A novel process for obtaining phenylpropanoic acid precursor using Escherichia coli with a constitutive expression system
Phenylpropanoids are widely used in food supplements, pharmaceuticals, and cosmetics with diverse benefits to human health. Trans -cinnamic acid or p -coumaric acid is usually used as the starting precursor to produce phenylpropanoids. Synthetic bioengineering of microbial cell factories offers a su...
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Published in | Food science and biotechnology Vol. 25; no. 3; pp. 795 - 801 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Seoul
The Korean Society of Food Science and Technology
01.06.2016
한국식품과학회 |
Subjects | |
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Abstract | Phenylpropanoids are widely used in food supplements, pharmaceuticals, and cosmetics with diverse benefits to human health.
Trans
-cinnamic acid or
p
-coumaric acid is usually used as the starting precursor to produce phenylpropanoids. Synthetic bioengineering of microbial cell factories offers a sustainable and flexible alternative method for obtaining these compounds. In this study, a constitutive expression system consisting of
Rhodotorula glutinis
phenylalanine/tyrosine ammonia lyase was developed to produce a phenylpropanoic acid precursor in
Escherichia coli
. To improve
trans
-cinnamic acid and
p
-coumaric acid production, BioBrick optimization was investigated, causing a 7.2- and 14.2-fold increase in the yield of these compounds, respectively. The optimum strain was capable of
de novo
producing 78.81 mg/L of
trans
-cinnamic acid and 34.67 mg/L of
p
-coumaric acid in a shake flask culture. The work presented here paves the way for the development of a sustainable and economical process for microbial production of a phenylpropanoic acid precursor. |
---|---|
AbstractList | Phenylpropanoids are widely used in food supplements, pharmaceuticals, and cosmetics with diverse benefits to human health. Trans-cinnamic acid or p-coumaric acid is usually used as the starting precursor to produce phenylpropanoids. Synthetic bioengineering of microbial cell factories offers a sustainable and flexible alternative method for obtaining these compounds. In this study, a constitutive expression system consisting of Rhodotorula glutinis phenylalanine/tyrosine ammonia lyase was developed to produce a phenylpropanoic acid precursor in Escherichia coli. To improve trans-cinnamic acid and p-coumaric acid production, BioBrick optimization was investigated, causing a 7.2- and 14.2-fold increase in the yield of these compounds, respectively. The optimum strain was capable of de novo producing 78.81 mg/L of trans-cinnamic acid and 34.67 mg/L of p-coumaric acid in a shake flask culture. The work presented here paves the way for the development of a sustainable and economical process for microbial production of a phenylpropanoic acid precursor. Phenylpropanoids are widely used in food supplements, pharmaceuticals, and cosmetics with diverse benefits to human health. Trans-cinnamic acid or p-coumaric acid is usually used as the starting precursor to produce phenylpropanoids. Synthetic bioengineering of microbial cell factories offers a sustainable and flexible alternative method for obtaining these compounds. In this study, a constitutive expression system consisting of Rhodotorula glutinis phenylalanine/tyrosine ammonia lyase was developed to produce a phenylpropanoic acid precursor in Escherichia coli. To improve trans-cinnamic acid and p-coumaric acid production, BioBrick optimization was investigated, causing a 7.2- and 14.2-fold increase in the yield of these compounds, respectively. The optimum strain was capable of de novo producing 78.81 mg/L of trans-cinnamic acid and 34.67 mg/L of p-coumaric acid in a shake flask culture. The work presented here paves the way for the development of a sustainable and economical process for microbial production of a phenylpropanoic acid precursor.Phenylpropanoids are widely used in food supplements, pharmaceuticals, and cosmetics with diverse benefits to human health. Trans-cinnamic acid or p-coumaric acid is usually used as the starting precursor to produce phenylpropanoids. Synthetic bioengineering of microbial cell factories offers a sustainable and flexible alternative method for obtaining these compounds. In this study, a constitutive expression system consisting of Rhodotorula glutinis phenylalanine/tyrosine ammonia lyase was developed to produce a phenylpropanoic acid precursor in Escherichia coli. To improve trans-cinnamic acid and p-coumaric acid production, BioBrick optimization was investigated, causing a 7.2- and 14.2-fold increase in the yield of these compounds, respectively. The optimum strain was capable of de novo producing 78.81 mg/L of trans-cinnamic acid and 34.67 mg/L of p-coumaric acid in a shake flask culture. The work presented here paves the way for the development of a sustainable and economical process for microbial production of a phenylpropanoic acid precursor. Phenylpropanoids are widely used in food supplements, pharmaceuticals, and cosmetics with diverse benefits to human health. Trans -cinnamic acid or p -coumaric acid is usually used as the starting precursor to produce phenylpropanoids. Synthetic bioengineering of microbial cell factories offers a sustainable and flexible alternative method for obtaining these compounds. In this study, a constitutive expression system consisting of Rhodotorula glutinis phenylalanine/tyrosine ammonia lyase was developed to produce a phenylpropanoic acid precursor in Escherichia coli . To improve trans -cinnamic acid and p -coumaric acid production, BioBrick optimization was investigated, causing a 7.2- and 14.2-fold increase in the yield of these compounds, respectively. The optimum strain was capable of de novo producing 78.81 mg/L of trans -cinnamic acid and 34.67 mg/L of p -coumaric acid in a shake flask culture. The work presented here paves the way for the development of a sustainable and economical process for microbial production of a phenylpropanoic acid precursor. Phenylpropanoids are widely used in food supplements, pharmaceuticals, and cosmetics with diverse benefits to human health. -cinnamic acid or -coumaric acid is usually used as the starting precursor to produce phenylpropanoids. Synthetic bioengineering of microbial cell factories offers a sustainable and flexible alternative method for obtaining these compounds. In this study, a constitutive expression system consisting of phenylalanine/tyrosine ammonia lyase was developed to produce a phenylpropanoic acid precursor in . To improve -cinnamic acid and -coumaric acid production, BioBrick optimization was investigated, causing a 7.2- and 14.2-fold increase in the yield of these compounds, respectively. The optimum strain was capable of producing 78.81 mg/L of -cinnamic acid and 34.67 mg/L of -coumaric acid in a shake flask culture. The work presented here paves the way for the development of a sustainable and economical process for microbial production of a phenylpropanoic acid precursor. Phenylpropanoids are widely used in food supplements, pharmaceuticals, and cosmetics with diverse benefits to human health. Trans-cinnamic acid or p-coumaric acid is usually used as the starting precursor to produce phenylpropanoids. Synthetic bioengineering of microbial cell factories offers a sustainable and flexible alternative method for obtaining these compounds. In this study, a constitutive expression system consisting of Rhodotorula glutinis phenylalanine/tyrosine ammonia lyase was developed to produce a phenylpropanoic acid precursor in Escherichia coli. To improve transcinnamic acid and p-coumaric acid production, BioBrick optimization was investigated, causing a 7.2- and 14.2-fold increase in the yield of these compounds, respectively. The optimum strain was capable of de novo producing 78.81 mg/L of trans-cinnamic acid and 34.67 mg/L of p-coumaric acid in a shake flask culture. The work presented here paves the way for the development of a sustainable and economical process for microbial production of a phenylpropanoic acid precursor. KCI Citation Count: 2 |
Author | Lin, Junfang Guo, Weixiong Guo, Liqiong Sun, Ping Liang, Jing-long Jiang, Binghua Wan, Hua |
Author_xml | – sequence: 1 givenname: Jing-long surname: Liang fullname: Liang, Jing-long organization: Department of Bioengineering, College of Food Science and Institute of Food Biotechnology, South China Agricultural University, Joint Research & Development Center for Natural Products of Alchemy Biotechnology Co. Ltd. and South China Agricultural University – sequence: 2 givenname: Liqiong surname: Guo fullname: Guo, Liqiong organization: Department of Bioengineering, College of Food Science and Institute of Food Biotechnology, South China Agricultural University, Joint Research & Development Center for Natural Products of Alchemy Biotechnology Co. Ltd. and South China Agricultural University – sequence: 3 givenname: Ping surname: Sun fullname: Sun, Ping organization: Department of Bioengineering, College of Food Science and Institute of Food Biotechnology, South China Agricultural University, Joint Research & Development Center for Natural Products of Alchemy Biotechnology Co. Ltd. and South China Agricultural University – sequence: 4 givenname: Binghua surname: Jiang fullname: Jiang, Binghua organization: Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University – sequence: 5 givenname: Junfang surname: Lin fullname: Lin, Junfang email: linjf@scau.edu.cn organization: Department of Bioengineering, College of Food Science and Institute of Food Biotechnology, South China Agricultural University, Joint Research & Development Center for Natural Products of Alchemy Biotechnology Co. Ltd. and South China Agricultural University – sequence: 6 givenname: Weixiong surname: Guo fullname: Guo, Weixiong organization: Department of Bioengineering, College of Food Science and Institute of Food Biotechnology, South China Agricultural University, Joint Research & Development Center for Natural Products of Alchemy Biotechnology Co. Ltd. and South China Agricultural University – sequence: 7 givenname: Hua surname: Wan fullname: Wan, Hua organization: College of Informatics, South China Agricultural University |
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Cites_doi | 10.2174/187152511796196498 10.1128/AEM.01411-07 10.1016/j.foodchem.2010.05.118 10.1007/s00253-013-5020-9 10.1016/j.procbio.2008.02.001 10.1007/s10295-009-0606-z 10.1126/science.1191652 10.1016/j.jbiotec.2013.07.030 10.1002/bit.24988 10.1128/AEM.02186-10 10.1016/j.ymben.2011.06.005 10.1186/1475-2859-11-153 10.1016/j.foodchem.2010.09.059 10.1016/j.enzmictec.2007.07.025 10.1006/mben.2000.0161 10.1128/AEM.00200-07 10.1073/pnas.1206346109 10.1007/s10529-013-1140-7 10.1016/j.ymben.2005.11.001 10.1128/AEM.02966-14 10.1021/mp7001472 10.1016/j.ymben.2012.11.009 10.1016/j.jbiosc.2014.12.002 10.1016/S0168-9452(01)00490-3 10.1186/1754-1611-2-5 10.1039/c0fo00103a 10.1016/j.foodchem.2011.09.118 10.1128/AEM.00405-15 10.1016/j.copbio.2013.08.009 10.1016/j.ymben.2011.02.002 10.1038/nbt.2355 10.1016/j.jnutbio.2010.07.004 10.1016/j.foodres.2013.01.062 10.1038/nbt.2461 |
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References | Huang, Lin, Yan (CR10) 2013; 110 Vrèek, Bojic, Žuntar, Mendaš, Medic-Šaric (CR7) 2011; 124 Pan, Lai, Ho (CR1) 2010; 1 Limem, Guedonc, Hehn, Bourgaud, Ghedira, Engasser, Ghoul (CR8) 2008; 43 Kim, Kim, Ahn (CR11) 2013; 97 Qi, Haurwitz, Shao, Doudna, Arkin (CR24) 2012; 30 Santos, Xiao, Stephanopoulos (CR27) 2012; 109 Zhou, Du, Chen (CR9) 2014; 25 Kang, Choi, Lee, Hwang, Uhm, Hong (CR33) 2012; 11 Santos, Koffas, Stephanopoulos (CR12) 2011; 13 Wu, Du, Zhou, Chen (CR15) 2013; 16 Jones, Kim, Keasling (CR25) 2000; 2 Duarte-Almeida, Salatino, Genovese, Lajolo (CR6) 2011; 125 Leonard, Yan, Koffas (CR30) 2006; 8 Shetty, Endy, Knight (CR22) 2008; 2 Clere, Faure, Martinez, Andriantsitohaina (CR3) 2011; 9 Leonard, Lim, Saw, Koffas (CR16) 2007; 73 McKenna, Nielsen (CR18) 2011; 13 Bourgaud, Gravot, Milesi, Gontier (CR4) 2001; 161 Awah, Uzoegwu, Ifeonu, Oyugi, Rutherford, Yao, Fehrmann, Fowke, Eze (CR5) 2012; 131 Ajikumar, Xiao, Tyo, Wang, Simeon, Leonard, Mucha, Phon, Pfeifer, Stephanopoulos (CR32) 2010; 330 Jendresen, Stahlhut, Li, Gaspar, Siedler, Forster, Maury, Borodina, Nielsen (CR34) 2015; 81 Leonard, Yan, Fowler, Li, Lim, Lim, Koffas (CR13) 2008; 5 Lim, Fowler, Hueller, Schaffer, Koffas (CR14) 2011; 77 Xue, McCluskey, Cantera, Ben-Bassat, Sariaslani, Huang (CR23) 2007; 42 Van Summeren-Wesenhagen, Marienhagen (CR17) 2015; 81 Gresele, Cerletti, Guglielmini, Pignatelli, Gaetano, Violi (CR2) 2011; 22 Wu, Liu, Fan, Bao, Du, Zhou, Chen (CR20) 2013; 167 Khamduang, Packdibamrung, Chutmanop, Chisti, Srinophakun (CR26) 2009; 36 Zhu, Cui, Fang, Liu, Gao, Zhou (CR29) 2013; 35 Na, Yoo, Chung, Park, Park, Lee (CR21) 2013; 31 Yuan, Cao, Wang, Chen, Li, Ouyang (CR28) 2015; 120 Putignani, Massa, Alisi (CR19) 2013; 54 Leonard, Koffas (CR31) 2007; 73 J Zhou (134_CR9) 2014; 25 L Zhu (134_CR29) 2013; 35 CG Lim (134_CR14) 2011; 77 E Leonard (134_CR30) 2006; 8 E Leonard (134_CR13) 2008; 5 RP Shetty (134_CR22) 2008; 2 JM Duarte-Almeida (134_CR6) 2011; 125 KL Jones (134_CR25) 2000; 2 M Khamduang (134_CR26) 2009; 36 F Bourgaud (134_CR4) 2001; 161 MJ Kim (134_CR11) 2013; 97 L Qi (134_CR24) 2012; 30 R McKenna (134_CR18) 2011; 13 P Yuan (134_CR28) 2015; 120 E Leonard (134_CR31) 2007; 73 Q Huang (134_CR10) 2013; 110 J Wu (134_CR15) 2013; 16 SY Kang (134_CR33) 2012; 11 MH Pan (134_CR1) 2010; 1 P Gresele (134_CR2) 2011; 22 PK Ajikumar (134_CR32) 2010; 330 N Clere (134_CR3) 2011; 9 I Limem (134_CR8) 2008; 43 J Wu (134_CR20) 2013; 167 PV Summeren-Wesenhagen Van (134_CR17) 2015; 81 Z Xue (134_CR23) 2007; 42 IV Vrèek (134_CR7) 2011; 124 L Putignani (134_CR19) 2013; 54 CN Santos (134_CR27) 2012; 109 E Leonard (134_CR16) 2007; 73 D Na (134_CR21) 2013; 31 FM Awah (134_CR5) 2012; 131 CB Jendresen (134_CR34) 2015; 81 CN Santos (134_CR12) 2011; 13 |
References_xml | – volume: 9 start-page: 62 year: 2011 end-page: 77 ident: CR3 article-title: Anticancer properties of flavonoids: Roles in various stages of carcinogenesis publication-title: Cardiovasc. Hematol. Agents Med. Chem. doi: 10.2174/187152511796196498 – volume: 73 start-page: 7246 year: 2007 end-page: 7251 ident: CR31 article-title: Engineering of artificial plant cytochrome P450 enzymes for synthesis of isoflavones by publication-title: Appl. Environ. Microb. doi: 10.1128/AEM.01411-07 – volume: 124 start-page: 354 year: 2011 end-page: 361 ident: CR7 article-title: Phenol content, antioxidant activity and metal composition of Croatian wines deriving from organically and conventionally grown grapes publication-title: Food Chem. doi: 10.1016/j.foodchem.2010.05.118 – volume: 97 start-page: 7195 year: 2013 end-page: 7204 ident: CR11 article-title: Biosynthesis of bioactive O-methylated flavonoids in publication-title: Appl. Microbiol. Biot. doi: 10.1007/s00253-013-5020-9 – volume: 43 start-page: 463 year: 2008 end-page: 479 ident: CR8 article-title: Production of phenylpropanoid compounds by recombinant microorganisms expressing plant-specific biosynthesis genes publication-title: Process Biochem. doi: 10.1016/j.procbio.2008.02.001 – volume: 36 start-page: 1267 year: 2009 end-page: 1274 ident: CR26 article-title: Production of L-phenylalanine from glycerol by a recombinant publication-title: J. Ind. Microbiol. Biotechnol. doi: 10.1007/s10295-009-0606-z – volume: 330 start-page: 70 year: 2010 end-page: 74 ident: CR32 article-title: Isoprenoid pathway optimization for Taxol precursor overproduction in publication-title: Science doi: 10.1126/science.1191652 – volume: 167 start-page: 404 year: 2013 end-page: 411 ident: CR20 article-title: Multivariate modular metabolic engineering of to produce resveratrol from L-tyrosine publication-title: J. Biotechnol. doi: 10.1016/j.jbiotec.2013.07.030 – volume: 110 start-page: 3188 year: 2013 end-page: 3196 ident: CR10 article-title: Caffeic acid production enhancement by engineering a phenylalanine over-producing strain publication-title: Biotechnol. Bioeng. doi: 10.1002/bit.24988 – volume: 77 start-page: 3451 year: 2011 end-page: 3460 ident: CR14 article-title: High-yield resveratrol production in engineered publication-title: Appl. Environ. Microb. doi: 10.1128/AEM.02186-10 – volume: 13 start-page: 544 year: 2011 end-page: 554 ident: CR18 article-title: Styrene biosynthesis from glucose by engineered publication-title: Metab. Eng. doi: 10.1016/j.ymben.2011.06.005 – volume: 11 start-page: 153 year: 2012 ident: CR33 article-title: Artificial biosynthesis of phenylpropanoic acids in a tyrosine overproducing strain publication-title: Microb. Cell Fact. doi: 10.1186/1475-2859-11-153 – volume: 125 start-page: 660 year: 2011 end-page: 664 ident: CR6 article-title: Phenolic composition and antioxidant activity of culms and sugarcane (Saccharum officinarum L.) products publication-title: Food Chem. doi: 10.1016/j.foodchem.2010.09.059 – volume: 42 start-page: 58 year: 2007 end-page: 64 ident: CR23 article-title: Improved production of p-hydroxycinnamic acid from tyrosine using a novel thermostable phenylalanine/tyrosine ammonia lyase enzyme publication-title: Enzyme. Microb. Tech. doi: 10.1016/j.enzmictec.2007.07.025 – volume: 2 start-page: 328 year: 2000 end-page: 338 ident: CR25 article-title: Low-copy plasmids can perform as well as or better than high-copy plasmids for metabolic engineering of bacteria publication-title: Metab. Eng. doi: 10.1006/mben.2000.0161 – volume: 73 start-page: 3877 year: 2007 end-page: 3886 ident: CR16 article-title: Engineering central metabolic pathways for high-level flavonoid production in publication-title: Appl. Environ. Microb. doi: 10.1128/AEM.00200-07 – volume: 109 start-page: 13538 year: 2012 end-page: 13543 ident: CR27 article-title: Rational, combinatorial, and genomic approaches for engineering L-tyrosine production in publication-title: P. Natl. Acad. Sci. USA doi: 10.1073/pnas.1206346109 – volume: 35 start-page: 751 year: 2013 end-page: 756 ident: CR29 article-title: Cloning, expression and characterization of phenylalanine ammonia-lyase from Rhodotorula glutinis publication-title: Biotechnol. Lett. doi: 10.1007/s10529-013-1140-7 – volume: 8 start-page: 172 year: 2006 end-page: 181 ident: CR30 article-title: Functional expression of a P450 flavonoid hydroxylase for the biosynthesis of plant-specific hydroxylated flavonols in publication-title: Metab. Eng. doi: 10.1016/j.ymben.2005.11.001 – volume: 81 start-page: 840 year: 2015 end-page: 849 ident: CR17 article-title: Metabolic engineering of for the synthesis of the plant polyphenol pinosylvin publication-title: Appl. Environ. Microb. doi: 10.1128/AEM.02966-14 – volume: 5 start-page: 257 year: 2008 end-page: 265 ident: CR13 article-title: Strain improvement of recombinant for efficient production of plant flavonoids publication-title: Mol. Pharm. doi: 10.1021/mp7001472 – volume: 16 start-page: 48 year: 2013 end-page: 55 ident: CR15 article-title: Metabolic engineering of for (2S)-pinocembrin production from glucose by a modular metabolic strategy publication-title: Metab. Eng. doi: 10.1016/j.ymben.2012.11.009 – volume: 120 start-page: 36 year: 2015 end-page: 40 ident: CR28 article-title: Enhancement of Lphenylalanine production by engineered using phased exponential L-tyrosine feeding combined with nitrogen source optimization publication-title: J. Biosci. Bioeng. doi: 10.1016/j.jbiosc.2014.12.002 – volume: 161 start-page: 839 year: 2001 end-page: 851 ident: CR4 article-title: Production of plant secondary metabolites: A historical perspective publication-title: Plant Sci. doi: 10.1016/S0168-9452(01)00490-3 – volume: 2 start-page: 5 year: 2008 ident: CR22 article-title: Engineering BioBrick vectors from BioBrick parts publication-title: J. Biol. Eng. doi: 10.1186/1754-1611-2-5 – volume: 1 start-page: 15 year: 2010 end-page: 31 ident: CR1 article-title: Anti-inflammatory activity of natural dietary flavonoids publication-title: Food Funct. doi: 10.1039/c0fo00103a – volume: 131 start-page: 1279 year: 2012 end-page: 1286 ident: CR5 article-title: Free radical scavenging activity, phenolic contents and cytotoxicity of selected Nigerian medicinal plants publication-title: Food Chem. doi: 10.1016/j.foodchem.2011.09.118 – volume: 81 start-page: 4458 year: 2015 end-page: 4476 ident: CR34 article-title: Highly active and specific tyrosine ammonia-lyases from diverse origins enable enhanced production of aromatic compounds in bacteria and publication-title: Appl. Environ. Microb. doi: 10.1128/AEM.00405-15 – volume: 25 start-page: 17 year: 2014 end-page: 23 ident: CR9 article-title: Novel fermentation processes for manufacturing plant natural products publication-title: Curr. Opin. Biotech. doi: 10.1016/j.copbio.2013.08.009 – volume: 13 start-page: 392 year: 2011 end-page: 400 ident: CR12 article-title: Optimization of a heterologous pathway for the production of flavonoids from glucose publication-title: Metab. Eng. doi: 10.1016/j.ymben.2011.02.002 – volume: 30 start-page: 1002 year: 2012 end-page: 1006 ident: CR24 article-title: RNA processing enables predictable programming of gene expression publication-title: Nat. Biotechnol. doi: 10.1038/nbt.2355 – volume: 22 start-page: 201 year: 2011 end-page: 211 ident: CR2 article-title: Effects of resveratrol and other wine polyphenols on vascular function: An update publication-title: J. Nutr. Biochem. doi: 10.1016/j.jnutbio.2010.07.004 – volume: 54 start-page: 1084 year: 2013 end-page: 1095 ident: CR19 article-title: Engineered as new source of flavonoids and terpenoids publication-title: Food Res. Int. doi: 10.1016/j.foodres.2013.01.062 – volume: 31 start-page: 170 year: 2013 end-page: 174 ident: CR21 article-title: Metabolic engineering of using synthetic small regulatory RNAs publication-title: Nat. Biotechnol. doi: 10.1038/nbt.2461 – volume: 110 start-page: 3188 year: 2013 ident: 134_CR10 publication-title: Biotechnol. Bioeng. doi: 10.1002/bit.24988 – volume: 125 start-page: 660 year: 2011 ident: 134_CR6 publication-title: Food Chem. doi: 10.1016/j.foodchem.2010.09.059 – volume: 13 start-page: 544 year: 2011 ident: 134_CR18 publication-title: Metab. Eng. doi: 10.1016/j.ymben.2011.06.005 – volume: 97 start-page: 7195 year: 2013 ident: 134_CR11 publication-title: Appl. Microbiol. Biot. doi: 10.1007/s00253-013-5020-9 – volume: 9 start-page: 62 year: 2011 ident: 134_CR3 publication-title: Cardiovasc. Hematol. Agents Med. Chem. doi: 10.2174/187152511796196498 – volume: 124 start-page: 354 year: 2011 ident: 134_CR7 publication-title: Food Chem. doi: 10.1016/j.foodchem.2010.05.118 – volume: 73 start-page: 3877 year: 2007 ident: 134_CR16 publication-title: Appl. Environ. Microb. doi: 10.1128/AEM.00200-07 – volume: 8 start-page: 172 year: 2006 ident: 134_CR30 publication-title: Metab. Eng. doi: 10.1016/j.ymben.2005.11.001 – volume: 109 start-page: 13538 year: 2012 ident: 134_CR27 publication-title: P. Natl. Acad. Sci. USA doi: 10.1073/pnas.1206346109 – volume: 13 start-page: 392 year: 2011 ident: 134_CR12 publication-title: Metab. Eng. doi: 10.1016/j.ymben.2011.02.002 – volume: 11 start-page: 153 year: 2012 ident: 134_CR33 publication-title: Microb. Cell Fact. doi: 10.1186/1475-2859-11-153 – volume: 167 start-page: 404 year: 2013 ident: 134_CR20 publication-title: J. Biotechnol. doi: 10.1016/j.jbiotec.2013.07.030 – volume: 42 start-page: 58 year: 2007 ident: 134_CR23 publication-title: Enzyme. Microb. Tech. doi: 10.1016/j.enzmictec.2007.07.025 – volume: 16 start-page: 48 year: 2013 ident: 134_CR15 publication-title: Metab. Eng. doi: 10.1016/j.ymben.2012.11.009 – volume: 25 start-page: 17 year: 2014 ident: 134_CR9 publication-title: Curr. Opin. Biotech. doi: 10.1016/j.copbio.2013.08.009 – volume: 120 start-page: 36 year: 2015 ident: 134_CR28 publication-title: J. Biosci. Bioeng. doi: 10.1016/j.jbiosc.2014.12.002 – volume: 1 start-page: 15 year: 2010 ident: 134_CR1 publication-title: Food Funct. doi: 10.1039/c0fo00103a – volume: 73 start-page: 7246 year: 2007 ident: 134_CR31 publication-title: Appl. Environ. Microb. doi: 10.1128/AEM.01411-07 – volume: 161 start-page: 839 year: 2001 ident: 134_CR4 publication-title: Plant Sci. doi: 10.1016/S0168-9452(01)00490-3 – volume: 77 start-page: 3451 year: 2011 ident: 134_CR14 publication-title: Appl. Environ. Microb. doi: 10.1128/AEM.02186-10 – volume: 2 start-page: 5 year: 2008 ident: 134_CR22 publication-title: J. Biol. Eng. doi: 10.1186/1754-1611-2-5 – volume: 54 start-page: 1084 year: 2013 ident: 134_CR19 publication-title: Food Res. Int. doi: 10.1016/j.foodres.2013.01.062 – volume: 2 start-page: 328 year: 2000 ident: 134_CR25 publication-title: Metab. Eng. doi: 10.1006/mben.2000.0161 – volume: 5 start-page: 257 year: 2008 ident: 134_CR13 publication-title: Mol. Pharm. doi: 10.1021/mp7001472 – volume: 31 start-page: 170 year: 2013 ident: 134_CR21 publication-title: Nat. Biotechnol. doi: 10.1038/nbt.2461 – volume: 81 start-page: 840 year: 2015 ident: 134_CR17 publication-title: Appl. Environ. Microb. doi: 10.1128/AEM.02966-14 – volume: 30 start-page: 1002 year: 2012 ident: 134_CR24 publication-title: Nat. Biotechnol. doi: 10.1038/nbt.2355 – volume: 131 start-page: 1279 year: 2012 ident: 134_CR5 publication-title: Food Chem. doi: 10.1016/j.foodchem.2011.09.118 – volume: 36 start-page: 1267 year: 2009 ident: 134_CR26 publication-title: J. Ind. Microbiol. Biotechnol. doi: 10.1007/s10295-009-0606-z – volume: 35 start-page: 751 year: 2013 ident: 134_CR29 publication-title: Biotechnol. Lett. doi: 10.1007/s10529-013-1140-7 – volume: 330 start-page: 70 year: 2010 ident: 134_CR32 publication-title: Science doi: 10.1126/science.1191652 – volume: 43 start-page: 463 year: 2008 ident: 134_CR8 publication-title: Process Biochem. doi: 10.1016/j.procbio.2008.02.001 – volume: 81 start-page: 4458 year: 2015 ident: 134_CR34 publication-title: Appl. Environ. Microb. doi: 10.1128/AEM.00405-15 – volume: 22 start-page: 201 year: 2011 ident: 134_CR2 publication-title: J. Nutr. Biochem. doi: 10.1016/j.jnutbio.2010.07.004 |
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Snippet | Phenylpropanoids are widely used in food supplements, pharmaceuticals, and cosmetics with diverse benefits to human health.
Trans
-cinnamic acid or
p
-coumaric... Phenylpropanoids are widely used in food supplements, pharmaceuticals, and cosmetics with diverse benefits to human health. -cinnamic acid or -coumaric acid is... Phenylpropanoids are widely used in food supplements, pharmaceuticals, and cosmetics with diverse benefits to human health. Trans-cinnamic acid or p-coumaric... |
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SubjectTerms | ammonia bioengineering Chemistry Chemistry and Materials Science cosmetics culture flasks dietary supplements drugs Escherichia coli Food Science gene expression human health Nutrition p-coumaric acid phenylalanine phenylpropanoids Rhodotorula glutinis tyrosine 식품과학 |
Title | A novel process for obtaining phenylpropanoic acid precursor using Escherichia coli with a constitutive expression system |
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