Generated by SRI International Pathway Tools Version 25.0 on Sat Jun 12, 2021

Total Page:16

File Type:pdf, Size:1020Kb

Generated by SRI International Pathway Tools Version 25.0 on Sat Jun 12, 2021 Authors: Pallavi Subhraveti Ron Caspi Peter Midford Peter D Karp An online version of this diagram is available at BioCyc.org. Biosynthetic pathways are positioned in the left of the cytoplasm, degradative pathways on the right, and reactions not assigned to any pathway are in the far right of the cytoplasm. Transporters and membrane proteins are shown on the membrane. Ingrid Keseler Periplasmic (where appropriate) and extracellular reactions and proteins may also be shown. Pathways are colored according to their cellular function. Gcf_001746795Cyc: Piscirickettsia salmonis AY3800B Cellular Overview Connections between pathways are omitted for legibility. Anamika Kothari lipid II (meso diaminopimelate 2+ phosphate Mg containing) Co 2+ RS00065 RS15145 RS08855 RS08330 RS08105 RS07905 RS07160 RS06550 RS14225 RS05365 RS05005 FliQ RS13580 RS04095 RS03695 RS03315 RS03070 RS12345 TypA RS12050 RS01480 RS11100 RS11015 RS01215 RS10860 RS10620 RS08655 MurJ RS10415 RS10330 RS00450 RS10075 IcmP RS09985 RS09920 ApaG RS09870 RS00235 RS10015 RS10055 RS10080 RS10195 RS10405 RS10445 RS10515 RS10565 RS01040 RS01160 RS10950 FtsW RS01465 RS01705 RS02185 TolR RS02840 RS03190 RS03595 RS03945 RS04280 RS04650 RS13705 RS05285 RS05680 RS06165 RS06945 RS07480 RS10305 RS08640 MlaE RS09600 lipid II (meso Mg 2+ diaminopimelate phosphate Co 2+ containing) RS01875 RS09935 Macromolecule Modification glutaminyl-tRNA gln Aminoacyl-tRNA Charging 6 α L-alanyl-γ-D- tRNA-uridine 2-thiolation ATP biosynthesis Carbohydrate Degradation N -(3-methylbut- a nascent peptidoglycan UDP-N-acetyl- -D- a nascent UDP-N-acetyl- phosphoenol a nucleoside an L-cysteinyl- biosynthesis via transamidation a sulfurated γ a lipid II H O γ 2-en-1-yl)- with (L-alanyl- -D-glutamyl- muramoyl-L-alanyl- peptidoglycan glutamyl-meso- UDP-N-acetyl- α-D-muramoyl- 2 RNA -L-glutamyl- gly Cys and selenation (bacteria) [sulfur carrier] GTP dGDP pyruvate triphosphate ATP roseoflavin [tRNA ] RS02295 RS09970 Secondary Metabolite Biosynthesis adenosine 37 meso-2,6-diaminopimeloyl-D- γ-D-glutamyl-meso- (meso-DAP diaminopimelate α-D-muramate L-alanyl-γ-D- D-alanine ADP D-galactose degradation I (Leloir pathway) D-alanyl-D-alanine 5'-phosphate glu N-acetylneuraminate and in tRNA alanyl-D-alanine) pentapeptide 2,6-diaminopimelate containing) glutamyl-meso-2,6- cys F0F1 ATP synthase: penicillin- preQ biosynthesis N-acetylmannosamine UDP-N- diaminopimeloyl- DNA- glutathione aminoacyl- 0 AVM72_RS13010 atpB β-D-galactopyranose binding ribosome myo-inositol degradation I tRNA (N6-isopentenyl D-alanyl-D-alanine directed RNA bifunctional tRNA IscS subfamily atpE AVM72_RS13025 penicillin-binding UDP-N- endolytic acetylmuramate:L- protein biogenesis pyruvate synthase: biosynthesis N-acetylneuraminate adenosine(37)-C2)- polymerase riboflavin hydrolase: TolB RS10020 cysteine AVM72_RS13030 protein 2: mrdA acetylmuramoyl- transglycosylase alanyl-gamma-D- 2: mrdA GTPase kinase: pyk gshB GTP D-glucopyranose N-acetylneuraminate methylthiotransferase subunit kinase/FAD pth gln an L-glutamyl- desulfurase: AVM72_RS13035 atpG D-alanyl-D-alanine tripeptide--D-alanyl- MltG: mltG glutamyl- meso- penicillin- D-alanyl-D-alanine Der: der glutathione 6-phosphate lyase: MiaB: miaB omega: rpoZ synthetase: [tRNA Gln ] AVM72_RS02310 carboxypeptidase/ D- alanine ligase: lytic murein diaminopimelate binding [+ 3 isozymes] synthase: GTP cyclohydrolase I atpD AVM72_RS13050 α carboxypeptidase/ + + -D-galactopyranose AVM72_RS14570 succinate AVM72_RS12905 ligase: mpl [+ 3 isozymes] ribF H RS04195 H Asp-tRNA(Asn) FolE2: AVM72_RS07325 cysteine N-acetyl-D- D-alanyl-D-alanine- transglycosylase protein D-alanyl-D-alanine- pyruvate gshB Asp-tRNA(Asn) dehydrogenase, Cys /Glu-tRNA(Gln) 7,8-dihydroneopterin 3'-triphosphate ATP mannosamine endopeptidase: dacB B: mltB 2: mrdA dGTP cys a tRNA RS04215 RS10085 /Glu-tRNA(Gln) desulfurase: galactokinase: endopeptidase: dacB H + amidotransferase: Ins(3)P hydrophobic α phosphate roseoflavin N-acetylmannosamine UDP-N-acetyl- -D- UDP-N-acetyl- GDP + + amidotransferase: AVM72_RS04815 AVM72_RS01485 membrane anchor D-alanyl-D-alanine RNA adenine H RS05225 H gatB gatA gatC 6-carboxytetrahydropterin an [L-cysteine kinase: muramoyl-L-alanyl- α-D-muramoyl- norophthalmate gatB gatA gatC inositol protein: sdhD a nascent peptidoglycan a mature a nascent carboxypeptidase/ a N- dinucleotide [+ 5 isozymes] synthase: AVM72_RS00325 desulfurase]-S- AVM72_RS14560 γ γ-D-glutamyl-meso- L-alanyl-γ-D- a 5-phosphooxy- monophosphatase: α-D-galactose 1-phosphate UDP-α-D-glucose with (L-alanyl- -D-glutamyl- D-ala peptidoglycan peptidoglycan D-alanyl-D-alanine- D-ala acetylglucosamine- 6-carboxytetrahydropterin sulfanyl-L-cysteine N-acetyl-D- 6 2,6-diaminopimeloyl- glutamyl-meso-2,6- RS13570 RS10100 L-glutamyl- AVM72_RS02300 N -(3-methylbut- meso-2,6-diaminopimeloyl- with (L-alanyl- (meso-DAP endopeptidase: dacB -N-acetylmuramyl- + F0F1 ATP + ammonium an unsulfurated H H [tRNA Gln ] synthase: AVM72_RS11575 mannosamine 5'-deoxyadenosine 2-en-1-yl)-2- met D-alanine) tetrapeptide D-alanyl-D-alanine γ-D-glutamyl- containing) with diaminopimelate (tetrapeptide) synthase myo-inositol 6-phosphate [sulfur carrier] GlcNAc terminus 6-carboxy-5,6,7,8-tetrahydropterin (methylsulfanyl) meso-2,6- UDP-N- pyrophosphoryl- putative N- 37 Asp-tRNA(Asn) a [TusA sulfur- adenosine diaminopimeloyl- D-ala acetylmuramoyl- undecaprenol acetylmannosamine- /Glu-tRNA(Gln) carrier protein]-S- in tRNA D-alanine) L-alanyl-γ-D- RS00095 RS04955 RS00660 7-carboxy-7-deazaguanine 6-phosphate amidotransferase: sulfanyl-L-cysteine tetrapeptide glutamyl-meso-2,6- synthase QueE: queE 2-epimerase: gatB gatA gatC sulfurtransferase diaminopimeloyl- RS09795 AVM72_RS14555 7-carboxy-7-deazaguanine complex: tusD D-alanine tusC TusB N-acetyl-D- an L-glutaminyl- tRNA charging glucosamine RS05750 RS10465 Gln 7-cyano-7-deazaguanine a [TusD sulfur- RS09620 [tRNA ] γ α synthase: AVM72_RS02645 carrier protein]-S- 6-phosphate a nascent peptidoglycan a peptidoglycan a peptidoglycan dimer (meso N-acetyl-muramoyl-(L- L-alanyl- -D- a [bis(guanylyl UDP-N-acetyl- phosphoenol an [apo BCAA N-acetyl- - menadione NADH H + a [glutamine- RS09660 sulfanyl-L-cysteine α with (L-alanyl-γ-D- with (L-alanyl-γ-D- -diaminopimelate containing) alanyl-γ-D-glutamyl-L- glutamyl-meso-2,6- molybdopterin) cys α-D-muramoyl- D-glt dehydrogenase ala UDP-N-acetyl- D-muramoyl- ser a tRNA sec glu a tRNA glu 7-cyano-7-deazaguanine 2-deoxy- -D-ribose 1- ATP dADP pyruvate synthetase]- 6 α synthase QueC: queC TusD:TusE phosphate degradation glutamyl-meso-2,6- glutamyl-meso-2,6- lysyl-D-alanyl-D-alanine) diaminopimeloyl- UDP-N-acetyl- cofactor L-alanine E2 protein] N -D-muramate L-alanine(1-) sulfurtransferase: diaminopimeloyl- diaminopimeloyl-D- D-alanine α-D-muramate chaperone]- L-tyrosine -dihydrolipoyl- ser Ala asp α penicillin-binding RS05755 RS01630 ser a tRNA a tRNA ala tRNA asp preQ AVM72_RS08485 2-deoxy- -D- NADH-quinone dihydrolipoyl RS09540 glutamate- elongator 0 D-alanyl-D-alanine) alanine) tetrapeptide penicillin-binding L-cysteine L-lysine 1,6-anhydro-N- lys a tRNA Lys tyr a tRNA Tyr his a tRNA His pro a tRNA Pro cys a tRNA Cys met initiator tRNA Met met leu a tRNA Leu arg a tRNA Arg trp a tRNA Trp asn tRNA Asn thr a tRNA Thr ile a tRNA Ile gly a tRNA Gly phe a tRNA Phe a [TusE sulfur UDP-glucose-- ribose 1-phosphate protein 2: mrdA oxidoreductase: UDP-N- dehydrogenase: UDP-N- serine- -tRNA tRNA Met UDP-glucose pentapeptide protein 2: mrdA bifunctional [glutamate- acetylmuramyl- RS09545 Val hexose-1-phosphate D-alanyl-D-alanine UDP-N- acetylmuramoyl- pyruvate acetylmuramate- -tRNA val a tRNA 34 carrier protein]-S 4-epimerase phosphopentomutase: nuoN nuoK lpdA ligase: gltX gln Gln a uridine in tRNA acetylmuramate:L- -ammonia ligase]- L-alanine-- kinase: pyk -L-alanine L-alanine ligase: serine- alanine- aspartate- a tRNA -sulfanylcysteine uridylyltransferase: GalE: galE carboxypeptidase/ D-alanyl-D-alanine AVM72_RS11705 cysteine dihydrolipoyl Metabolic Regulator AVM72_RS03725 alanyl-gamma-D- adenylyl-L-tyrosine D-glutamate ligase: murC amidase serS lysine- tyrosine-- histidine- glutamate-- proline-- -tRNA -tRNA -tRNA cysteine-- methionine- methionine- leucine-- arginine-- tryptophan- asparagine- threonine- isoleucine- glycine--tRNA phenylalanine- AVM72_RS01490 penicillin-binding D-alanyl-D-alanine- carboxypeptidase/ nuoI nuoH desulfurase: dehydrogenase: RS06705 RS12280 Biosynthesis α-D-glucopyranose 2-deoxy-D-ribose glutamyl- meso- phosphorylase/ ligase: murD an [apo BCAA AmpD: ampD -tRNA tRNA ligase: -tRNA tRNA ligase: tRNA ligase: valine--tRNA ligase: ligase: ligase: ligase: tRNA ligase: -tRNA -tRNA tRNA ligase: tRNA ligase: -tRNA -tRNA -tRNA -tRNA ligase: glyQ -tRNA ligase: tRNA 2- UDP-α-D-galactose protein 2: endopeptidase: dacB D-alanyl-D-alanine- AVM72_RS11720 AVM72_RS04815 AVM72_RS04655 RS09385 1-phosphate 5-phosphate diaminopimelate [glutamate-- dehydrogenase RS09335 ligase: lysS AVM72_RS00285 ligase: hisS AVM72_RS05810 AVM72_RS02545 AVM72_RS03075 serS alaS aspS AVM72_RS05805 ligase: metG ligase: metG AVM72_RS11000 AVM72_RS11060 ligase: trpS ligase: asnS ligase: thrS ligase: ileS AVM72_RS12570 pheS pheT ppGpp metabolism thiouridine(34) AVM72_RS12915 endopeptidase: dacB nuoF IscS subfamily pyruvate UDP-N-acetyl- ligase: mpl ammonia-ligase] dATP E2 protein] N 6 α N-acetyl-D- an L-seryl- synthase [+ 3 isozymes] a peptidoglycan with AVM72_RS11735 cysteine UDP-N-acetyl- -D-muramoyl- sec an L-methionyl- phosphomannomutase/ deoxyribose- adenylyltransferase: -lipoyl-L-lysine [tRNA ] an L-lysyl- an L-tyrosyl- an
Recommended publications
  • | Hai Lui a Un Acutul Luniit Moonhiti
    |HAI LUI AUN ACUTULUS010006055B2 LUNIIT MOONHITI (12 ) United States Patent (10 ) Patent No. : US 10 , 006 , 055 B2 Burk et al. (45 ) Date of Patent: Jun . 26 , 2018 ( 54 ) MICROORGANISMS FOR PRODUCING 2002/ 0168654 A1 11/ 2002 Maranas et al. 2003 / 0059792 Al 3 /2003 Palsson et al . BUTADIENE AND METHODS RELATED 2003 /0087381 A1 5 / 2003 Gokarn THERETO 2003 / 0224363 Al 12 /2003 Park et al . 2003 / 0233218 Al 12 /2003 Schilling (71 ) Applicant: Genomatica , Inc. , San Diego , CA (US ) 2004 / 0009466 AL 1 /2004 Maranas et al. 2004 / 0029149 Al 2 /2004 Palsson et al. ( 72 ) Inventors : Mark J . Burk , San Diego , CA (US ) ; 2004 / 0072723 A1 4 /2004 Palsson et al. Anthony P . Burgard , Bellefonte , PA 2004 / 0152159 Al 8 / 2004 Causey et al . 2005 /0042736 A1 2 / 2005 San et al . (US ) ; Robin E . Osterhout , San Diego , 2005 / 0079482 A1 4 / 2005 Maranas et al . CA (US ) ; Jun Sun , San Diego , CA 2006 / 0046288 Al 3 / 2006 Ka - Yiu et al. ( US ) ; Priti Pharkya , San Diego , CA 2006 / 0073577 A1 4 / 2006 Ka - Yiu et al . (US ) 2007 /0184539 Al 8 / 2007 San et al . 2009 / 0047718 Al 2 / 2009 Blaschek et al . 2009 / 0047719 Al 2 / 2009 Burgard et al . (73 ) Assignee : Genomatica , Inc ., San Diego , CA (US ) 2009 /0191593 A1 7 / 2009 Burk et al . 2010 / 0003716 A1 1 / 2010 Cervin et al. ( * ) Notice : Subject to any disclaimer , the term of this 2010 /0184171 Al 7 /2010 Jantama et al. patent is extended or adjusted under 35 2010 /0304453 Al 12 / 2010 Trawick et al .
    [Show full text]
  • (12) Patent Application Publication (10) Pub. No.: US 2014/0155567 A1 Burk Et Al
    US 2014O155567A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2014/0155567 A1 Burk et al. (43) Pub. Date: Jun. 5, 2014 (54) MICROORGANISMS AND METHODS FOR (60) Provisional application No. 61/331,812, filed on May THE BIOSYNTHESIS OF BUTADENE 5, 2010. (71) Applicant: Genomatica, Inc., San Diego, CA (US) Publication Classification (72) Inventors: Mark J. Burk, San Diego, CA (US); (51) Int. Cl. Anthony P. Burgard, Bellefonte, PA CI2P 5/02 (2006.01) (US); Jun Sun, San Diego, CA (US); CSF 36/06 (2006.01) Robin E. Osterhout, San Diego, CA CD7C II/6 (2006.01) (US); Priti Pharkya, San Diego, CA (52) U.S. Cl. (US) CPC ................. CI2P5/026 (2013.01); C07C II/I6 (2013.01); C08F 136/06 (2013.01) (73) Assignee: Genomatica, Inc., San Diego, CA (US) USPC ... 526/335; 435/252.3:435/167; 435/254.2: (21) Appl. No.: 14/059,131 435/254.11: 435/252.33: 435/254.21:585/16 (22) Filed: Oct. 21, 2013 (57) ABSTRACT O O The invention provides non-naturally occurring microbial Related U.S. Application Data organisms having a butadiene pathway. The invention addi (63) Continuation of application No. 13/101,046, filed on tionally provides methods of using Such organisms to produce May 4, 2011, now Pat. No. 8,580,543. butadiene. Patent Application Publication Jun. 5, 2014 Sheet 1 of 4 US 2014/O155567 A1 ?ueudos!SMS |?un61– Patent Application Publication Jun. 5, 2014 Sheet 2 of 4 US 2014/O155567 A1 VOJ OO O Z?un61– Patent Application Publication US 2014/O155567 A1 {}}} Hººso Patent Application Publication Jun.
    [Show full text]
  • Supplementary Informations SI2. Supplementary Table 1
    Supplementary Informations SI2. Supplementary Table 1. M9, soil, and rhizosphere media composition. LB in Compound Name Exchange Reaction LB in soil LBin M9 rhizosphere H2O EX_cpd00001_e0 -15 -15 -10 O2 EX_cpd00007_e0 -15 -15 -10 Phosphate EX_cpd00009_e0 -15 -15 -10 CO2 EX_cpd00011_e0 -15 -15 0 Ammonia EX_cpd00013_e0 -7.5 -7.5 -10 L-glutamate EX_cpd00023_e0 0 -0.0283302 0 D-glucose EX_cpd00027_e0 -0.61972444 -0.04098397 0 Mn2 EX_cpd00030_e0 -15 -15 -10 Glycine EX_cpd00033_e0 -0.0068175 -0.00693094 0 Zn2 EX_cpd00034_e0 -15 -15 -10 L-alanine EX_cpd00035_e0 -0.02780553 -0.00823049 0 Succinate EX_cpd00036_e0 -0.0056245 -0.12240603 0 L-lysine EX_cpd00039_e0 0 -10 0 L-aspartate EX_cpd00041_e0 0 -0.03205557 0 Sulfate EX_cpd00048_e0 -15 -15 -10 L-arginine EX_cpd00051_e0 -0.0068175 -0.00948672 0 L-serine EX_cpd00054_e0 0 -0.01004986 0 Cu2+ EX_cpd00058_e0 -15 -15 -10 Ca2+ EX_cpd00063_e0 -15 -100 -10 L-ornithine EX_cpd00064_e0 -0.0068175 -0.00831712 0 H+ EX_cpd00067_e0 -15 -15 -10 L-tyrosine EX_cpd00069_e0 -0.0068175 -0.00233919 0 Sucrose EX_cpd00076_e0 0 -0.02049199 0 L-cysteine EX_cpd00084_e0 -0.0068175 0 0 Cl- EX_cpd00099_e0 -15 -15 -10 Glycerol EX_cpd00100_e0 0 0 -10 Biotin EX_cpd00104_e0 -15 -15 0 D-ribose EX_cpd00105_e0 -0.01862144 0 0 L-leucine EX_cpd00107_e0 -0.03596182 -0.00303228 0 D-galactose EX_cpd00108_e0 -0.25290619 -0.18317325 0 L-histidine EX_cpd00119_e0 -0.0068175 -0.00506825 0 L-proline EX_cpd00129_e0 -0.01102953 0 0 L-malate EX_cpd00130_e0 -0.03649016 -0.79413596 0 D-mannose EX_cpd00138_e0 -0.2540567 -0.05436649 0 Co2 EX_cpd00149_e0
    [Show full text]
  • Generated by SRI International Pathway Tools Version 25.0, Authors S
    Authors: Pallavi Subhraveti Ron Caspi Peter Midford Peter D Karp An online version of this diagram is available at BioCyc.org. Biosynthetic pathways are positioned in the left of the cytoplasm, degradative pathways on the right, and reactions not assigned to any pathway are in the far right of the cytoplasm. Transporters and membrane proteins are shown on the membrane. Ingrid Keseler Periplasmic (where appropriate) and extracellular reactions and proteins may also be shown. Pathways are colored according to their cellular function. Gcf_000753795Cyc: Shewanella mangrovi YQH10 Cellular Overview Connections between pathways are omitted for legibility. Anamika Kothari molybdate phosphate phosphate PstC RS04785 RS08110 FtsX GspE RS18465 FliL RS02695 RS05740 ModC RsxB RS12030 SohB FliG FliM FliQ FlhF RS02410 RS02250 RS10010 RS15620 LptG RS01680 RS01605 MurJ RS02400 RS01330 RS11775 RS06520 RS11750 RS08505 FlhB RS00580 RS09545 LptC CrcB RS06405 RS14070 RS14040 FliG RS08485 RS08495 RS00745 RS15365 RS01080 MotA RS11785 RS09655 CcmD RS19200 YajC BrnQ TrkA ArsB RS02180 RS05465 NrfE FlhB FliO FliJ FliF TolR RS10365 ZipA RS06935 RS05785 RS12390 GspL RS03340 RS03595 RS06070 RS07340 RS16385 UbiB PstB PstB molybdate phosphate phosphate LolA RS14075 6 Tetrapyrrole Biosynthesis N -(3-methylbut- ditrans,octacis- a peptidoglycan with 3-phenyl-2- ditrans,octacis- ditrans,octacis- a [bis(guanylyl UDP-N-acetyl- (4R)-4-hydroxy- a [protein]-L- a [protein]-L- a [protein] Cofactor, Carrier, and Vitamin Biosynthesis a sulfurated a lipid II MoO - a uracil in DNA a
    [Show full text]
  • Supplemental Figure S1. Principal Component Analysis (PCA) for the Leaf and Root Transcriptomes
    Supplemental Figure S1. Principal component analysis (PCA) for the leaf and root transcriptomes. A ZT12 ZT18 ZT0 ZT6 ZT12 ZT18 ZT0 ZT6 → → → Pattern 1 ↗ ↘ ↗ ↘ ↘ ↘ ↘ → → → Pattern 2 ↗ ↘ ↗ ↘ ↘ ↘ ↘ → → → → Pattern 3 ↗ ↘ ↗ ↘ ↘ ↘ ↘ → → → → Pattern 4 ↘ ↗ ↘ ↘ ↘ ↘ ↘ ↗ → ↗ Pattern 5 ↗ ↘ ↗ ↘ → ↘ → → ↗ → ↗ Pattern 6 ↗ ↘ ↗ ↘ → ↘ → → ↗ → Pattern 7 ↘ ↗ ↘ ↗ ↘ → ↘ ↗ → ↗ → Pattern 8 ↘ ↗ ↘ → ↘ → ↘ ↗ ↗ ↗ ↗ Pattern 9 ↗ ↘ ↗ → → → → ↗ ↗ ↗ Pattern 10 ↘ ↗ ↘ ↗ → → → ↗ ↗ ↗ Pattern 11 ↘ ↗ ↘ ↗ → → → ↗ ↗ ↗ ↗ Pattern 12 ↘ ↗ ↘ → → → → Supplemental Figure S2. The 12 different diurnal patterns set for this study (A) and gene expression variations in the leaves (B) and roots (C). (B, C) The shaded areas show nighttime. The data points indicate the average of expression levels of five replicates. Figure S2 continued B Leaf - Pattern 1 Leaf - Pattern 2 Leaf - Pattern 3 400 2500 1200 350 1000 2000 300 800 250 1500 200 600 1000 150 400 100 Expression Level Level (TPM) Expression Expression Level Level Expression (TPM) 500 Expression Level Level (TPM) Expression 200 50 0 0 0 12 18 0 6 12 18 0 6 12 18 0 6 12 18 0 6 12 18 0 6 12 18 0 6 ZT ZT ZT Leaf - Pattern 4 Leaf - Pattern 5 Leaf - Pattern 6 3000 6000 20000 18000 2500 5000 16000 14000 2000 4000 12000 1500 3000 10000 8000 1000 2000 6000 Expression Level Level (TPM) Expression 4000 Expression Level Level Expression (TPM) 500 Level Expression (TPM) 1000 2000 0 0 0 12 18 0 6 12 18 0 6 12 18 0 6 12 18 0 6 12 18 0 6 12 18 0 6 ZT ZT ZT Leaf - Pattern 7 Leaf - Pattern 8 Leaf - Pattern 9 4500 400 2500 4000 350 2000 3500 300 3000 250
    [Show full text]
  • R Graphics Output
    Figure S1. Multidimensional scaling analysis of the RNA-seq experiments. Samples are projected on the two first dimensions according to their gene expression profiles. Closeness between samples on the grid indicates a strong similarity. Figure S2. Similar tissue type are strongly correlated. Spearman's rho correlation was measured to check biological replicate homogeneity. Higher rho values indicate stronger similarities between pairs of samples. −log10(Pval) ● 5● 10● 15● 20 OL vs AR YL vs OL YL+YS+OL vs AR copper ion transport ● microtubule−based movement ● cyanate catabolic process ● establishment of protein localization ● DNA unwinding involved in DNA replication ● intracellular distribution of mitochondria ● regulation of root development ● DNA methylation on cytosine within a CG sequence ● carbon utilization ● glutamine biosynthetic process ● maintenance of DNA methylation ● photosystem II assembly ● response to singlet oxygen ● DNA replication initiation ● chlorophyll biosynthetic process ● specification of plant organ axis polarity ● mitotic cell cycle ● reductive pentose−phosphate cycle ● cellular response to nitrogen starvation ● double−strand break repair via homologous recombination ● photosynthesis, light harvesting in photosystem I ● cellular manganese ion homeostasis ● mitotic cell cycle phase transition ● protein−chromophore linkage ● cellular zinc ion homeostasis ● regulation of cyclin−dependent protein serine/threonine kinase activity ● response to light stimulus ● recognition of pollen ● cell division ● photosynthesis
    [Show full text]
  • All Enzymes in BRENDA™ the Comprehensive Enzyme Information System
    All enzymes in BRENDA™ The Comprehensive Enzyme Information System http://www.brenda-enzymes.org/index.php4?page=information/all_enzymes.php4 1.1.1.1 alcohol dehydrogenase 1.1.1.B1 D-arabitol-phosphate dehydrogenase 1.1.1.2 alcohol dehydrogenase (NADP+) 1.1.1.B3 (S)-specific secondary alcohol dehydrogenase 1.1.1.3 homoserine dehydrogenase 1.1.1.B4 (R)-specific secondary alcohol dehydrogenase 1.1.1.4 (R,R)-butanediol dehydrogenase 1.1.1.5 acetoin dehydrogenase 1.1.1.B5 NADP-retinol dehydrogenase 1.1.1.6 glycerol dehydrogenase 1.1.1.7 propanediol-phosphate dehydrogenase 1.1.1.8 glycerol-3-phosphate dehydrogenase (NAD+) 1.1.1.9 D-xylulose reductase 1.1.1.10 L-xylulose reductase 1.1.1.11 D-arabinitol 4-dehydrogenase 1.1.1.12 L-arabinitol 4-dehydrogenase 1.1.1.13 L-arabinitol 2-dehydrogenase 1.1.1.14 L-iditol 2-dehydrogenase 1.1.1.15 D-iditol 2-dehydrogenase 1.1.1.16 galactitol 2-dehydrogenase 1.1.1.17 mannitol-1-phosphate 5-dehydrogenase 1.1.1.18 inositol 2-dehydrogenase 1.1.1.19 glucuronate reductase 1.1.1.20 glucuronolactone reductase 1.1.1.21 aldehyde reductase 1.1.1.22 UDP-glucose 6-dehydrogenase 1.1.1.23 histidinol dehydrogenase 1.1.1.24 quinate dehydrogenase 1.1.1.25 shikimate dehydrogenase 1.1.1.26 glyoxylate reductase 1.1.1.27 L-lactate dehydrogenase 1.1.1.28 D-lactate dehydrogenase 1.1.1.29 glycerate dehydrogenase 1.1.1.30 3-hydroxybutyrate dehydrogenase 1.1.1.31 3-hydroxyisobutyrate dehydrogenase 1.1.1.32 mevaldate reductase 1.1.1.33 mevaldate reductase (NADPH) 1.1.1.34 hydroxymethylglutaryl-CoA reductase (NADPH) 1.1.1.35 3-hydroxyacyl-CoA
    [Show full text]
  • Non-Natural Microbial Organisms with Improved
    (19) *EP003194604B1* (11) EP 3 194 604 B1 (12) EUROPEAN PATENT SPECIFICATION (45) Date of publication and mention (51) Int Cl.: of the grant of the patent: C12P 7/42 (2006.01) C12P 7/16 (2006.01) 26.02.2020 Bulletin 2020/09 (86) International application number: (21) Application number: 15775307.0 PCT/US2015/050923 (22) Date of filing: 18.09.2015 (87) International publication number: WO 2016/044713 (24.03.2016 Gazette 2016/12) (54) NON-NATURAL MICROBIAL ORGANISMS WITH IMPROVED ENERGETIC EFFICIENCY NICHT-NATÜRLICHE MIKROBIELLE ORGANISMEN MIT VERBESSERTER ENERGIEEFFIZIENZ ORGANISMES MICROBIENS NON NATURELS PRÉSENTANT UNE MEILLEURE EFFICACITÉ ÉNERGÉTIQUE (84) Designated Contracting States: • V. Monedero ET AL: "Mutations lowering the AL AT BE BG CH CY CZ DE DK EE ES FI FR GB phosphatase activity of HPr kinase/phosphatase GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO switch off carbon metabolism.", The EMBO PL PT RO RS SE SI SK SM TR journal, vol. 20, no. 15 1 August 2001 (2001-08-01), 1 August 2001 (2001-08-01), pages 3928-3937, (30) Priority: 18.09.2014 US 201462052341 P XP055233568, Retrieved from the Internet: URL:http://emboj.embopress.org/content/20/ (43) Date of publication of application: 15/3928.full.pdf [retrieved on 2015-12-03] 26.07.2017 Bulletin 2017/30 • MARTA PAPINI ET AL: "Physiological characterization of recombinant Saccharomyces (73) Proprietor: Genomatica, Inc. cerevisiae expressing the phosphoketolase San Diego, CA 92121 (US) pathway: validation of activity through 13C-based metabolic flux analysis", APPLIED (72) Inventors: MICROBIOLOGY AND BIOTECHNOLOGY, • PHARKYA, Priti SPRINGER, BERLIN, DE, vol.
    [Show full text]
  • (12) United States Patent (10) Patent No.: US 9,169,486 B2 Burk Et Al
    US009 1694.86B2 (12) United States Patent (10) Patent No.: US 9,169,486 B2 Burk et al. (45) Date of Patent: Oct. 27, 2015 (54) MICROORGANISMS FOR PRODUCING 2003, OO87381 A1 5/2003 Gokarn BUTADIENE AND METHODS RELATED 2003,0224363 A1 12/2003 Park et al. THERETO 2003/0233218 A1 12/2003 Schilling 2004/OOO9466 A1 1/2004 Maranas et al. (75) Inventors: Mark J. Burk, San Diego, CA (US); 3.92. !: A. 3.38: Eas al Anthony Burgard Bellefonte, PA 2004/0152159 A1 8/2004 CauseyaSSO etca. al. (US); Robin E. Osterhout, San Diego, 2005/0042736 A1 2/2005 San et al. CA (US); Jun Sun, San Diego, CA (US); 2005, 0079482 A1 4/2005 Maranas et al. Priti Pharkya, San Diego, CA (US) 2006/004.6288 A1 3/2006 Ka-Yiu et al. 2006, OO73577 A1 4/2006 Ka-Yiu et al. (73) Assignee: Genomatica, Inc., San Diego, CA (US) 2009/00477182007/O184539 A1 2/20098, 2007 SanBlaschek et al. et al. (*) Notice: Subject to any disclaimer, the term of this 39887. A. 23. Ewsi al. patent is extended or adjusted under 35 2010.0003716 A1 1/2010 Cervin et al. U.S.C. 154(b) by 0 days. 2010.0184171 A1 7, 2010 Jantama et al. 2010/0304453 A1 12/2010 Trawicket al. 2010/0330635 Al 12/2010 Burgard et al. (21) Appl. No.: 13/527,440 2011/0008861 A1 1/2011 Berry et al. 2011/0300597 A1* 12/2011 Burk et al. .................... 435/167 (22) Filed: Jun. 19, 2012 2012/0225466 A1 9, 2012 Burk et al.
    [Show full text]
  • (12) Patent Application Publication (10) Pub. No.: US 2015/0240226A1 Mathur Et Al
    US 20150240226A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2015/0240226A1 Mathur et al. (43) Pub. Date: Aug. 27, 2015 (54) NUCLEICACIDS AND PROTEINS AND CI2N 9/16 (2006.01) METHODS FOR MAKING AND USING THEMI CI2N 9/02 (2006.01) CI2N 9/78 (2006.01) (71) Applicant: BP Corporation North America Inc., CI2N 9/12 (2006.01) Naperville, IL (US) CI2N 9/24 (2006.01) CI2O 1/02 (2006.01) (72) Inventors: Eric J. Mathur, San Diego, CA (US); CI2N 9/42 (2006.01) Cathy Chang, San Marcos, CA (US) (52) U.S. Cl. CPC. CI2N 9/88 (2013.01); C12O 1/02 (2013.01); (21) Appl. No.: 14/630,006 CI2O I/04 (2013.01): CI2N 9/80 (2013.01); CI2N 9/241.1 (2013.01); C12N 9/0065 (22) Filed: Feb. 24, 2015 (2013.01); C12N 9/2437 (2013.01); C12N 9/14 Related U.S. Application Data (2013.01); C12N 9/16 (2013.01); C12N 9/0061 (2013.01); C12N 9/78 (2013.01); C12N 9/0071 (62) Division of application No. 13/400,365, filed on Feb. (2013.01); C12N 9/1241 (2013.01): CI2N 20, 2012, now Pat. No. 8,962,800, which is a division 9/2482 (2013.01); C07K 2/00 (2013.01); C12Y of application No. 1 1/817,403, filed on May 7, 2008, 305/01004 (2013.01); C12Y 1 1 1/01016 now Pat. No. 8,119,385, filed as application No. PCT/ (2013.01); C12Y302/01004 (2013.01); C12Y US2006/007642 on Mar. 3, 2006.
    [Show full text]
  • ABBREVIATION NAME ORF 3M2OBLOXRD 3-Methyl-2
    ABBREVIATION NAME ORF 3-Methyl-2-oxobutanoate:lipoamide oxidoreductase(decarboxylating and acceptor- 3M2OBLOXRD 2-methylpropanoylating) ( SA1348 and SA1347 ) 3-Methyl-2-oxopentanoate:lipoamide oxidoreductase(decarboxylating and acceptor- 3M2OPLOXRD 2-methylpropanoylating) ( SA1348 and SA1347 ) 4-Methyl-2-oxopentanoate:lipoamide oxidoreductase(decarboxylating and acceptor- 4M2OPLOXRD 2-methylpropanoylating) ( SA1348 and SA1347 ) 6PGALSZ 6-phospho-beta-galactosidase SA1991 6PHBG 6-phospho-beta-glucosidase SA0256 ABTAr 4-aminobutyrate transaminase SA2397 ACACT1r acetyl-CoA C-acetyltransferase ( SA0342 or ( SA0223 or SA0534 ) ) ACACT2r acetyl-CoA C-acyltransferase (butanoyl-CoA) (r) ( SA0342 or ( SA0223 or SA0534 ) ) ACACT3r acetyl-CoA C-acyltransferase (hexanoyl-CoA) (r) ( SA0223 or SA0534 ) ACACT4r acetyl-CoA C-acyltransferase (octanoyl-CoA) (r) ( SA0223 or SA0534 ) ACACT5r acetyl-CoA C-acyltransferase (decanoyl-CoA) (r) ( SA0223 or SA0534 ) ACACT6r acetyl-CoA C-acyltransferase (dodecanoyl-CoA) (r) ( SA0223 or SA0534 ) ACACT7r acetyl-CoA C-acyltransferase (tetradecanoyl-CoA) (r) ( SA0223 or SA0534 ) ACALDi acetaldehyde dehydrogenase (acetylating) SA0143 ACCOAC acetyl-CoA carboxylase ( SA1522 and ( SA1435 or SA1358 ) and ( SA1357 or SA1434 ) and SA1523 ) ACGApts N-Acetyl-D-glucosamine transport via PEP:Pyr PTS SA1547 ACGK acetylglutamate kinase SA0176 ACGS N-acetylglutamate synthase SA0177 ACHBS 2-aceto-2-hydroxybutanoate synthase ( ( SA1859 or SA2008 ) and SA1860 ) ACKr acetate kinase SA1533 ACLDC acetolactate decarboxylase ( SA2394 or SA2007
    [Show full text]
  • Generate Metabolic Map Poster
    Authors: Pallavi Subhraveti Ron Caspi Peter Midford Peter D Karp An online version of this diagram is available at BioCyc.org. Biosynthetic pathways are positioned in the left of the cytoplasm, degradative pathways on the right, and reactions not assigned to any pathway are in the far right of the cytoplasm. Transporters and membrane proteins are shown on the membrane. Ingrid Keseler Periplasmic (where appropriate) and extracellular reactions and proteins may also be shown. Pathways are colored according to their cellular function. Gcf_000091785Cyc: Legionella longbeachae NSW150 Cellular Overview Connections between pathways are omitted for legibility. Anamika Kothari sn-glycerol spermidine 3-phosphate putrescine a sulfonate nitrate hydrogencarbonate predicted predicted ABC ABC transporter transporter RS16610 of sn- of spermidine/ glycerol 3- putrescine phosphate a sulfonate nitrate spermidine hydrogencarbonate putrescine sn-glycerol 3-phosphate Amino Acid Degradation Amine and Polyamine Biosynthesis Hormone Biosynthesis Aldehyde Degradation glutaminyl-tRNA gln Aminoacyl-tRNA Charging N 6 -(3-methylbut- a 1-palmitoyl-2- L-alanyl-γ-D- L-alanyl-γ-D- a [bis(guanylyl a [protein] biosynthesis via transamidation core a peptide with homospermidine homospermidine indole-3-acetate L-leucine degradation I a sulfurated 2-en-1-yl)- acyl-sn-glycerol glutamyl-meso-2,6- glutamyl-meso- UDP-N-acetyl- a [glutamine- γ-L-glutamyl- Polyprenyl Biosynthesis L-proline degradation I L-tyrosine degradation I methylglyoxal degradation I oligosaccharide- ATP molybdopterin) cys a type IV prepilin gly an N-terminal C-terminal glu biosynthesis II L-arginine degradation [sulfur carrier] 37 synthetase]- ATP biosynthesis I biosynthesis TCA cycle TCA cycle I (prokaryotic) adenosine lipid A (E.
    [Show full text]