. d LC-MS analysis results of EKA, steviol, and rubusoside in negative ion mode. Source data are provided as a Source Data file. e The rubusoside titer difference in the intracellular and extracellular of the SGN06 strain. b , e Data are presented as mean values ± SD from three independent biological replicates ( n = 3), the circles represent individual data points. Significance ( p -value) was evaluated by two-sided t -test.
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    a Illustration of the modularized platform for producing and exporting rubusoside. Module A (terpene synthesis module) incorporates modifications designed to divert carbon flux to diterpene metabolic and brought ent-kaurene biosynthesis. Engineering yeast into the efficient platform to produce rubusoside by introducing Module B (P450s module) and Module C (rubusoside synthesis module). Module D (UDP-glucose synthesis module) provides glycoside ligands for producing rubusoside. Module E (rubusoside exporter module) is a possible exportation system of rubusoside. ERG10 acetyl-CoA C-acetyltransferase, ERG13 hydroxymethylglutaryl-CoA synthase, HMG1 hydroxymethylglutaryl-CoA reductase, tHMG1 truncated hydroxymethylglutaryl-CoA reductase, ERG12 mevalonate kinase, ERG8 phosphomevalonate kinase, IDI1 isopentenyl diphosphate delta-isomerase, ERG20 bifunctional (2E,6E)-farnesyl diphosphate, BST1 farnesyltranstransferase, KS kaurene synthase, KO ent-kaurene oxidase, KAH kaurenoic acid 13α-hydroxylase, UGT74G1 UDP-glycosyltransferase 74G1, UGT85C2 UDP-glycosyltransferase 85C2. FPS <t>F112A</t> mutant farnesyl pyrophosphate synthase. Glc-6-P glucose-6-phosphate, Acetyl-CoA acetyl coenzyme A, IPP isopentenyl diphosphate, GPP Geranyl diphosphate, FPP farnesyl diphosphate, GGPP geranylgeranyl pyrophosphate, DMAPP dimethylallyl diphosphate, EKA ent-kaurenoic acid, 13-SMG (5ξ,8α,9ξ,10α,13α)-13-(β-D-Glucopyranosyloxy) kaur-16-en-18-säure, 19-SMG 1-O-[(5ξ,8α,9ξ,10α,13α)-13-Hydroxy-18-oxokaur-16-én-18-yl]-β-D-glucopyranose. All the heterologous genes were controlled by GAL promoters. b Increased ent-kaurene biosynthesis by eliminating the rate-limiting steps in MVA pathway (overexpressed tHMG1 and IDI1 , SGN02) and avoiding competition for FPP with the monoterpene synthesis pathway (introduced FPS F112A , SGN03). All the heterologous genes were controlled by GAL promoters. c HPLC spectra of ent-kaurenoic acid (EKA), steviol, rubusoside, and their standards. RT retention time. d LC-MS analysis results of EKA, steviol, and rubusoside in negative ion mode. Source data are provided as a Source Data file. e The rubusoside titer difference in the intracellular and extracellular of the SGN06 strain. b , e Data are presented as mean values ± SD from three independent biological replicates ( n = 3), the circles represent individual data points. Significance ( p -value) was evaluated by two-sided t -test.
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    a Illustration of the modularized platform for producing and exporting rubusoside. Module A (terpene synthesis module) incorporates modifications designed to divert carbon flux to diterpene metabolic and brought ent-kaurene biosynthesis. Engineering yeast into the efficient platform to produce rubusoside by introducing Module B (P450s module) and Module C (rubusoside synthesis module). Module D (UDP-glucose synthesis module) provides glycoside ligands for producing rubusoside. Module E (rubusoside exporter module) is a possible exportation system of rubusoside. ERG10 acetyl-CoA C-acetyltransferase, ERG13 hydroxymethylglutaryl-CoA synthase, HMG1 hydroxymethylglutaryl-CoA reductase, tHMG1 truncated hydroxymethylglutaryl-CoA reductase, ERG12 mevalonate kinase, ERG8 phosphomevalonate kinase, IDI1 isopentenyl diphosphate delta-isomerase, ERG20 bifunctional (2E,6E)-farnesyl diphosphate, BST1 farnesyltranstransferase, KS kaurene synthase, KO ent-kaurene oxidase, KAH kaurenoic acid 13α-hydroxylase, UGT74G1 UDP-glycosyltransferase 74G1, UGT85C2 UDP-glycosyltransferase 85C2. FPS F112A mutant farnesyl pyrophosphate synthase. Glc-6-P glucose-6-phosphate, Acetyl-CoA acetyl coenzyme A, IPP isopentenyl diphosphate, GPP Geranyl diphosphate, FPP farnesyl diphosphate, GGPP geranylgeranyl pyrophosphate, DMAPP dimethylallyl diphosphate, EKA ent-kaurenoic acid, 13-SMG (5ξ,8α,9ξ,10α,13α)-13-(β-D-Glucopyranosyloxy) kaur-16-en-18-säure, 19-SMG 1-O-[(5ξ,8α,9ξ,10α,13α)-13-Hydroxy-18-oxokaur-16-én-18-yl]-β-D-glucopyranose. All the heterologous genes were controlled by GAL promoters. b Increased ent-kaurene biosynthesis by eliminating the rate-limiting steps in MVA pathway (overexpressed tHMG1 and IDI1 , SGN02) and avoiding competition for FPP with the monoterpene synthesis pathway (introduced FPS F112A , SGN03). All the heterologous genes were controlled by GAL promoters. c HPLC spectra of ent-kaurenoic acid (EKA), steviol, rubusoside, and their standards. RT retention time. d LC-MS analysis results of EKA, steviol, and rubusoside in negative ion mode. Source data are provided as a Source Data file. e The rubusoside titer difference in the intracellular and extracellular of the SGN06 strain. b , e Data are presented as mean values ± SD from three independent biological replicates ( n = 3), the circles represent individual data points. Significance ( p -value) was evaluated by two-sided t -test.

    Journal: Nature Communications

    Article Title: De novo biosynthesis of rubusoside and rebaudiosides in engineered yeasts

    doi: 10.1038/s41467-022-30826-2

    Figure Lengend Snippet: a Illustration of the modularized platform for producing and exporting rubusoside. Module A (terpene synthesis module) incorporates modifications designed to divert carbon flux to diterpene metabolic and brought ent-kaurene biosynthesis. Engineering yeast into the efficient platform to produce rubusoside by introducing Module B (P450s module) and Module C (rubusoside synthesis module). Module D (UDP-glucose synthesis module) provides glycoside ligands for producing rubusoside. Module E (rubusoside exporter module) is a possible exportation system of rubusoside. ERG10 acetyl-CoA C-acetyltransferase, ERG13 hydroxymethylglutaryl-CoA synthase, HMG1 hydroxymethylglutaryl-CoA reductase, tHMG1 truncated hydroxymethylglutaryl-CoA reductase, ERG12 mevalonate kinase, ERG8 phosphomevalonate kinase, IDI1 isopentenyl diphosphate delta-isomerase, ERG20 bifunctional (2E,6E)-farnesyl diphosphate, BST1 farnesyltranstransferase, KS kaurene synthase, KO ent-kaurene oxidase, KAH kaurenoic acid 13α-hydroxylase, UGT74G1 UDP-glycosyltransferase 74G1, UGT85C2 UDP-glycosyltransferase 85C2. FPS F112A mutant farnesyl pyrophosphate synthase. Glc-6-P glucose-6-phosphate, Acetyl-CoA acetyl coenzyme A, IPP isopentenyl diphosphate, GPP Geranyl diphosphate, FPP farnesyl diphosphate, GGPP geranylgeranyl pyrophosphate, DMAPP dimethylallyl diphosphate, EKA ent-kaurenoic acid, 13-SMG (5ξ,8α,9ξ,10α,13α)-13-(β-D-Glucopyranosyloxy) kaur-16-en-18-säure, 19-SMG 1-O-[(5ξ,8α,9ξ,10α,13α)-13-Hydroxy-18-oxokaur-16-én-18-yl]-β-D-glucopyranose. All the heterologous genes were controlled by GAL promoters. b Increased ent-kaurene biosynthesis by eliminating the rate-limiting steps in MVA pathway (overexpressed tHMG1 and IDI1 , SGN02) and avoiding competition for FPP with the monoterpene synthesis pathway (introduced FPS F112A , SGN03). All the heterologous genes were controlled by GAL promoters. c HPLC spectra of ent-kaurenoic acid (EKA), steviol, rubusoside, and their standards. RT retention time. d LC-MS analysis results of EKA, steviol, and rubusoside in negative ion mode. Source data are provided as a Source Data file. e The rubusoside titer difference in the intracellular and extracellular of the SGN06 strain. b , e Data are presented as mean values ± SD from three independent biological replicates ( n = 3), the circles represent individual data points. Significance ( p -value) was evaluated by two-sided t -test.

    Article Snippet: The codon-optimized genes KS (NCBI Accession Number: Q9UVY5 ), FPS F112A (NCBI Accession Number: P08836.2 ), KO (NCBI Accession Number: AAQ63464.1 ), KAH (NCBI Accession Number: NP_197872.1 ) , CPR1 (NCBI Accession Number: ABB88839.2 ), UGT74G1 (NCBI Accession Number: Q6VAA6.1 ), UGT85C2 (NCBI Accession Number: Q6VAB0.1 ), UGT91D2 (NCBI Accession Number: B3VI56.1 ), UGT76G1 (NCBI Accession Number: AGL95113.1 ), and EUGT11 (NCBI Accession Number: XP_015629141.1 ) were synthesized by GenScript.

    Techniques: Mutagenesis, Liquid Chromatography with Mass Spectroscopy