Generated by SRI International Pathway Tools Version 25.0, Authors S

Total Page:16

File Type:pdf, Size:1020Kb

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_001431645Cyc: Stenotrophomonas panacihumi JCM 16536 Cellular Overview Connections between pathways are omitted for legibility. Anamika Kothari molybdate spermidine ammonium phosphate putrescine RS01245 RS09040 RS02020 RS09210 RS06445 ModC RS13295 RS07950 RS10935 RS05290 CcmE RS10150 RS15175 CcmA TatC RS15730 PotA FliR FliN FliF RS16780 RS13205 RS11350 RS08505 RS08615 RS04655 HtpX MreD RodA RS11935 SecA Amt RS14010 RS09060 RS11475 FliJ FtsE Cls FtsY SecF RS04370 RS14605 RS03760 RS08055 RS10260 RS10235 RS11315 RarD RS07635 RS12840 RS06270 RS15230 MurJ RS07085 RS02925 FlhA RS06365 AmpE MgtE RS05150 RS17505 PstB spermidine molybdate ammonium putrescine phosphate RS11800 FliD Cofactor, Carrier, and Vitamin Biosynthesis Amino Acid Degradation Aromatic Compound Macromolecule Modification tRNA-uridine 2-thiolation NADH repair (prokaryotes) Degradation di-trans,octa-cis UDP-N-acetyl- ditrans,octacis- a peptidoglycan with UDP-N-acetyl-α-D- L-alanyl-γ-D- an N-terminal- an N-terminal- a peptidoglycan (R)-4-hydroxy- 4-hydroxy- a peptide with a [protein] and selenation (bacteria) ditrans,octacis- ditrans,octacis- phosphoenol an L-asparaginyl- [2Fe-2S] iron-sulfur Tetrapyrrole Biosynthesis L-valine degradation I -undecaprenyl α-D-muramoyl- undecaprenyldiphospho- (L-alanyl-γ-D-glutamyl- muramoyl-L-alanyl- undecaprenyldiphospho- undecaprenyldiphospho- glutamyl-meso- UDP-N-acetyl- a [glutamine- L-methionyl-L- L-methionyl-L- dimer (meso- 4-methyl-2- 4-methyl-2- an N-terminal C-terminal glu ubiquinol-8 biosynthesis ubiquinol-8 biosynthesis superpathway of tetrahydrofolate biosynthesis flavin biosynthesis I (bacteria and plants) superpathway of coenzyme A biosynthesis I (bacteria) NAD de novo biosynthesis superpathway of adenosylcobalamin salvage from cobinamide I adenosylcobalamin 2-methyladeninyl adenosylcobamide L-isoleucine degradation I L-leucine degradation I L-histidine degradation II L-phenylalanine catechol ATP dGDP pyruvate [tRNA Asn ] cluster biosynthesis phosphate L-alanyl-γ-D- N-acetyl-(N-acetyl-β-D- L-lysyl-D-alanyl-D- γ-D-glutamyl-meso- diaminopimelate α-D-muramate synthetase]- cysteinyl-[protein] threonyl-[protein] diaminopimelate oxoglutarate oxoglutarate L-methionine L-glutamate RS00630 FlgK (late decarboxylation) (early decarboxylation) II (from tryptophan) salvage from cobalamin biosynthesis from adenosylcobinamide-GDP NADH degradation degradation I (meta D-alanyl-D-alanine N-acetyl-(N- N-acetyl-(N- putative 4- putative 4- cys glutamyl-meso-2,6- glucosaminyl)muramoyl- alanine) pentapeptide 2,6-diaminopimelate L-tyrosine containing) 3-methyl-2- a 5,10- superpathway of heme b val I (aerobic) -cleavage pathway) acetylglucosaminyl) acetylglucosaminyl) hydroxy-4-methyl- hydroxy-4-methyl- L-cysteine desulfurase all-trans- cob(II)inamide heme b biosynthesis II Polyprenyl Biosynthesis ile his diaminopimeloyl- L-alanyl-γ-D-glutamyl-L- γ chorismate GTP oxobutanoate methylenetetrahydrofolate trp cob(I)alamin 2-methyladenine biosynthesis from glutamate cysteine leu muramoyl-L-alanyl- - muramoyl-L-alanyl- UDP-N- type I methionyl type I methionyl 2-oxoglutarate 2-oxoglutarate type I methionyl 30S aminoacyl- 4-hydroxybenzoate octaprenyl GTP (oxygen-independent) catechol D-alanyl-D-alanine lysyl-D-alanyl-D-alanine β γ tryptophan 2,3- cob(I)yrinic acid a,c-diamide desulfurase: branched-chain branched-chain histidine phe UDP-N- D-isoglutaminyl-N-( - -D-isoglutaminyl- acetylmuramate:L- bifunctional [glutamate- aminopeptidase: aminopeptidase: pyruvate penicillin- aldolase: aldolase: aminopeptidase: ribosomal tRNA cysteine diphosphate branched-chain β 3-methyl-2-oxobutanoate dioxygenase: adenosyltransferase: cobO nicotinate-nucleotide-- glu polyisoprenoid biosynthesis (E. coli) ARC20_RS02445 amino acid amino acid ammonia- phenylalanine 4- phospho-N- acetylmuramoyl- D-asparaginyl)-L-lysyl- N-( -D-asparaginyl) alanyl-gamma-D- -ammonia ligase]- map map kinase: pyk binding ARC20_RS05905 ARC20_RS05905 map protein hydrolase: RS00650 FlgL desulfurase: GTP GTP uroporphyrinogen-III amino acid 4-hydroxybenzoate hydroxymethyltransferase: ARC20_RS10940 cob(I)yrinic acid a,c-diamide dimethylbenzimidazole glutamate- an [L-cysteine aminotransferase: aminotransferase: lyase: hutH monooxygenase: acetylmuramoyl- monofunctional tripeptide--D-alanyl- D-alanyl-D-alanine -L-lysyl-D-alanine glutamyl- meso- adenylyl-L-tyrosine type I methionyl type I methionyl protein type I methionyl S6--L- pth ARC20_RS02445 all-trans- cyclohydrolase cyclohydrolase N-Formyl-L- cob(II)alamin uroporphyrinogen (R)-NADHX aminotransferase: urocanate 4-carboxy-4- 4-carboxy-4- octaprenyltransferase: panB adenosyltransferase: phosphoribosyltransferase: -tRNA desulfurase]-S- ARC20_RS05925 ARC20_RS05925 ARC20_RS02715 HMS pentapeptide- biosynthetic D- alanine ligase: diaminopimelate phosphorylase/ aminopeptidase: aminopeptidase: 2: mrdA aminopeptidase: glutamate 4-hydroxybenzoate octaprenyl I FolE: folE II RibA: ribA kynurenine decarboxylase: IPP bifunctional ARC20_RS05925 4-methyl-2- tyr hydroxy-2- hydroxy-2- aminoacyl- an S-sulfanyl-[L- ubiA 2,5-diamino-6- ARC20_RS09900 cob(I)yrinic acid cobT sulfanyl-L-cysteine transferase: peptidoglycan ARC20_RS14040 ligase: mpl [glutamate-- map ligase: rimK diphosphate 7,8- asp an L-glutamyl-ligase: gltX ARC20_RS03955 ADP-dependent 3-methyl-2- oxopentanoate urocanate monofunctional monofunctional map pyruvate oxoadipate oxoadipate map tRNA cysteine desulfurase] (5-phospho-D- a,c-diamide (3S)-3-methyl-2- HmsH protein: ARC20_RS14035 transglycosylase: ammonia-ligase] dGTP dihydroneopterin Glu coproporphyrinogen III NAD(P)H-hydrate oxobutanoate hydratase: undecaprenyldiphospho- UMP biosynthetic biosynthetic a peptidoglycan hydrolase: RS11960 RS15645 2-dehydropantoate [corrinoid adenosyltranferase]-cob(II)inamide 2-methyladenine [tRNA ] oxopentanoate ARC20_RS17425 adenylyltransferase: aldolase/ aldolase/ 4-hydroxybenzoate 4-hydroxy-3- 3'-triphosphate ribosylamino) aspartate 1- adenosyltransferase: dehydratase/ ARC20_RS04155 N-acetylmuramoyl-L- mtgA UDP-N-acetyl-α-D- peptidoglycan peptidoglycan UDP-N-acetyl- with D,D cross- D-ala a [protein] C- arfB adenosylcobinamide- ribotide phosphate oxygen-independent (2Z)-2- glnE an N-terminal L- an N-terminal L- oxaloacetate oxaloacetate octaprenyltransferase: octaprenylbenzoate pyrimidin- 2-dehydropantoate decarboxylase: cobO glutamyl-tRNA a [TusA sulfur- NAD(P)H-hydrate 4-imidazolone- alanyl-γ-D-glutamyl-meso muramoyl-L-alanyl- transglycosylase: transglycosylase: α-D-muramoyl- met met links (meso- met a peptide terminal α-L- GDP coproporphyrinogen hydroxypenta- cysteinyl-[protein] threonyl-[protein] decarboxylase: decarboxylase: ubiA 4(3H)-one 2-reductase: panE ARC20_RS06285 L-kynurenine cob(I)yrinic acid reductase: carrier protein]-S- epimerase: 3-methylbutanoyl- 5-propanoate -2,6-diaminopimeloyl- a peptidoglycan with di-trans,octa-cis γ-D-glutamyl-meso- mtgA mtgA L-alanyl-γ-D- diaminopimelate glutamate-α- an S-sulfanyl-[cysteine bifunctional ARC20_RS15810 III oxidase: hemN DMAPP L-glutamine 2,4-dienoate ligK ligK a,c-diamide sulfanyl-L-cysteine ARC20_RS11045 CoA D-alanyl-D-alanine (L-alanyl-γ-D-glutamyl- -undecaprenyl 2,6-diaminopimeloyl- glutamyl-meso-2,6- a [glutamine containing) L-glutamate Asn desulfurase]-[disordered- 7,8- β (S)-NADHX isobutanoyl-CoA (2S)-2- imidazolonepropionase: pyruvate pyruvate asn tRNA RS08440 4-hydroxy-3- diaminohydroxyphosphoribosylaminopyrimidine (R)-pantoate -alanine adenosyltransferase: adenosylcobinamide- (S)-4-amino-5- isovaleryl-CoA degradation II 2-keto-4- diphosphate D-alanyl-D-alanine diaminopimelate synthetase]-O form scaffold dihydroneopterin [corrinoid adenosyltranferase]-cob(I)inamide protoporphyrinogen IX methylbutanoyl-CoA ARC20_RS04170 L-lysyl-D-alanyl-D- a peptidoglycan di-trans,octa-cis a peptidoglycan di-trans,octa-cis octaprenylbenzoate deaminase/5-amino-6-(5-phosphoribosylamino) GDP oxopentanoate pentenoate 4 -(5'-adenylyl) 2-octaprenylphenol 3'-phosphate ARC20_RS09900 bifunctional dehydrogenase: alanine) pentapeptide dimer (E. faeciums) -undecaprenyl dimer (E. faecium -undecaprenyl protein] complex uracil reductase RibD: ribD cob(I)yrinic acid a,c-diamide ribazoletransferase: gln hydratase: -L-tyrosine 4-hydroxy-3- cob(II)alamin- glutamate-1- a [TusD sulfur- ADP-dependent ARC20_RS13130 N-formimino- diphosphate , tetrapeptide) diphosphate 5-amino-6-(5- pantoate--beta- 3-hydroxy- adenosyltransferase: cobO ARC20_RS12250 glutamate ARC20_RS02615 octaprenylbenzoate 2-polyprenylphenol [corrinoid semialdehyde geranyl carrier protein]-S- NAD(P)H-hydrate 3-methylcrotonyl- L-glutamate phospho-D- alanine ligase: L-kynurenine synthase large 2-keto-4- RS05960 5-hydroxylase: ubiH 6-hydroxylase: ubiB cob(I)yrinic acid a,c-diamide adenosyltranferase] 2,1- diphosphate methylacrylyl-CoA (E)-2- CoA 6 ribosylamino)uracil ARC20_RS06290 Coα-[α-(2- sulfanyl-L-cysteine dehydratase/ formimidoylglutamate a ring-opened 7- an O - ditrans,octacis- a [glutamine (3E)-5-chloro-2- an N-terminal- an N-terminal- L-alanyl-γ-D- a [cysteine desulfurase]- 3,4-dihydroxy-
Recommended publications
  • Yeast Genome Gazetteer P35-65
    gazetteer Metabolism 35 tRNA modification mitochondrial transport amino-acid metabolism other tRNA-transcription activities vesicular transport (Golgi network, etc.) nitrogen and sulphur metabolism mRNA synthesis peroxisomal transport nucleotide metabolism mRNA processing (splicing) vacuolar transport phosphate metabolism mRNA processing (5’-end, 3’-end processing extracellular transport carbohydrate metabolism and mRNA degradation) cellular import lipid, fatty-acid and sterol metabolism other mRNA-transcription activities other intracellular-transport activities biosynthesis of vitamins, cofactors and RNA transport prosthetic groups other transcription activities Cellular organization and biogenesis 54 ionic homeostasis organization and biogenesis of cell wall and Protein synthesis 48 plasma membrane Energy 40 ribosomal proteins organization and biogenesis of glycolysis translation (initiation,elongation and cytoskeleton gluconeogenesis termination) organization and biogenesis of endoplasmic pentose-phosphate pathway translational control reticulum and Golgi tricarboxylic-acid pathway tRNA synthetases organization and biogenesis of chromosome respiration other protein-synthesis activities structure fermentation mitochondrial organization and biogenesis metabolism of energy reserves (glycogen Protein destination 49 peroxisomal organization and biogenesis and trehalose) protein folding and stabilization endosomal organization and biogenesis other energy-generation activities protein targeting, sorting and translocation vacuolar and lysosomal
    [Show full text]
  • The Distribution of Trehalase, Sucrase, Α-Amylase, Glucoamylase and Lactase
    Downloaded from Br. J. Nutr. (197z),28, 129 https://www.cambridge.org/core The distribution of trehalase, sucrase, a-amylase, glucoamylase and lactase (8-galactosidase) along the small intestine of five pigs BY J. A. S'I'EVENS" AND D. E. KIDDER . IP address: Departments of Animal Husbandry and Veterinary Medicine, University of Bristol Langfwd House, Lungford, Bristol BSI 8 70U 170.106.40.40 (Received 24 September 1971 - Accepted 30 December 1971) I. Sucrase, trehalase (EC 3.2. I .28), a-amylase (RC 3.2.I. I) and glucoamylase ("-1.4 , on glucan glucohydrolase, BC 3.2.I .3) activities have been measured in the small intestine 25 Sep 2021 at 22:09:31 mucosa of five pigs varying in age from 19-30 weeks. The determinations were made at frequent intervals along the entire length starting 5 x 10-l m from the pylorus. Lactasc (/I-galactosidase, EC 3.2,I .23) has similarly been measured in one pig. 2. All these enzymes were present in the sample obtained from nearest to the pylorus and rose rapidly in the first few metres. 3. Trehalase and lactase were similarly distributed with a peak activity in the proximal quarter of the small intestine, falling to very low levels in the distal half. 4. Sucrase and glucoamylase resembled one another in distribution pattern with a peak , subject to the Cambridge Core terms of use, available at approximately midway along the small intestine, followed by a slight decrease in sucrase activity distally and a rather greater decrease with glucoamylase. 5. a-Amylasc activity, assumed to be duc to adsorhcd pancrcatic enzyme, had no regular pattern of distribution.
    [Show full text]
  • Supplementary Information
    Supplementary information (a) (b) Figure S1. Resistant (a) and sensitive (b) gene scores plotted against subsystems involved in cell regulation. The small circles represent the individual hits and the large circles represent the mean of each subsystem. Each individual score signifies the mean of 12 trials – three biological and four technical. The p-value was calculated as a two-tailed t-test and significance was determined using the Benjamini-Hochberg procedure; false discovery rate was selected to be 0.1. Plots constructed using Pathway Tools, Omics Dashboard. Figure S2. Connectivity map displaying the predicted functional associations between the silver-resistant gene hits; disconnected gene hits not shown. The thicknesses of the lines indicate the degree of confidence prediction for the given interaction, based on fusion, co-occurrence, experimental and co-expression data. Figure produced using STRING (version 10.5) and a medium confidence score (approximate probability) of 0.4. Figure S3. Connectivity map displaying the predicted functional associations between the silver-sensitive gene hits; disconnected gene hits not shown. The thicknesses of the lines indicate the degree of confidence prediction for the given interaction, based on fusion, co-occurrence, experimental and co-expression data. Figure produced using STRING (version 10.5) and a medium confidence score (approximate probability) of 0.4. Figure S4. Metabolic overview of the pathways in Escherichia coli. The pathways involved in silver-resistance are coloured according to respective normalized score. Each individual score represents the mean of 12 trials – three biological and four technical. Amino acid – upward pointing triangle, carbohydrate – square, proteins – diamond, purines – vertical ellipse, cofactor – downward pointing triangle, tRNA – tee, and other – circle.
    [Show full text]
  • GFAT and PFK Genes Show Contrasting Regulation of Chitin
    www.nature.com/scientificreports OPEN GFAT and PFK genes show contrasting regulation of chitin metabolism in Nilaparvata lugens Cai‑Di Xu1,3, Yong‑Kang Liu2,3, Ling‑Yu Qiu2, Sha‑Sha Wang2, Bi‑Ying Pan2, Yan Li2, Shi‑Gui Wang2 & Bin Tang2* Glutamine:fructose‑6‑phosphate aminotransferase (GFAT) and phosphofructokinase (PFK) are enzymes related to chitin metabolism. RNA interference (RNAi) technology was used to explore the role of these two enzyme genes in chitin metabolism. In this study, we found that GFAT and PFK were highly expressed in the wing bud of Nilaparvata lugens and were increased signifcantly during molting. RNAi of GFAT and PFK both caused severe malformation rates and mortality rates in N. lugens. GFAT inhibition also downregulated GFAT, GNPNA, PGM1, PGM2, UAP, CHS1, CHS1a, CHS1b, Cht1-10, and ENGase. PFK inhibition signifcantly downregulated GFAT; upregulated GNPNA, PGM2, UAP, Cht2‑4, Cht6‑7 at 48 h and then downregulated them at 72 h; upregulated Cht5, Cht8, Cht10, and ENGase; downregulated Cht9 at 48 h and then upregulated it at 72 h; and upregulated CHS1, CHS1a, and CHS1b. In conclusion, GFAT and PFK regulated chitin degradation and remodeling by regulating the expression of genes related to the chitin metabolism and exert opposite efects on these genes. These results may be benefcial to develop new chitin synthesis inhibitors for pest control. Chitin is a linear polymer composed of N-acetylglucosamine units connected by β-1, 4-glycoside bonds and is the second most abundant biopolymer in nature. It is widely distributed in fungi, nematodes, and arthropods1. In insects, chitin is a major component of the exoskeleton, trachea, and the peritrophic matrix that lines the midgut epithelium1–4.
    [Show full text]
  • Unraveling the Function of Trehalose Biosynthesis Genes in Lateral Root Development
    Acknowledgement Unraveling the function of trehalose biosynthesis genes in lateral root development Celine DE MAESSCHALCK Master‟s dissertation submitted to obtain the degree of Master of Biochemistry and Biotechnology Major Plant Biotechnology Academic year 2009-2010 Promoter(s): Prof. Dr. Tom Beeckman Scientific supervisor: Drs. Lorena López Department Plant Biotechnology and Genetics VIB - Department Plant Systems Biology II Acknowledgement ACKNOWLEDGEMENTS First I would like to thank Prof. Dr. T. Beeckman for the opportunities to make my Master thesis possible in his Lab. También me gustaría agradecer a Lorena por haber sido tan buena consejera y por la preocupación que siempre ha mostrado. Ella me ha apoyado durante todo el proceso de componer y analizar los informes. I also need to thank the other people in the lab, Gert, Dominique, Boris, Giel, Marlies, Leen, Wei and Maria, who helps me when I had some questions or problems during the pratical work and to motivate me during writing. Daarnaast moet ik mijn medestudenten bedanken: Evy, Isabel, Morgane, Silke, Lynda, Brecht en Wolf, voor de leuke vijf jaar als student. Ook een dankwoordje voor de klimmers, Bram, Kristof en Thomas die steeds luisterden naar mijn avonturen over epjes wegen en zijwortels tellen. Bram wil ik nog eens extra bedanken voor het nalezen en verbeteren van mijn thesis en steeds klaar te staan met nuttige tips and tricks. Thomas zorgde dan weer voor de muzikale noot gedurende mijn thesis. Ook de brugse vrienden en vriendinnen moet ik bedanken: Loesje voor de Girls-talk en er gewoon te zijn wanneer het nodig was, Charlotte voor het leren van mijn eerste zinnetjes spaans, de scouts,….
    [Show full text]
  • Trehalose-Mediated Enhancement of Glycosaminoglycan Degradation in the Lysosomal Storage Disorder Mucopolysaccharidosis III
    Aus dem Institut für Humangenetik der Universität zu Köln Direktorin: Frau Universitätsprofessor Dr. rer. nat. B. Wirth Trehalose-mediated enhancement of glycosaminoglycan degradation in the lysosomal storage disorder Mucopolysaccharidosis III Trehalose vermittelte Steigerung des Glykosaminoglykan-Abbaus in der lysosomalen Speichererkrankung Mukopolysaccharidose III Inaugural-Dissertation zur Erlangung der Doktorwürde der Hohen Medizinischen Fakultät der Universität zu Köln vorgelegt von Victor Mauri aus Stuttgart promoviert am 29. Januar 2014 Gedruckt mit Genehmigung der Medizinischen Fakultät der Universität zu Köln, 2014 Dekan: Universitätsprofessor Dr. med. Dr. h.c. Th. Krieg 1. Berichterstatterin: Frau Universitätsprofessor Dr. rer. nat. B. Wirth 2. Berichterstatter: Professor Dr. rer. nat. F.-G. Hanisch Erklärung Ich erkläre hiermit, dass ich die vorliegende Dissertationsschrift ohne unzulässige Hilfe Dritter und ohne Benutzung anderer als der angegebenen Hilfsmittel angefertigt habe; die aus fremden Quellen direkt oder indirekt übernommenen Gedanken sind als solche kenntlich gemacht. Bei der Auswahl und Auswertung des Materials sowie bei der Herstellung des Manuskriptes habe ich Unterstützungsleistungen von folgenden Personen erhalten: Univ.-Prof. Dr. rer. nat. Brunhilde Wirth Marco Sardiello, PhD, Assistant Professor BCM Christian Schaaf, MD, PhD, Assistant Professor BCM Weitere Personen waren an der geistigen Herstellung der vorliegenden Arbeit nicht beteiligt. Insbesondere habe ich nicht die Hilfe einer Promotionsberaterin/eines
    [Show full text]
  • Allosteric Activation of Yeast Enzyme Neutral Trehalase by Calcium and 14-3-3 Protein
    Physiol. Res. 68: 147-160, 2019 https://doi.org/10.33549/physiolres.933950 REVIEW Allosteric Activation of Yeast Enzyme Neutral Trehalase by Calcium and 14-3-3 Protein M. ALBLOVA1, A. SMIDOVA1, D. KALABOVA1, D. LENTINI SANTO2, T. OBSIL1,2, V. OBSILOVA1 1Department of Structural Biology of Signaling Proteins, Division BIOCEV, Institute of Physiology of the Czech Academy of Sciences, Vestec, Czech Republic, 2Department of Physical and Macromolecular Chemistry, Faculty of Science, Charles University, Prague, Czech Republic Received May 30, 2018 Accepted October 3, 2018 Epub Ahead of Print January 10, 2019 Summary ergot of rye in 1832. Trehalose has been known as Neutral trehalase 1 (Nth1) from Saccharomyces cerevisiae trehalose since 1858 when Marcellin Berthelot isolated catalyzes disaccharide trehalose hydrolysis and helps yeast to this disaccharide as sweet trehala manna from weevil survive adverse conditions, such as heat shock, starvation or cocoons (reviewed in Elbein 1974, Nwaka and Holzer oxidative stress. 14-3-3 proteins, master regulators of hundreds 1998). In the following decades, trehalose was discovered of partner proteins, participate in many key cellular processes. also in the yeast S. cerevisiae (Koch and Koch 1925) and Nth1 is activated by phosphorylation followed by 14-3-3 protein in bacteria, plants, fungi, insects and other invertebrates (Bmh) binding. The activation mechanism is also potentiated by but never in mammals (Elbein 1974, Thevelein 1984b, Ca2+ binding within the EF-hand-like motif. This review Nwaka and Holzer 1998). Because no trehalose synthesis summarizes the current knowledge about trehalases and the molecular and structural basis of Nth1 activation. The crystal has been shown in vertebrates, the trehalose pathway can structure of fully active Nth1 bound to 14-3-3 protein provided be a target for the development of drugs against the first high-resolution view of a trehalase from a eukaryotic pathological fungi (Van Dijck et al.
    [Show full text]
  • Agency Response Letter GRAS Notice No. GRN 000727
    Vincent Sewalt, Ph.D. Senior Director, Product Stewardship & Regulatory Danisco US Inc. (Operating as DuPont Industrial Biosciences) 925 Page Mill Road Palo Alto, CA 94304 Re: GRAS Notice No. GRN 000727 Dear Dr. Sewalt: The Food and Drug Administration (FDA, we) completed our evaluation of GRN 000727. We received Danisco US Inc., operating as DuPont Industrial Biosciences’ (DuPont), notice on August 18, 2017, and filed it on October 19, 2017. We received an amendment that addressed our questions regarding the molecular weight of trehalase on December 12, 2017. The subject of the notice is trehalase enzyme preparation produced by Trichoderma reesei expressing a trehalase gene from T. reesei (trehalase enzyme preparation) for use as an enzyme in the manufacture of organic acids (e.g., lactic, citric, and succinic acid), monosodium glutamate, and potable alcohol, at levels up to 36.7 mg Total Organic Solids (TOS) trehalase enzyme preparation/kg starch. The notice informs us of DuPont’s view that these uses of trehalase enzyme preparation are GRAS through scientific procedures. Commercial enzyme preparations that are used in food processing typically contain an enzyme component that catalyzes the chemical reaction as well as substances used as stabilizers, preservatives, or diluents. Enzyme preparations may also contain components derived from the production organism and components derived from the manufacturing process, e.g., constituents of the fermentation media or the residues of processing aids. DuPont’s notice provides information about each of these components in the trehalase enzyme preparation. According to the classification system of enzymes established by the International Union of Biochemistry and Molecular Biology, trehalase is identified by the Enzyme Commission Number 3.2.1.28.
    [Show full text]
  • Characterization of a Trehalose-Degrading Enzyme from the Hyperthermophilic Archaeon Sulfolobus Acidocaldarius
    Journal of Bioscience and Bioengineering VOL. 122 No. 1, 47e51, 2016 www.elsevier.com/locate/jbiosc Characterization of a trehalose-degrading enzyme from the hyperthermophilic archaeon Sulfolobus acidocaldarius Jeong Hyun Moon, Whiso Lee, Jihee Park, Kyoung-Hwa Choi, and Jaeho Cha* Department of Microbiology, College of Natural Sciences, Pusan National University, 2, Busandaehak-ro 63beon-gil, Geumjeong-gu, Busan 46241, Republic of Korea Received 24 October 2015; accepted 15 December 2015 Available online 19 January 2016 We purified a cytosolic trehalase (TreH) from a thermoacidophilic archaeon Sulfolobus acidocaldarius. Enzyme activity in cell-free extracts indicated that trehalose degradation in the cell occurred via the hydrolytic activity of TreH, and not via TreP (phosphorolytic activity) or TreT (transfer activity). TreH was purified to near-homogeneity by DEAE anion- exchange chromatography, followed by size exclusion and HiTrap Q anion-exchange chromatography, and its molecu- lar mass was estimated as 40 kDa. Maximum activity was observed at 85C and pH 4.5. The half-life of TreH was 53 and 41 min at 90 C and 95 C, respectively. TreH was highly specific for trehalose and was inhibited by glucose with a Ki of 0.05 mM. Compared with TreH from other trehalases, TreH from S. acidocaldarius is the most thermostable trehalase reported so far. Furthermore, this is the first trehalase characterized in the Archaea domain. Ó 2015 The Society for Biotechnology, Japan. All rights reserved. [Key words: Trehalose; Trehalase; Sulfolobus acidocaldarius; Substrate specificity] In many microorganisms, cellular functions have evolutionarily above. TreX is a glycogen debranching enzyme that catalyzes the adapted to sudden changes in environments.
    [Show full text]
  • Purification and Characterization of Trehalase from Bacillus Sp. T3
    231 (Oyo Toshitsu Kagaku, Vo1..42, No.3, p.231-236 (1995)) Purification and Characterization of Trehalase from Bacillus sp. T3 Tetsuya NAKADA,* Shoji IKEGAMI,* Tomoyuki NIsHIMOTO, * Hiroto CHAEN,* Toshiyuki SUGIMOTO* and Masashi KURIMOTO* * Hayashibara Biochemical Laboratories , Inc. (7- 7, Amase- minamimachi, Okayama 700, Japan) A trehalase was highly purified from Bacillus sp. T3 newly isolated from soil at 50•BC . The molecular weight of the trehalase was estimated to be 58,000 Da by SDS-polyacrylamide gel electrophoresis and 52,000 Da by gel filtration. The pI of the enzyme was 4.8. Its optimum pH and temperature were around 7.8 and 50•BC, respectively. The enzyme was stable between pH 6.0-9.5, and below 55•BC . The Km value for trehalose was 3.0 mM. The enzyme was inactivated by Cu2+ and Hg2+. Trehalases (ƒ¿, ƒ¿-Trehalase; ƒ¿, ƒ¿-Trehalose prepared by the method reported by YAMAUCHI glucohydrolase [EC 3.2.1.28]) which hydrolyze and Aso.10) All other chemicals used were of trehalose to glucose are distributed in micro- the highest grade available. organisms, plants, insects and mammalian Microorganism. The microorganism, strain tissues.l) There are several reports of purifi- T3, used in this study was isolated from soil at cation and characterization of trehalases from 50t and was identified according to "Bergey's fungi,2,3) yeasts,4) bacteria,5) algae6) and insects.7) Manual of Systematic Bacteriology."11) Some enzymes have been considered to play an Cultivation. The bacterium was cultivated important role in spore germination or in aerobically in 30 l fermenter (B.
    [Show full text]
  • Studies on Theenzymology of Purified Preparations of Brush Border
    Biochem. J. (1973) 134, 43-57 43 Printed in Great Britain Studies on the Enzymology of Purified Preparations of Brush Border from Rabbit Kidney By S. G. GEORGE and A. J. KENNY Department of Biochemistry, University ofLeeds, 9 Hyde Terrace, Leeds LS2 9LS, U.K. (Received 16 November 1972) 1. A method for the preparation of brush border from rabbit kidneys is described. Contamination by other organelles was checked by electron microscopy and by the assay ofmarker enzymes and was low. 2. Seven enzymes, all hydrolases, were substantially enriched in the brush-border preparation and are considered to be primarily located in this structure. They are: alkaline phosphatase, maltase, trehalase, aminopeptidase A, aminopeptidase M, y-glutamyl transpeptidase and a neutral peptidase assayed by its ability to hydrolyse [1251]iodoinsulin B chain. 3. Adenosine triphosphatases were also present in the preparation, but showed lower enrichments. 4. Alkaline phosphatase was the most active phosphatase present in the preparation. The weak hydrolysis of AMP may well have been due to this enzyme rather than a specific 5'-nucleotidase. 5. The two disaccharidases in brush border were distinguished by the relative heat-stability of trehalase compared with that of maltase. 6. The individuality of the four peptidases was established by several means. The neutral peptidase and aminopeptidase M, both of which can attack insulin B chain, differed not only in response to inhibitors and activators but also in the inhibitory effect of a guinea-pig antiserum raised to rabbit aminopeptidase M. This antiserum inhibited both the purified and the brush-border activities of amino- peptidase M.
    [Show full text]
  • Chitin Biosynthesis Inhibition of Meloidogyne Incognita by Rnai-Mediated Gene Silencing Increases Resistance to Transgenic Tobacco Plants
    International Journal of Molecular Sciences Article Chitin Biosynthesis Inhibition of Meloidogyne incognita by RNAi-Mediated Gene Silencing Increases Resistance to Transgenic Tobacco Plants 1, 1, 1 1 Vimalraj Mani y, Chinreddy Subramanyam Reddy y , Seon-Kyeong Lee , Soyoung Park , Hyoung-Rai Ko 2, Dong-Gwan Kim 3 and Bum-Soo Hahn 4,* 1 Department of Agricultural Biotechnology, National Institute of Agricultural Sciences, Rural Development Administration, Jeonju 54874, Korea; [email protected] (V.M.); [email protected] (C.S.R.); [email protected] (S.-K.L.); [email protected] (S.P.) 2 Crop Protection Division, National Institute of Agricultural Sciences, Rural Development Administration, Wanju 55365, Korea; [email protected] 3 Department of Bio-Industry and Bio-Resource Engineering, Sejong University, Seoul 05006, Korea; [email protected] 4 National Agrobiodiversity Center, National Institute of Agricultural Sciences, Rural Development Administration, Jeonju 54874, Korea * Correspondence: [email protected]; Tel.: +82-63-238-4930 These Authors contributed equally. y Received: 23 July 2020; Accepted: 8 September 2020; Published: 10 September 2020 Abstract: Meloidogyne incognita is a devastating plant parasitic nematode that causes root knot disease in a wide range of plants. In the present study, we investigated host-induced RNA interference (RNAi) gene silencing of chitin biosynthesis pathway genes (chitin synthase, glucose-6-phosphate isomerase, and trehalase) in transgenic tobacco plants. To develop an RNAi vector, ubiquitin (UBQ1) promoter was directly cloned, and to generate an RNAi construct, expression of three genes was suppressed using the GATEWAY system. Further, transgenic Nicotiana benthamiana lines expressing dsRNA for chitin synthase (CS), glucose-6-phosphate isomerase (GPI), and trehalase 1 (TH1) were generated.
    [Show full text]