Academic literature on the topic 'Sucrose Synthesis'

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Journal articles on the topic "Sucrose Synthesis"

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Bhuvaneswari, E., B. Sailaja, and S. Sivaprasad. "Impact of photoperiod on circadian sucrose and sucrase rhythms in the digestive system of silkworm, Bombyx mori." Journal of Applied and Natural Science 5, no. 1 (June 1, 2013): 230–41. http://dx.doi.org/10.31018/jans.v5i1.312.

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The impact of photoperiod on circadian sucrose and sucrase rhythms were analyzed in the digestive system of Bombyx mori under 12 hr light-dark cycle (LD), continuous light (LL) and continuous dark (DD). The rhythmic changes were interpreted as synthetic cycles in gut wall and release or uptake cycles in gut lumen. The gut wall comprised 6 sucrose synthetic cycles (SS cycles) under LD, LL and 5 under DD. The 24 hr rhythm of LD and LL was clock shifted to 28.8 hr under DD. In gut content, the sucrose rhythm showed 7 sucrose uptake cycles (SUcycles) under LD, 6 under LL and 5 under DD and the 24 hr rhythm of LD was clock shifted to 28.0 hr under LL and 34 hr under DD. In the gut wall sucrase rhythm maintained 7 SES cycles under LD and DD and 9 cycles under LL and its 24-hr rhythm is advanced to 18.2 hr. In the gut lumen 5 SER cycles under LD, 8 under LL and 6 under DD and its rhythm is advanced to 15 hr under LL and 20 hr under DD. Further analysis of data showed that LD favoured both synthesis and uptake of sucrose while LL, favoured the sucrase synthesis and its release.
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Dyer, Ulrich C., and Yoshito Kishi. "Synthesis of C-sucrose." Journal of Organic Chemistry 53, no. 14 (July 1988): 3383–84. http://dx.doi.org/10.1021/jo00249a056.

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Lunn, John Edward. "Evolution of Sucrose Synthesis." Plant Physiology 128, no. 4 (April 1, 2002): 1490–500. http://dx.doi.org/10.1104/pp.010898.

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Suzuki, Michio, and Christopher J. Pollock. "Extraction and characterization of the enzymes of fructan biosynthesis in timothy (Phleum pratense)." Canadian Journal of Botany 64, no. 9 (September 1, 1986): 1884–87. http://dx.doi.org/10.1139/b86-250.

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A preparation of phlein sucrase from seedling shoots of timothy (Phleum pratense L.) is described which catalyzed the synthesis of fructan with a mean molecular size of 34 000 using sucrose as the substrate. Activity was fully sedimentable at 25 000 × g, had a pH optimum of 7.0, and a Km for sucrose of 0.15 M. Activity was inhibited by β-mercaptoethanol and sodium diethyl dithiocarbamate. Raffinose and stachyose, but not members of the kestose series of oligofructans, could act as fructosyl donors in addition to sucrose. Formation of oligosaccharides during high molecular weight fructan synthesis was minimal, with synthesis occurring by a mechanism apparently analogous to bacterial levansucrase. These observations are discussed in relation to the in vivo patterns of fructan biosynthesis observed in different species of higher plants.
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Nakai, Tomonori, Naoto Tonouchi, Takayasu Tsuchida, Hitoshi Mori, Fukumi Sakai, and Takahisa Hayashi. "Synthesis of Asymmetrically Labeled Sucrose by a Recombinant Sucrose Synthase." Bioscience, Biotechnology, and Biochemistry 61, no. 11 (January 1997): 1955–56. http://dx.doi.org/10.1271/bbb.61.1955.

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Lay, Luigi, Francesco Nicotra, Cristina Pangrazio, Luigi Panza, and Giovanni Russo. "Synthesis of antimetabolites of sucrose." Journal of the Chemical Society, Perkin Transactions 1, no. 3 (1994): 333. http://dx.doi.org/10.1039/p19940000333.

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Song, Zi-juan, Shu-jun Li, Xi Chen, Li-mei Liu, and Zhan-qian Song. "Synthesis of insecticidal sucrose esters." Forestry Studies in China 8, no. 3 (September 2006): 26–29. http://dx.doi.org/10.1007/s11632-006-0019-2.

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Hisajima, S., Y. Arai, and T. A. Thorpe. "Sucrose synthesis in callus cultures." Biologia Plantarum 27, no. 1 (January 1985): 74–77. http://dx.doi.org/10.1007/bf02894639.

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Ehira, Shigeki, Satoshi Kimura, Shogo Miyazaki, and Masayuki Ohmori. "Sucrose Synthesis in the Nitrogen-Fixing Cyanobacterium Anabaena sp. Strain PCC 7120 Is Controlled by the Two-Component Response Regulator OrrA." Applied and Environmental Microbiology 80, no. 18 (July 7, 2014): 5672–79. http://dx.doi.org/10.1128/aem.01501-14.

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ABSTRACTThe filamentous, nitrogen-fixing cyanobacteriumAnabaenasp. strain PCC 7120 accumulates sucrose as a compatible solute against salt stress. Sucrose-phosphate synthase activity, which is responsible for the sucrose synthesis, is increased by salt stress, but the mechanism underlying the regulation of sucrose synthesis remains unknown. In the present study, a response regulator, OrrA, was shown to control sucrose synthesis. Expression ofspsA, which encodes a sucrose-phosphate synthase, andsusAandsusB, which encode sucrose synthases, was induced by salt stress. In theorrAdisruptant, salt induction of these genes was completely abolished. The cellular sucrose level of theorrAdisruptant was reduced to 40% of that in the wild type under salt stress conditions. Moreover, overexpression oforrAresulted in enhanced expression ofspsA,susA, andsusB, followed by accumulation of sucrose, without the addition of NaCl. We also found that SigB2, a group 2 sigma factor of RNA polymerase, regulated the early response to salt stress under the control of OrrA. It is concluded that OrrA controls sucrose synthesis in collaboration with SigB2.
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Szyszka, Łukasz, Piotr Cmoch, Aleksandra Butkiewicz, Mykhaylo A. Potopnyk, and Sławomir Jarosz. "Synthesis of Cyclotriveratrylene-Sucrose-Based Capsules." Organic Letters 21, no. 16 (August 7, 2019): 6523–28. http://dx.doi.org/10.1021/acs.orglett.9b02451.

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Dissertations / Theses on the topic "Sucrose Synthesis"

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Baik, Youngmin. "Carbothermal synthesis of aluminum nitride using sucrose." Thesis, McGill University, 1991. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=60643.

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In this work, the carbothermal reduction of Al$ sb2$O$ sb3$ to AlN was studied. Several kinds of aluminum oxides including $ alpha$-Al$ sb2$O$ sb3$, $ gamma$-Al$ sb2$O$ sb3$, $ theta$-Al$ sb2$O$ sb3$ and boehmite (AlOOH) were examined in order to observe the differences in reaction behaviour and powder characteristics obtained from each type of precursor. Cane sugar (sucrose) and carbon black were used as carbon sources. Reaction conditions studied were carbon to alumina ratio, temperature and reaction time. Sucrose resulted in a close-to-stoichiometric ratio of Al$ sb2$O$ sb3$:C (1:3.2) achieving full conversion to AlN and produced a regular powder morphology, whilst carbon black required higher ratio ($>$1:4) to reach full conversion with agglomeration of the AlN powder. The optimal reaction temperature was 1600$ sp circ$C with the reaction time being dependent on the Al$ sb2$O$ sb3$ source. The results of the thermodynamic study for the Al-N-O-C system suggest a solid-state reaction process which is consistent with the experimental observations. Moreover, flowing N$ sb2$ gas flushes out the product CO gas and thus forces the equilibrium in favour of AlN formation. Reaction mechanisms are proposed for the two forms of carbon precursor.
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Hawker, John Seth. "Sucrose and starch metabolism in leaves, storage organs and developing fruits of higher plants." Title page, contents and summary only, 1988. http://web4.library.adelaide.edu.au/theses/09SD/09sdh392.pdf.

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Lunn, John Edward. "The control of sucrose synthesis in non-photosynthetic tissues." Thesis, University of Cambridge, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.304460.

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Kochhar, Anuradha. "Assimilate partitioning and sucrose synthesis in Lamium album L." Thesis, University of Cambridge, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.624185.

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Verges, Alizee. "Computer-aided design and engineering of sucrose-utilizing transglucosylases for oligosaccharide synthesis." Thesis, Toulouse, INSA, 2015. http://www.theses.fr/2015ISAT0020/document.

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La synthèse d’oligosides complexes reste difficilement réalisable par voie chimique. Le recours aux catalyseurs enzymatiques permettrait de pallier aux contraintes de la chimie mais les enzymes naturelles ne présentent pas toujours les propriétés adéquates et nécessitent d’être optimisées par ingénierie moléculaire. Le couplage de la chimie et de biocatalyseurs conçus « sur mesure », peut offrir une alternative prometteuse pour explorer de nouvelles voies de synthèse des sucres, notamment pour la mise au point de glycovaccins. L’objectif de cette thèse a ainsi visé à mettre en œuvre des stratégies d’ingénierie semi-rationnelles de l’amylosaccharase de Neisseria polysaccharea (ASNp), une α-transglucosylase utilisant le saccharose comme substrat, afin de concevoir de nouvelles spécificités de substrats et d’étendre le potentiel de cette enzyme à catalyser de nouvelles réactions, permettant ainsi d’aller bien au-delà de ce que la Nature peut offrir. Dans une première étude, une approche assistée par ordinateur a été suivie afin de remodeler le site actif de l’enzyme (sous-sites +1, +2 et +3) pour la reconnaissance et la glucosylation en α-1,4 d’un accepteur disaccharidique non-naturel (l’allyl 2-deoxy-2-N-trichloroacetyl-β-D-glucopyranosyl-(1→2)-α-L-rhamnopyranose). Le produit attendu, un trisaccharide, est un précurseur dans la synthèse chimio-enzymatique des oligosaccharides mimant les unités répétitives des lipopolysaccharides de Shigella flexneri, dont l’utilisation ultime est le développement de vaccins contre la Shigellose. Une approche computationnelle faisant appel à des outils dédiés au design automatisé de protéines et à une analyse des séquences a conduit au design d’une librairie d’environ 2.7x104 séquences, qui a ensuite été construite expérimentalement puis criblée. Au final, 55 variants actifs sur saccharose (le substrat donneur) ont été identifiés, et un mutant, appelé F3, a révélé sa capacité à glucosyler en α-1,4 le disaccharide cible. De manière étonnante, ce mutant possède 7 mutations au sein de son site actif, nécessaires au déploiement de sa nouvelle spécificité tout en maintenant son aptitude à utiliser le saccharose comme donneur d'unité glucosyle. Dans une deuxième étude, trois variants ont été identifiés lors du criblage de la librairie semi-rationnelle sur saccharose comme présentant de nouvelles spécificités de produits. Ces mutants ont été caractérisés plus en détails, ainsi que leurs produits, sur un plan biochimique et structural. Ces mutants, appelés 37G4, 39A8 et 47A10, contiennent entre 7 et 11 mutations dans leur site actif. Il a été montré qu’ils étaient capables de reconnaitre le saccharose et le maltose (un produit de la réaction avec le saccharose) comme donneur et accepteur pour synthétiser en quantités variables de l’erlose (α-D-Glucopyranosyl-(1→4)-α-D-Glucopyranosyl-(1→2)-β-D-Fructose) et du panose (α-D-Glucopyranosyl-(1→6)-α-D-Glucopyranosyl-(1→4)-α-D-glucose), des molécules non produites par l’enzyme sauvage. Des taux de production relativement élevés ont été obtenus pour ces molécules, dont les propriétés acariogènes et le pouvoir sucrant pourraient présenter un intérêt applicatif pour l’industrie alimentaire. Dans une dernière partie, un autre mutant, appelé 30H3, a été isolé lors du criblage primaire de la librairie de par son activité élevée sur saccharose (une amélioration d’un facteur 6.5 comparé à l’enzyme sauvage). Après caractérisation, le mutant s’est avéré synthétiser un profil unique de produits en comparaison de l’enzyme sauvage ASNp. Il s’est ainsi montré très efficace pour la synthèse de maltooligosaccharides solubles, de taille de chaînes contrôlée allant d’un DP 3 à 21, et de faible polydispersité. Aucun polymère insoluble n’a été identifié. La structure 3D du mutant résolue par cristallographie des rayons X a révélé un agrandissement de la poche catalytique en raison de la présence de 9 mutations introduites dans la première sphère
Chemical synthesis of complex oligosaccharides still remains critical. Enzymes have emerged as powerful tools to circumvent chemical boundaries of glycochemistry. However, natural enzymes do not necessarily display the required properties and need to be optimized by molecular engineering. Combined use of chemistry and tailored biocatalysts may thus be attractive for exploring novel synthetic routes, especially for glyco-based vaccines development. The objective of this thesis was thus to apply semi-rational engineering strategies to Neisseria polysaccharea amylosucrase (NpAS), a sucrose-utilizing α-transglucosylase, in order to conceive novel substrate specificities and extend the potential of this enzyme to catalyze novel reactions, going beyond what nature has to offer. In a first study, a computer aided-approach was followed to reshape the active site of the enzyme (subsites +1, +2 and +3) for the recognition and α-1,4 glucosylation of a non-natural disaccharide acceptor molecule (allyl 2-deoxy-2-N-trichloroacetyl-β-D-glucopyranosyl-(1→2)-α-L-rhamnopyranose). The trisaccharide product is a building block for the chemo-enzymatic synthesis of oligosaccharides mimicking the repetitive units of the Shigella flexneri lipopolysaccharides, and ultimately, for the production of a vaccine against Shigellosis disease. Using computational tools dedicated to the automated protein design, combined with sequence analysis, a library of about 2.7x104 sequences was designed and experimentally constructed and screened. Altogether, 55 mutants were identified to be active on sucrose (the donor substrate), and one, called mutant F3, was subsequently found able to catalyze the α-1,4 glucosylation of the target disaccharide. Impressively, this mutant contained seven mutations in the first shell of the active site leading to a drastic reshaping of the catalytic pocket without significantly perturbing the original specificity for sucrose donor substrate. In a second study, three variants were identified from the screening of the semi-rational library on sole sucrose as displaying totally novel product specificities. They were further characterized, as well as their products, at both biochemical and structural level. These mutants, called 37G4, 39A8 and 47A10, contained between 7 and 11 mutations into their active site. They were found able to use sucrose and maltose (a reaction product from sucrose) as both donor and acceptor substrates to produce in varying amounts erlose (α-D-Glucopyranosyl-(1→4)-α-D-Glucopyranosyl-(1→2)-β-D-Fructose) and panose (α-D-Glucopyranosyl-(1→6)-α-D-Glucopyranosyl-(1→4)-α-D-glucose) trisaccharides, which are not produced at all by parental wild-type enzyme. Relatively high yields were obtained for the production of these molecules, which are known to have acariogenic and sweetening properties and could be of interest for food applications. In a last part, another mutant 30H3 was isolated due to its high activity on sucrose (6.5-fold improvement compared to wild-type activity) from primary screening of the library. When characterized, the mutant revealed a singular product profile compared to that of wild-type NpAS. It appeared highly efficient for the synthesis of soluble maltooligosaccharides of controlled size chains, from DP 3 to 21, and with a low polydispersity. No formation of insoluble polymer was found. The X-ray structure of the mutant was determined and revealed the opening of the catalytic pocket due to the presence of 9 mutations in the first sphere. Molecular dynamics simulations suggested a role of mutations onto flexibility of domain B’ that might interfere with oligosaccharide binding and explain product specificity of the mutant
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Baguma, Yona. "Regulation of starch synthesis in cassava /." Uppsala : Dept. of Plant Biology and Forest Genetics, Swedish Univ. of Agricultural Sciences, 2004. http://epsilon.slu.se/a478.pdf.

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Konishi, Teruko. "THE EXPRESSION OF SUCROSE SYNTHASE AND ITS ROLE IN PLANT β-GLUCAN SYNTHESIS." Kyoto University, 2002. http://hdl.handle.net/2433/149898.

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Kyoto University (京都大学)
0048
新制・課程博士
博士(農学)
甲第9606号
農博第1234号
新制||農||841(附属図書館)
学位論文||H14||N3638(農学部図書室)
UT51-2002-G364
京都大学大学院農学研究科応用生命科学専攻
(主査)教授 酒井 富久美, 教授 關谷 次郎, 教授 島田 幹夫
学位規則第4条第1項該当
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Gerber, Jacqués. "The phloem unloading and sucrose-sequestration pathway in the internodal stem tissue of the Saccharum hybrid var. NCo376." Thesis, Rhodes University, 2001. http://hdl.handle.net/10962/d1003763.

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Internodes 5-8, 10, 13 and 15 of Saccharum sp. var. NCo376 were examined for evidence of symplasmic phloem unloading of sucrose from the phloem, via the bundle sheath to the storage parenchyma. The vascular bundle possesses wellisolated phloem comprised of large diameter sieve elements and small diameter companion cells. A layer of phloem parenchyma surrounds the phloem, except where the phloem abuts the crushed protophloem. Outside this is a sclerenchymatous sheath, directly endarch to a parenchymatous bundle sheath, which is surrounded by storage parenchyma. The bundle sheath is interrupted at the centrifugal pole of the vascular bundle by a phloem fibre cap. Scanning Electron Microscopy revealed plasmodesmal fields throughout the bundle sheath and pith tissue. Transmission Electron Microscopy studies provided evidence of plasmodesmal occlusion, but not in all tissues. Aniline blue reactions under UV light indicate the presence of occluded plasmodesmal fields at the phloem parenchyma / sclerenchymatous sheath interface, and in localised regions of cells which are smaller than the surrounding storage parenchyma cells. This suggests a symplasmic transport pathway at these locations, and, based on these positive aniline blue reactions, with regulation via callose-mediated transplasmodesmal transport. Osmotic stress experiments, which included the addition of Ca2+, did not reveal further callose occlusion in the parenchyma, suggesting that the plasmodesmata in these regions may be closed via a noncallosic mechanism. Dye-coupling studies, using Lucifer Yellow (LYCH), which was iontophoretically injected following turgor-pressure equalisation, showed only rare, limited symplastic transport, usually only between the injected cell and one adjacent cell. Most injections did not result in transport of LYCH, suggesting either a lack of plasmodesmal connectivity, occlusion, or gating of any plasmodesmata present. This limited symplasmic transport, combined with the presence of occluded plasmodesmata at the phloem parenchyma / sclerenchymatous sheath interface suggests the presence of a two-domain phloem-unloading pathway. While symplastic transport may occur from the phloem to the sclerenchymatous sheath, further sucrose transport to the storage parenchyma appears to proceed apoplasmically from the sclerenchymatous sheath / bundle sheath interface, and into storage parenchyma cells across the cell wall and cell membrane via specialised sucrose transporters.
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Nell, Hanlie. "Genetic manipulation of sucrose-storing tissue to produce alternative products." Thesis, Link to the online version, 2007. http://hdl.handle.net/10019/1136.

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Trollope, Kim Mary. "Engineering a fungal β-fructofuranosidase." Thesis, Stellenbosch : Stellenbosch University, 2015. http://hdl.handle.net/10019.1/96757.

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Thesis (PhD)--Stellenbosch University, 2015.
ENGLISH ABSTRACT: β-fructofuranosidases are hydrolytic enzymes that act on sucrose to yield the products glucose and fructose. Under high substrate conditions these enzymes display fructosyltransferase activity which results in the synthesis of fructooligosaccharides (FOS). Some enzymes display higher propensities for FOS synthesis than others, with the determinants of this activity remaining unclear. The consumption of FOS produces a prebiotic effect that positively alters the composition of the colonic microflora, and as a result is linked to improved human and animal health. The increased demand for FOS has necessitated the industrial production of these nutraceuticals. In enzymatic sucrose biotransformation processes operating at high substrate loading and temperatures between 50 and 60°C, β-fructofuranosidase activity is negatively influenced by glucose product inhibition and thermal instability. The aim of this study was therefore to engineer the Aspergillus japonicus β-fructofuranosidase, FopA, to improve a FOS synthesis bioprocess. A dual approach was employed to engineer FopA so as to increase the probability of obtaining an improved enzyme variant(s). A random mutagenesis approach was applied to harness the potential of the randomness of introduced mutations as precise structural knowledge of the enzyme regions involved in the phenotypic presentation of product inhibition, specific activity and thermal stability was unavailable. A semi-rational approach afforded the additional opportunity to reduce the number of variants to be screened, yet theoretically increased the functional content of the library. This study details the development of a method to rapidly quantify FOS using Fourier transform mid infrared attenuated total reflectance spectroscopy and multivariate data analysis. The method offers improvements over conventionally used high performance liquid chromatography in terms of reduced sample analysis times and the absence of toxic waste products. This is the first report on the direct screening of an enzyme variant library for FOS synthesis to identify improved variants and will significantly support future engineering of β-fructofuranosidases using random mutagenesis approaches. The random mutagenesis approach yielded a variant displaying limited relief from glucose inhibition. At the peak difference in performance, the variant produced 28% more FOS from the same amount of sucrose, when compared to the parent. The semi-rational approach, using a combined crystal structure and evolutionary-guided approach, yielded a four amino acid combination variant displaying improved specific activity and thermostability that was able to reduce the time to completion of an industrial-like FOS synthesis reaction by 26%. The positive outcome of the semi-rational approach showed that engineering loops regions in an enzyme is a feasible strategy to improve both specific activity and thermostability, most probably due to the modification of enzyme structural flexibility. A bioinformatic tool that enables the identification of β-fructofuranosidases displaying high-level FOS synthesis from protein sequence alone was also developed during the study. These investigations revealed conserved sequence motifs characteristic of enzymes displaying low- and high-level FOS synthesis and a structural loop, unique to the latter group, that were readily applicable identifiers of FOS synthesis capacity. The tool presented may also be useful to improve the understanding of the structure-function relationships of β-fructofuranosidases by facilitating the identification of variations in groups of enzymes that have been functionally sub-classified.
AFRIKAANSE OPSOMMING: β-fruktofuranosidases is hidrolitiese ensieme wat op sukrose inwerk en glukose en fruktose as produkte vorm. Onder toestande met hoë substraatkondisies vertoon hierdie ensieme fruktosieltransferase-aktiwiteit wat tot die sintese van frukto-oligosakkariede (FOS) lei. Sommige ensieme neig na ʼn hoër FOS-sintese as ander, maar die bepalende faktore vir hierdie aktiwiteit is nog onbekend. Die verbruik van FOS veroorsaak ʼn prebiotiese effek wat die samestelling van kolon mikroflora positief beïnvloed en met verhoogde mens- en dieregesondheid verbind word. Die verhoogde aanvraag vir FOS het die industriële produksie van hierdie nutraseutiese middel genoodsaak. Tydens ensiemgedrewe sukrose-biotransformasieprosesse by hoë substraatladings en temperature tussen 50 en 60 °C, word β-fruktofuranosidase-aktiwiteit negatief deur glukose produkonderdrukking en termiese onstabiliteit beïnvloed. Die doel van hierdie studie was dus om die Aspergillus japonicus β-fruktofuranosidase, FopA, vir ʼn verbeterde FOS-sintese bioproses te manipuleer. ʼn Tweeledige benadering is vir FopA manipulasie gevolg om die waarskynlikheid van verbeterde variant(e) te verhoog. ʼn Lukrake mutagenese benadering, wat die potensiaal van ingevoegde mutasie ewekansigheid inspan, is in die lig van onvoldoende akkurate kennis van die strukturele gedeeltes betrokke by produkinhibisie-, spesifieke aktiwiteit- en termiese stabiliteit fenotipes gevolg. Die toepassing van ʼn semi-rasionele benadering het ook geleentheid vir die sifting van ʼn kleiner variantbibioloteek geskep, terwyl die funksionele inhoud teoreties verhoog word. Die studie beskryf die ontwikkeling van ʼn metode vir die vinnige kwantifisering van FOS, gebaseer op Fourier transform middel infrarooi geattenueerde totale refleksie spektroskopie en meerveranderlike data-analise. Dit is die eerste melding van ʼn direkte sifting van ʼn ensiemvariantversameling vir FOS-sintese om verbeterde variante te identifiseer, en kan die toekomstige manipulasie van β-fruktofuranosidases deur middel van lukrake mutagenese-benaderings beduidend ondersteun. Die lukrake mutagenese-benadering het ʼn variant met beperkte opheffing van glukose-onderdrukking gelewer. By die punt waar die prestasie die meeste verskil, het die variant 28% meer FOS vanaf dieselfde hoeveelheid sukrose geproduseer in vergelyking met die ouer-ensiem. Die semi-rasionele benadering, gegrond op ʼn kombinasie van kristalstruktuur en evolusionêre-geleide benaderings, het ʼn vier-aminosuurkombinasie variant met hoër spesifieke aktiwiteit en termostabiliteit gelewer wat die voltooiingstyd van ʼn tipiese industriële FOS sintesereaksie met 26% kon verkort. Die positiewe uitkoms van die semi-rasionele benadering het aangedui dat manipulasie van die lusgedeeltes in ʼn ensiem ʼn lewensvatbare strategie is om beide spesifieke aktiwiteit en termostabiliteit te verbeter, moontlik as gevolg van wysigings in die buigsaamheid van die ensiemstruktuur. ʼn Bioïnformatika-hulpmiddel vir die identifikasie van β-fruktofuranosidases met hoë vlakke van FOS-sintese op grond van proteïenvolgordes is ook tydens die studie ontwikkel. Motiewe met gekonserveerde volgordes kenmerkend van lae- en hoë-vlak FOS-produserende ensieme en ʼn strukturele lus, uniek tot die laasgenoemde groep, is tydens die ondersoek onthul wat as maklike identifiseerders van FOS-sintesekapasiteit kan dien. Die voorgestelde hulpmiddel kan ook nuttig wees om die struktuur-funksie-verwantskap van β-fruktofuranosidases beter te verstaan deur die identifikasie van variasie in ensiemgroepe wat funksioneel gesubklassifiseer is.
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Books on the topic "Sucrose Synthesis"

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John, Philip. Biosynthesis of the major crop products: The biochemistry, cell physiology, and molecular biology involved in the synthesis by crop plants of sucrose, fructan, starch, cellulose, oil, rubber, and protein. Chichester: Wiley, 1992.

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Konowicz, Paul A. Some synthetic transformations on sucrose. Norwich: University of East Anglia, 1991.

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Book chapters on the topic "Sucrose Synthesis"

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Stitt, Mark. "Limitation of Photosynthesis by Sucrose Synthesis." In Progress in Photosynthesis Research, 685–92. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-017-0516-5_144.

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Sharkey, Thomas D., Marianne M. Laporte, Barry J. Micallef, Christine K. Shewmaker, and Jannette V. Oakes. "Sucrose Synthesis, Temperature, and Plant Yield." In Photosynthesis: from Light to Biosphere, 4527–32. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-009-0173-5_1063.

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Heldt, Hans W., and Mark Stitt. "The Regulation of Sucrose Synthesis in Leaves." In Progress in Photosynthesis Research, 675–84. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-017-0516-5_143.

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Jo, Seongbong, and Kinam Park. "Synthesis and Characterization of Thermoreversible Sucrose Hydrogels (Sucrogels)." In ACS Symposium Series, 113–26. Washington, DC: American Chemical Society, 1999. http://dx.doi.org/10.1021/bk-1999-0737.ch008.

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Stitt, Mark. "Application of Control Analysis to Photosynthetic Sucrose Synthesis." In Control of Metabolic Processes, 363–76. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4757-9856-2_32.

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HAYASHI, TAKAHISA, TERUKO KONISHI, YASUNORI OHMIYA, and TOMONORI NAKAI. "Is cellulose synthesis enhanced by expression of sucrose sysnthesis in poplar." In Abiotic stress tolerance in plants, 187–93. Dordrecht: Springer Netherlands, 2006. http://dx.doi.org/10.1007/1-4020-4389-9_13.

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Zervosen, Astrid, and Lothar Elling. "Application of Sucrose Synthase in the Synthesis of Nucleotide Sugars and Saccharides." In Carbohydrate Biotechnology Protocols, 235–54. Totowa, NJ: Humana Press, 1999. http://dx.doi.org/10.1007/978-1-59259-261-6_19.

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Paulino, C., and M. C. Arrabaça. "Synthesis of Sucrose and Fructans in Wheat Leaves: The Effects of Temperature." In Current Research in Photosynthesis, 3453–56. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0511-5_777.

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Suyama, Kyozo, and Susumu Adachi. "Enzymatic synthesis of new trisaccharide, isoraffinose, from a mixture of lactose and sucrose." In MILK the vital force, 223. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-3733-8_182.

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Yamada, Kouichi, and Jun Takezawa. "Measurement of DNA synthesis and strand breaks using alkaline sucrose density gradient centrifugation." In Subcellular Biochemistry, 435–38. Dordrecht: Springer Netherlands, 2006. http://dx.doi.org/10.1007/978-1-4020-4896-8_42.

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Conference papers on the topic "Sucrose Synthesis"

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Elling, Lothar, Ulrike Römer, and Walter Knöckenberger. "Characterization and Application of Recombinant Sucrose Synthase 1 from Potato for the Synthesis of Sucrose Analogues." In The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01930.

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Jin, Li, Fangtong Liu, and Jianpo Zhang. "THE SYNTHESIS AND CHARACTERIZATION OF SUCROSE MODIFIED MAGNETITE." In International Conference on New Materials and Intelligent Manufacturing (ICNMIM). Volkson Press, 2018. http://dx.doi.org/10.26480/icnmim.01.2018.164.166.

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Li, Quanhui, Jiaying Xin, Tingting Yao, Zhengyang Wang, and Luoyun Zheng. "The Microwave-assisted Lipase-catalyzed Synthesis of Sucrose Laurate." In International Conference on Electronics, Mechanics, Culture and Medicine. Paris, France: Atlantis Press, 2016. http://dx.doi.org/10.2991/emcm-15.2016.64.

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Maria, M. Ibadurrohman, and Slamet. "Synthesis of sucrose ester surfactant by utilizing molasses and waste cooking oil." In INTERNATIONAL CONFERENCE ON TRENDS IN MATERIAL SCIENCE AND INVENTIVE MATERIALS: ICTMIM 2020. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0013809.

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Naulidia, R. A., E. Juliana, S. Handayani, F. Damayanti, S. Setiasih, and S. Hudiyono. "Enzymatic synthesis of glycerol and sucrose-palm oil fatty acid esters produced and their potency as antimicrobial agents." In THE 8TH INTERNATIONAL CONFERENCE OF THE INDONESIAN CHEMICAL SOCIETY (ICICS) 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0001346.

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Titinchi, Salam J. J., Waheed Saban, Leslie Petrik, and Hanna S. Abbo. "Synthesis, Characterization and Physiochemical Properties of Platinum Supported on Mesoporous Carbon." In ASME 2011 9th International Conference on Fuel Cell Science, Engineering and Technology collocated with ASME 2011 5th International Conference on Energy Sustainability. ASMEDC, 2011. http://dx.doi.org/10.1115/fuelcell2011-54670.

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Ordered mesoporous carbon (OMC) has been prepared by impregnating the pores of the silica template (SBA-15) with liquid petroleum gas (LPG) or sucrose. The desired support (OMC) was obtained after dissolution with NaOH. Platinum nanoparticles were dispersed on ordered mesoporous carbons using Chemical Vapour Deposition (CVD) method and Pt(acac)2 as metal source. The resulting ordered mesoporous carbon possess a large surface area with high microporosity, and a controlled pore size distribution, High-quality carbon replicas of SBA-15 show an X-ray diffraction peak at low angle, which indicates that the structural periodicity of the (111) planes has been maintained. Their pore volume and specific surface area are high and the pore volume is almost entirely microporous. The synthesized Pt/OMC was characterized by powder X-Ray diffraction, HR-TEM, HR-SEM, EDS, thermogravimetric analysis, and nitrogen adsorption. The performance of Pt catalyst supported OMC was evaluated by electrochemical studies, which shows almost similar activity to the commercial catalyst.
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Bezler, N. V., and M. Yu Petyurenko. "Bacteria of Pseudomonas genus in sugar beet agrocenosis." In 2nd International Scientific Conference "Plants and Microbes: the Future of Biotechnology". PLAMIC2020 Organizing committee, 2020. http://dx.doi.org/10.28983/plamic2020.043.

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Bacteria of Pseudomonas genus able to fix nitrogen and to produce heteroauxin are developed on roots of sugar beet. Their isolation from rhizoplane and introduction onto surface of sugar beet leaf apparatus promotes development of aerobic spore-forming bacteria, ammonificators, and nitrogen immobilizators that activates growing of leaf blade growth, syntheses of sucrose and growth of beet roots.
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Cuppoletti, John. "Composite Synthetic Membranes Containing Native and Engineered Transport Proteins." In ASME 2008 Conference on Smart Materials, Adaptive Structures and Intelligent Systems. ASMEDC, 2008. http://dx.doi.org/10.1115/smasis2008-449.

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Our membrane transport protein laboratory has worked with material scientists, computational chemists and electrical and mechanical engineers to design bioactuators and sensing devices. The group has demonstrated that it is possible to produce materials composed native and engineered biological transport proteins in a variety of synthetic porous and solid materials. Biological transport proteins found in nature include pumps, which use energy to produce gradients of solutes, ion channels, which dissipate ion gradients, and a variety of carriers which can either transport substances down gradients or couple the uphill movement of substances to the dissipation of gradients. More than one type of protein can be reconstituted into the membranes to allow coupling of processes such as forming concentration gradients with ion pumps and dissipating them with an ion channel. Similarly, ion pumps can provide ion gradients to allow the co-transport of another substance. These systems are relevant to bioactuation. An example of a bioactuator that has recently been developed in the laboratory was based on a sucrose-proton exchanger coupled to a proton pump driven by ATP. When coupled together, the net reaction across the synthetic membrane was ATP driven sucrose transport across a flexible membrane across a closed space. As sucrose was transported, net flow of water occurred, causing pressure and deformation of the membrane. Transporters are regulated in nature. These proteins are sensitive to voltage, pH, sensitivity to a large variety of ligands and they can be modified to gain or lose these responses. Examples of sensors include ligand gated ion channels reconstituted on solid and permeable supports. Such sensors have value as high throughput screening devices for drug screening. Other sensors that have been developed in the laboratory include sensors for membrane active bacterial products such as the anthrax pore protein. These materials can be self assembled or manufactured by simple techniques, allowing the components to be stored in a stable form for years before (self) assembly on demand. The components can be modified at the atomic level, and are composed of nanostructures. Ranges of sizes of structures using these components range from the microscopic to macroscopic scale. The transport proteins can be obtained from natural sources or can be produced by recombinant methods from the genomes of all kingdoms including archea, bacteria and eukaryotes. For example, the laboratory is currently studying an ion channel from a thermophile from deep sea vents which has a growth optimum of 90 degrees centigrade, and has membrane transport proteins with very high temperature stability. The transport proteins can also be genetically modified to produce new properties such as activation by different ligands or transport of new substances such as therapeutic agents. The structures of many of these proteins are known, allowing computational chemists to help understand and predict the transport processes and to guide the engineering of new properties for the transport proteins and the composite membranes. Supported by DARPA and USARMY MURI Award and AFOSR.
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