p>The checksum is a form of redundancy check that is calculated from the sequence. It is useful for tracking sequence updates.,/p> ,p>It should be noted that while, in theory, two different sequences could have the same checksum value, the likelihood that this would happen is extremely low.,/p> ,p>However UniProtKB may contain entries with identical sequences in case of multiple genes (paralogs).,/p> ,p>The checksum is computed as the sequence 64-bit Cyclic Redundancy Check value (CRC64) using the generator polynomial: x,sup>64,/sup> + x,sup>4,/sup> + x,sup>3,/sup> + x + 1. The algorithm is described in the ISO 3309 standard. ,/p> ,p class="publication">Press W.H., Flannery B.P., Teukolsky S.A. and Vetterling W.T.,br /> ,strong>Cyclic redundancy and other checksums,/strong>,br /> ,a href="http://www.nrbook.com/b/bookcpdf.php">Numerical recipes in C 2nd ed., pp896-902, Cambridge University Press (1993),/a>),/p> Checksum:i ...
BARROS, Márcio de; CELLIGOI, Maria Antonia P. Colabone; VIGNOLI, Josiane Alessandra and VARGAS, Lucia Helena Mendonça. Influence of ultrasound on sorbitol release by Zymomonas mobilis grown on high sucrose concentration. Braz. arch. biol. technol. [online]. 2006, vol.49, n.3, pp.371-374. ISSN 1678-4324. http://dx.doi.org/10.1590/S1516-89132006000400003.. This work investigated the effect of applying low intensity ultrasound on sorbitol release by Z.mobilis cultures grown on 200 g/L sucrose medium up to 48 h. The best sorbitol production was 36.09 g/L in 36 h culture. Ultrasound irradiation did not alter the sorbitol values detected after disrupting the cells with 20 minutes treatment.. Keywords : Zymomonas mobilis; sorbitol [ultrasound]. ...
Alkaline phosphatase with broad substrate specificity. Has phosphatase activity towards nucleotide and sugar phosphates with a preference to nucleotide phosphates. Has no phosphodiesterase activity.
Regulatory RNA regions within a transcript, particularly in the 5′ untranslated region (5′UTR), have been shown in a variety of organisms to control the expression levels of these mRNAs in response to various metabolites or environmental conditions. Considering the unique tolerance of Zymomonas mobilis to ethanol and the growing interest in engineering microbial strains with enhanced tolerance to industrial inhibitors, we searched natural cis-regulatory regions in this microorganism using transcriptomic data and bioinformatics analysis. Potential regulatory 5′UTRs were identified and filtered based on length, gene function, relative gene counts, and conservation in other organisms. An in vivo fluorescence-based screening system was developed to confirm the responsiveness of 36 5′UTR candidates to ethanol, acetate, and xylose stresses. UTR_ZMO0347 (5′UTR of gene ZMO0347 encoding the RNA binding protein Hfq) was found to down-regulate downstream gene expression under ethanol stress. Genomic
1H6B: Crystal Structures of the Precursor Form of Glucose-Fructose Oxidoreductase from Zymomonas Mobilis and its Complexes with Bound Ligands
Zymomonas mobilis subsp. mobilis (strain NCIB 11163) is a facultative aerobic, ethanol-producing bacterium. The natural habitat of this organism includes sugar-rich plant saps where the bacterium ferments sugar such as glucose or sucrose into ethanol and carbon dioxide. It is useful in industrial production systems, particularly in production of bioethanol for fuel. Genetically engineered strains that ferment pentoses in addition to naturally utilized hexoses also hold great promise for use in lignocellulosic biomass degradations. Z. mobilis is utilized for the conversion of sugars, particularly xylose, which is not utilized by another common sugar-fermenting organism such as yeast, to ethanol. Since xylose is a common breakdown product of cellulose or a waste component of the agricultural industry, it is an attractive source for ethanol production. Z. mobilis was chosen for this process as it is ethanol-tolerant (up to 120 grams of ethanol per litre) and productive (5-10% more ethanol than ...
(2005) Inui et al. Journal of Molecular Microbiology and Biotechnology. The central metabolic pathway of Corynebacterium glutamicum was engineered to produce ethanol. A recombinant strain which expressed the Zymomonas mobilis genes coding for pyruvate decarboxylase (pd...
The primary structure of the DNA-binding protein II from Zymomonas mobilis has been determined from data provided by automated… Expand ...
The enzyme tRNA-guanine transglycosylase (TGT, EC 2.4.2.29) catalyses a base-exchange reaction that leads to anticodon modifications of certain tRNAs. The TGT enzymes of the eubacteria Zymomonas mobilis (Z. mobilis TGT) and Escherichia coli (E. coli
Levansucrase gene ( levU) of Z. mobilis had been cloned and overexpressed in Escherichia coli (Song, K.-B. and Rhee, S.-K. (1994) Biotechnol. Lett.16, 1305-1310). The levansucrase was purified and...
1OFG: The structure of glucose-fructose oxidoreductase from Zymomonas mobilis: an osmoprotective periplasmic enzyme containing non-dissociable NADP.
1971, Swings Jean, UGent - Fac. Wetenschappen - Vakgroep Biochemie en Microbiologie, Labo voor Microbiologie <- 1969, W.Van Pee <- 1961, NCIB (Zymomonas mobilis) <- 1958, S.Elsden <- 1958, ATCC <- 1952, NRRL (Pseudomonas lindneri) <- 1948, Technische Universiteit Delft <- 1929, Lindner (Termobacterium mobile) (1925 ...
This study proposes simulations which present optimized methods for producing fatty acids, fatty alcohols and alkanes using Zymomonas mobilis bacterium by the energy efficient β-oxidation reversal pathway, an eco-friendly ...
Glucose-fructose syrup is commonly added to foods as a sweetener, in order not only to give a sweet taste, but also to increase the attractiveness of the product by improving consistency, aroma and color, but excessive consumption of products containing glucose-fructose syrup is a health risk. Why is glucose-fructose syrup harmful? Glucose-fructose syrup is a sweetener obtained in a technological process mainly from corn starch,… ...
Contrary to most other modified bases, queuine and archaeosine biosyntheses start outside the tRNA and require a base exchange at the tRNA level, a reaction catalyzed by enzymes known as tRNA-guanine transglycosylases (TGTs). Several groups have reported the isolation of the eukaryotic TGT, but these reports do not agree on its oligomeric state and the size of its subunits. An archaebacterial TGT has been isolated very recently. This enzyme is a 78-kDa protein that has been shown through partial sequencing to be sequence-related to the prokaryotic TGT. TGT is certainly one of the most interesting enzymes of the queuine biosynthesis pathway because it catalyzes a reaction (a base exchange) which is also observed in many other cellular processes involving DNA and RNA. The structure of Zymomonas mobilisTGT was solved by the well-known technique of multiple isomorphous replacement (MIR). The soaking approach employed with the small preQ1, molecule cannot be used with a tRNA macromolecule and the only way to
onsumer Medicine InformationWhat is in this leafletThis leaflet answers some common questions about Mobilis.It does not contain all the available information. It does not take the place of talking to your doctor or pharmacist.All medicines have benefits and risks. Your doctor has weighed the risks of you taking Mobilis against the benefits expected for you.If you have any concerns about taking this medicine, talk to your doctor or pharmacist.Keep this leaflet with your medicine. You may need to read..
Fructose-Glucose Syrup as sugar replacement and sweetener: Information, tolerance and effect of Fructose-Glucose Syrup within the human body - Frusano
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glucose-fructose-syrup definition: Noun (plural glucose-fructose syrups) 1. (UK) high fructose corn syrupI dont drink anything let alone eat anything with glucose-fructose syrup in it, its not natural.Origin glucose-fructose + syrup...
CP4 (UFPEDA-202) was studied in a Wistar rat model fed the 109 colony forming units (cfu)/mL-1 of the assayed strain for 30 days. No abnormal clinical signs were noted in the group receiving viable cells of Z. mobilis and water (control) during the period of the experiment. There were no significant difference (p > 0.05) in feed intake and weight gain among mice fed the Z. mobilis in comparison to the control group. No bacteria were found in blood, liver and spleen of any animals. Mice receiving Z. mobilis showed significantly differences (p < 0.05) in total and differential leucocytes count, excepting for neutrophils, after the experimental period. Otherwise, it was not found in control group. Histological examination showed that feeding mice with Z. mobilis caused no signs of adverse effects on gut, liver and spleen. From these results, Z. mobilis CP4 (UFEPEDA-202) is likely to be nonpathogenic and safe for consumption, and could have a slight modulating effect on immunological performance in ...
Hi everyone! I am looking for a rapid method to screen glycerol-producing microorganisms. There are about 12000 candidates I have to screen. There is a paper in Journal of Microbiological Methods (1983) 339-342: A rapid screening method to detect ethanol production by microorganisms by Cornelius Johannes Jacobs, Bernard Alexander Prior, and Micahel Josias de Kock. They used enzyme and certain dyes then poured them directly on the petri plate, the ethanol-producing organims will have a certain distinctive color. I would really appreciate it if you could inform me where I can find a similar method for glycerol, or any other methods you think is applicable. Please e-mail me, any suggestions welcomed. Thank you. Charles Kosan kosanc at caelab1.cae.wisc.edu ...
Investigation of Specificity Determinants in Bacterial tRNA-Guanine Transglycosylase Reveals Queuine, the Substrate of Its Eucaryotic Counterpart, as Inhibitor. . Biblioteca virtual para leer y descargar libros, documentos, trabajos y tesis universitarias en PDF. Material universiario, documentación y tareas realizadas por universitarios en nuestra biblioteca. Para descargar gratis y para leer online.
In this thesis multiple computer aided methods of structure based drug design along with X-ray crystallography and kinetic measurements were used to investigate inhibitors of tRNA-guanine transglycosylase (TGT) a putative target for a new specific antibiotic against Shigella bacteria. Within a year about 160 million infections are reported leading to approximately 1 million deaths, predominantly in developing. The crystallization of Z. mobilis TGT, which offers a nearly identical active site as TGT from S. flexneri, was successfully performed in previous studies. Several scaffolds based on pyridazinones, pteridines, and quinazolinones were discovered with binding affinities in the micro molar range. In addition, a "stretched" guanine with an inserted central six-membered ring, leading to lin-benzoguanine (3 µM), was discovered and further evaluated in this thesis. During the optimization process of the lin-benzoguanine skeleton two often neglected aspects of ligand binding to a protein are ...
Future corn availability: Forecasts show an anticipated increase in corn yields over the next 10 years of 17 percent, resulting in an estimated increase in Nebraska corn production from 1.27 billion bushels for the 2005-06 crop year to 1.51 billion bushels for the 2015-16 crop year. Projections of feed use for the same period show a significant decrease due to the additional availability of the distillers grains products ...
In molecular biology, glycoside hydrolase family 68 is a family of glycoside hydrolases. Glycoside hydrolases EC 3.2.1. are a widespread group of enzymes that hydrolyse the glycosidic bond between two or more carbohydrates, or between a carbohydrate and a non-carbohydrate moiety. A classification system for glycoside hydrolases, based on sequence similarity, has led to the definition of >100 different families. This classification is available on the CAZy(http://www.cazy.org/GH1.html) web site, and also discussed at CAZypedia, an online encyclopedia of carbohydrate active enzymes. The glycosyl hydrolase 68 family (CAZY GH_68) includes several bacterial levansucrase enzymes, and invertase from Zymomonas. Levansucrase (EC 2.4.1.10), also known as beta-D-fructofuranosyl transferase, catalyses the conversion of sucrose and (2,6-beta-D-fructosyl)(N) to glucose and (2,6-beta-D-fructosyl)(N+1), where other sugars can also act as fructosyl acceptors. Invertase, or extracellular sucrase (EC 3.2.1.26), ...
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the catalytic subunit of tRNA-guanine transglycosylase. tRNA-guanine transglycosylase is a heterodimeric enzyme complex that plays a critical role in tRNA modification by synthesizing the 7-deazaguanosine queuosine, which is found in tRNAs that code for asparagine, aspartic acid, histidine and tyrosine. A pseudogene of this gene is located on the long arm of chromosome X. [provided by RefSeq, Feb 2012 ...
The crystal structure of the complex of the thiamine diphosphate dependent tetrameric enzyme pyruvate decarboxylase (PDC) from brewers yeast strain with the activator pyruvamide has been determined to 2.4 A resolution. The asymmetric unit of the crystal contains two subunits, and the tetrameric molecule is generated by crystallographic symmetry. Structure analysis revealed conformational nonequivalence of the active sites. One of the two active sites in the asymmetric unit was found in an open conformation, with two active site loop regions (residues 104-113 and 290-304) disordered. In the other subunit, these loop regions are well-ordered and shield the active site from the bulk solution. In the closed enzyme subunit, one molecule of pyruvamide is bound in the active site channel, and is located in the vicinity of the thiazolium ring of the cofactor. A second pyruvamide binding site was found at the interface between the Pyr and the R domains of the subunit in the closed conformation, about 10 ...
The pdc1 gene encoding pyruvate decarboxylase has been isolated and sequenced from an IR54 rice genomic library. In contrast to a previously isolated intron-less rice genomic pdc, pRgpdc3, this gene contains five intervening introns in the coding region and corresponds to a cDNA clone, pRcpdc1, isolated from an IR54-cDNA library constructed from anaerobically-induced mRNAs. Comparison of the deduced amino acid sequence of this gene with that of the rice pdc2 and pdc3 showed 88% and 89% similarity, and 78% and 79% identity, respectively. Southern blots indicated that more than three genes constitute the pdc gene family in rice. pdc1 is highly inducible under anaerobic conditions. Rice pdc2 is also inducible by anoxia but to a much lesser extent than pdc1. ...
The Nova Scotia Business Journal. SCOTSBURN - It was very much like the pitch of a travelling salesman: the positive talking points came easy but the catch was hard to discern. About 100 farmers and their families showed up at Sandy Stewarts Scotsburn farm Thursday morning to listen to representatives of Atlantec Bioenergy Corporations plan to transform a part of this provinces agricultural landscape into an ethanol-producing hub.. It was the third tour presented by ABC and it drew in farmers from a 40 km radius, from Stewiacke to River John and back to Pictou. Ron Coles, the spokesperson for the company, says ABC doesnt pretend to be the solution to the agriculture crisis facing food-crop producers, but he will promise a long-term commitment from the company.. ABC has its eye on a part of the TrentonWorks facility and has put in a bid. Within the month, Coles said its likely theyll hear back from the receiver whether or not theyll be able to set up shop there. And ABC hopes farmers will ...
Pack of 600 Soft Foam Sweet Perfect For All Kids Parties Great Value Candy Ingredients: glucose-fructose syrup,sugar,water,pork gelatine,maize starch,flavou
Consolider les activités délevage menées dans le cadre du Programme national de désarmement, démobilisation et réinsertion (PN-DDR) pour la réinsertion socio-économique durable des ex-combattants démobilisés associés ...read more ...
Pyruvate decarboxylase (PDC) is a well-known pathway for ethanol production, but has not been demonstrated for high titer ethanol production at temperatures above 50 °C. Here we examined the thermostability of eight PDCs. The purified bacterial enzymes retained 20% of activity after incubation for 30 min at 55 °C. Expression of these PDC genes, except the one from Zymomonas mobilis, improved ethanol production by Clostridium thermocellum. Ethanol production was further improved by expression of the heterologous alcohol dehydrogenase gene adhA from Thermoanaerobacterium saccharolyticum. The best PDC enzyme was from Acetobactor pasteurianus. A strain of C. thermocellum expressing the pdc gene from A. pasteurianus and the adhA gene from T. saccharolyticum was able to produce 21.3 g/L ethanol from 60 g/L cellulose, which is 70% of the theoretical maximum yield.
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Interannual variability in precipitation, particularly drought, can affect lignocellulosic crop biomass yields and composition, and is expected to increase biofuel yield variability. However, the effect of precipitation on downstream fermentation processes has never been directly characterized. In order to investigate the impact of interannual climate variability on biofuel production, corn stover and switchgrass were collected during 3 years with significantly different precipitation profiles, representing a major drought year (2012) and 2 years with average precipitation for the entire season (2010 and 2013). All feedstocks were AFEX (ammonia fiber expansion)-pretreated, enzymatically hydrolyzed, and the hydrolysates separately fermented using xylose-utilizing strains of Saccharomyces cerevisiae and Zymomonas mobilis. A chemical genomics approach was also used to evaluate the growth of yeast mutants in the hydrolysates. While most corn stover and switchgrass hydrolysates were readily fermented, growth
ID A4AWT5_MARSH Unreviewed; 358 AA. AC A4AWT5; DT 03-APR-2007, integrated into UniProtKB/TrEMBL. DT 03-APR-2007, sequence version 1. DT 08-MAY-2019, entry version 88. DE RecName: Full=Queuine tRNA-ribosyltransferase {ECO:0000256,HAMAP-Rule:MF_00168, ECO:0000256,RuleBase:RU003777, ECO:0000256,SAAS:SAAS00087750}; DE EC=2.4.2.29 {ECO:0000256,HAMAP-Rule:MF_00168, ECO:0000256,RuleBase:RU003777, ECO:0000256,SAAS:SAAS00087822}; DE AltName: Full=Guanine insertion enzyme {ECO:0000256,HAMAP-Rule:MF_00168}; DE AltName: Full=tRNA-guanine transglycosylase {ECO:0000256,HAMAP-Rule:MF_00168}; GN Name=tgt {ECO:0000256,HAMAP-Rule:MF_00168}; GN OrderedLocusNames=FB2170_00065 {ECO:0000313,EMBL:EAQ99602.1}; OS Maribacter sp. (strain HTCC2170 / KCCM 42371). OC Bacteria; Bacteroidetes; Flavobacteriia; Flavobacteriales; OC Flavobacteriaceae; Maribacter. OX NCBI_TaxID=313603 {ECO:0000313,EMBL:EAQ99602.1, ECO:0000313,Proteomes:UP000001602}; RN [1] {ECO:0000313,EMBL:EAQ99602.1, ECO:0000313,Proteomes:UP000001602} RP ...
Cite as: IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic, J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8. https://doi.org/10.1351/goldbook. ...
The role of sugar in health has been long-contended. In part, this is because of all the differing definitions of sugar: raw, unrefined, cane, free, fructose, glucose, glucose-fructose, high fructose corn syrup... so why all the fuss? When you consume more sugar than your body needs, it stores the excess as fat - under the skin…
As far as I know, (as a Canadian cokaholic) only when they make special products that are Kosher for Passover. Because eating corn or corn products is forbidden to Jews during passover. Thats when I seek out a Jewish neighborhoud and stock up on the good stuff. It DOES taste better. The flavour is smoother, more subtle. You could do the same in the USA. I believe the labeling in the USA is stricter and "corn syrup" is listed - in Canada they can say "glucose-fructose" without giving the source. ...
As far as I know, (as a Canadian cokaholic) only when they make special products that are Kosher for Passover. Because eating corn or corn products is forbidden to Jews during passover. Thats when I seek out a Jewish neighborhoud and stock up on the good stuff. It DOES taste better. The flavour is smoother, more subtle. You could do the same in the USA. I believe the labeling in the USA is stricter and "corn syrup" is listed - in Canada they can say "glucose-fructose" without giving the source. ...
TABLE-US-00002 Program: CLUSTALW, Default parameters: Protein Gap Open Penalty 10.0 Protein Gap Extension Penalty 0.2 Protein weight matrix: Gonnet series GI No. of the reference S_ID DB SEQ ID NO Organism sequences Aa Position s1 seq_ID 2 Zymomonas mobilis AAV90172.1 F 486 s20 seq_ID 3 Streptomyces coelicolor CAB39697.1 F 449 s911 seq_ID 4 Acetobacter pasteurianus BAH99456.1 F 481 s2 seq_ID 5 Bradyrhizobium sp. ABQ33590.1 F 447 s940 seq_ID 6 Zymomonas mobilis EER62728.1 F 438 s949 seq_ID 7 Acidithiobacillus caldus EET25937.1 Y 432 s167 seq_ID 8 Acidithiobacillus ferrooxidans ACH84004.1 Y 429 s41 seq_ID 9 Acidobacterium capsulatum ACO34244.1 F 458 s36 seq_ID 10 Acidothermus cellulolyticus ABK53469.1 F 426 s83 seq_ID 11 Adiantum capillus-veneris BAF93209.1 Y 436 s143 seq_ID 12 Ajellomyces capsulatus EDN09769.1 F 496 s995 seq_ID 13 Ajellomyces capsulatus EER40510.1 -- 432 s163 seq_ID 14 Ajellomyces capsulatus EEH02950.1 F 429 s13 seq_ID 15 Alicyclobacillus acidocaldarius EED08231.1 Y 420 s14 ...
In the late 1980s R. planticola was genetically modified by inserting a plasmid from Zymomonas mobilis. This plasmid codes for the enzyme pyruvate decarboxylase which, along with alcohol dehydrogenase already present in the bacteria allow it to produce ethanol. The bacteria already does produce ethanol when metabolizing hexoses and pentoses, but very inefficiently. R. planticola was chosen to receive this gene as it already had metabolic pathways to breakdown pentose sugars such as xylose, which is a main component of agricultural and forest residues.[22][23] The results showed that the genetically modified strain could produce ethanol but were killed at concentrations of ethanol greater than 5%. The modified strain also produced more ethanol at lower pH (5.4) and ethanol production decreased as pH increased.[22]. In the early 1990s a biotech company set out to solve a problem: how to destroy crop residue safely. Some crops residues harbor plant pathogens. Burning is occasionally used to ...
Citation: N/A Interpretive Summary: Technical Abstract: Biomass from agricultural residues is a potential low-cost feedstock for commercial ethanol production. Recombinant Escherichia coli that express the pet (production of ethanol) genes convert the glucose, xylose, and arabinose derived from lignocellulose to ethanol. To improve the stability of ethanol fermentations, we developed a series of ethanol-producing E. coli strains by transforming the pet operon into strains that cannot grow anaerobically. Due to mutations in the lactate dehydrogenase and pyruvate formate lyase genes, the cells are unable to reduce pyruvate and reoxidize the NADH generated in glycolysis. In our E. coli FBR strains, the pet genes (pyruvate decarboxylase and alcohol dehydrogenase encoded on pLOI297) complement the mutations and allow anaerobic growth by providing an alternate pathway for oxidation of NADH. In this scheme, the pet plasmid is exceptionally stable, without the addition of antibiotics. We have applied ...
302735543 - EP 0576621 B1 2001-02-28 - ETHANOL PRODUCTION BY RECOMBINANT HOSTS - [origin: WO9216615A1] Novel plasmids comprising genes which code for the alcohol dehydrogenase and pyruvate decarboxylase are described. Also described are recombinant hosts which have been transformed with genes coding for alcohol dehydrogenase and pyruvate. By virtue of their transformation with these genes, the recombinant hosts are capable of producing significant amounts of ethanol as a fermentation product. Also disclosed are methods for increasing the growth of recombinant hosts and methods for reducing the accumulation of undesirable metabolic products in the growth medium of these hosts. Also disclosed are recombinant host capable of producing significant amounts of ethanol as a fermentation product of oligosaccharides and plasmids comprising genes encoding polysaccharases, in addition to the genes described above which code for the alcohol dehydrogenase and pyruvate decarboxylase. Further, methods are described
|p|Ingrédients : oranges 45%, sucre de canne, pain dépices 9% (sirop de glucose-fructose, farine de seigle (|strong|gluten)|/strong|, miel, poudre à lever : diphosphate disodique-carbonate, acide de sodium, caramel, huile de colza, s
U.S. ethanol production continued on a record pace in March. According to information from the Energy Information Administration (EIA), March 2010 ethanol production averaged more than 847,000 barrels per day (b/d). That is an increase of 207,000 b/d over March 2009 ...
The U.S. Energy Information Administration has revised its forecast for 2014 ethanol production in its February Short-Term Energy Outlook. The EIA now predicts the U.S. ethanol industry will produce an average of 908,000 barrels per day this year.
Caloris provides efficient ethanol evaporation systems-including custom and pre-packaged evaporators-for cost-efficient ethanol production. Read more.
The U.S. Energy Information Administration has published the February edition of its Short-Term Energy Outlook, maintaining its January forecast that ethanol production will average 1.03 million barrels per day in both 2018 and 2019.
Hungarian firm - Tisza-TK Projekt Kft - a major food and ingredients producer - is building a new plant that will process over half a million tonnes of maize per year by 2018.. The new plant will be built in Tiszapuspoki town, 134 km (83.26 miles) east of Budapest. With a capacity to produce an annual 230,000 tonnes of isosugar - a glucose-fructose syrup used in the food industry - as well as starch, alcohol and feed components, the new plant is expected to be built at a cost of 145 million euro ($161.39 million). Continue reading →. ...
2020) LreEF1A,, a translation elongation factor from Lilium regale, Is pivotal for cucumber mosaic virus and tobacco rattle virus infections and tolerance to salt and drought. International Journal of Molecular Sciences, 21 (6). Article 2083. Jia, Y., Selva, C., Zhang, Y., Li, B., McFawn, L.A., Broughton, S., Zhang, X., Westcott, S., Wang, P., Tan, C., Angessa, T., Xu, Y., Whitford, R. and Li, C. ...