@article{ComasBruHarrisonWerneretal.2019, author = {Comas-Bru, Laia and Harrison, Sandy P. and Werner, Martin and Rehfeld, Kira and Scroxton, Nick and Veiga-Pires, Cristina and Ahmad, Syed Masood and Brahim, Yassine Ait and Mozhdehi, Sahar Amirnezhad and Arienzo, Monica and Atsawawaranunt, Kamolphat and Baker, Andy and Braun, Kerstin and Breitenbach, Sebastian Franz Martin and Burstyn, Yuval and Chawchai, Sakonvan and Columbu, Andrea and Deininger, Michael and Demeny, Attila and Dixon, Bronwyn and Hatvani, Istvan Gabor and Hu, Jun and Kaushal, Nikita and Kern, Zoltan and Labuhn, Inga and Lachniet, Matthew S. and Lechleitner, Franziska A. and Lorrey, Andrew and Markowska, Monika and Nehme, Carole and Novello, Valdir F. and Oster, Jessica and Perez-Mejias, Carlos and Pickering, Robyn and Sekhon, Natasha and Wang, Xianfeng and Warken, Sophie and Atkinson, Tim and Ayalon, Avner and Baldini, James and Bar-Matthews, Miryam and Bernal, Juan Pablo and Boch, Ronny and Borsato, Andrea and Boyd, Meighan and Brierley, Chris and Cai, Yanjun and Carolin, Stacy and Cheng, Hai and Constantin, Silviu and Couchoud, Isabelle and Cruz, Francisco and Denniston, Rhawn and Dragusin, Virgil and Duan, Wuhui and Ersek, Vasile and Finne, Martin and Fleitmann, Dominik and Fohlmeister, Jens Bernd and Frappier, Amy and Genty, Dominique and Holzkamper, Steffen and Hopley, Philip and Johnston, Vanessa and Kathayat, Gayatri and Keenan-Jones, Duncan and Koltai, Gabriella and Li, Ting-Yong and Lone, Mahjoor Ahmad and Luetscher, Marc and Mattey, Dave and Moreno, Ana and Moseley, Gina and Psomiadis, David and Ruan, Jiaoyang and Scholz, Denis and Sha, Lijuan and Smith, Andrew Christopher and Strikis, Nicolas and Treble, Pauline and Unal-Imer, Ezgi and Vaks, Anton and Vansteenberge, Stef and Voarintsoa, Ny Riavo G. and Wong, Corinne and Wortham, Barbara and Wurtzel, Jennifer and Zhang, Haiwei}, title = {Evaluating model outputs using integrated global speleothem records of climate change since the last glacial}, series = {Climate of the past : an interactive open access journal of the European Geosciences Union}, volume = {15}, journal = {Climate of the past : an interactive open access journal of the European Geosciences Union}, number = {4}, publisher = {Copernicus}, address = {G{\"o}ttingen}, organization = {SISAL Working Grp}, issn = {1814-9324}, doi = {10.5194/cp-15-1557-2019}, pages = {1557 -- 1579}, year = {2019}, abstract = {Although quantitative isotope data from speleothems has been used to evaluate isotope-enabled model simulations, currently no consensus exists regarding the most appropriate methodology through which to achieve this. A number of modelling groups will be running isotope-enabled palaeoclimate simulations in the framework of the Coupled Model Intercomparison Project Phase 6, so it is timely to evaluate different approaches to using the speleothem data for data-model comparisons. Here, we illustrate this using 456 globally distributed speleothem δ18O records from an updated version of the Speleothem Isotopes Synthesis and Analysis (SISAL) database and palaeoclimate simulations generated using the ECHAM5-wiso isotope-enabled atmospheric circulation model. We show that the SISAL records reproduce the first-order spatial patterns of isotopic variability in the modern day, strongly supporting the application of this dataset for evaluating model-derived isotope variability into the past. However, the discontinuous nature of many speleothem records complicates the process of procuring large numbers of records if data-model comparisons are made using the traditional approach of comparing anomalies between a control period and a given palaeoclimate experiment. To circumvent this issue, we illustrate techniques through which the absolute isotope values during any time period could be used for model evaluation. Specifically, we show that speleothem isotope records allow an assessment of a model's ability to simulate spatial isotopic trends. Our analyses provide a protocol for using speleothem isotope data for model evaluation, including screening the observations to take into account the impact of speleothem mineralogy on δ18O values, the optimum period for the modern observational baseline and the selection of an appropriate time window for creating means of the isotope data for palaeo-time-slices.}, language = {en} } @phdthesis{BahrkeEinarssonGislasonetal.2003, author = {Bahrke, Sven and Einarsson, Jon M. and Gislason, Johannes and Haebel, Sophie and Peter-Katalinic, Jasna and Peter, Martin G.}, title = {Characterization of chitooligosaccharides by mass spectrometry}, isbn = {82-47-15901-5}, year = {2003}, language = {en} } @misc{TsukamotoHeabelValencaetal.2008, author = {Tsukamoto, Junko and Heabel, Sophie and Valenca, Gustavo P. and Peter, Martin and Franco, Telma}, title = {Enzymatic direct synthesis of acrylic acid esters of mono- and disaccharides}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-42652}, year = {2008}, abstract = {BACKGROUND: There is an increased need to replace materials derived from fossil sources by renewables. Sugar-cane derived carbohydrates are very abundant in Brazil and are the cheapest sugars available in the market, with more than 400 million tons of sugarcane processed in the year 2007. The objective of this work was to study the preparation of sugar acrylates from free sugars and free acrylic acid, thus avoiding the previous preparation of protected sugar derivatives, such as glycosides, or activated acrylates, such as vinyl acrylate. RESULTS: Lipase catalyzed esterification of three mono- and two disaccharides with acrylic acid, in the presence or absence of molecular sieves was investigated. The reactions were monitored by high-performance liquid chromatography (HPLC) and the products were analyzed by matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometry. The main products are mono- and diacrylates, while higher esters are formed as minor products. The highest conversion to sugar acrylates was observed for the D-glucose and D-fructose, followed by D-xylose and D-maltose. Molecular sieves had no pronounced effect on the conversion CONCLUSIONS: A feasible method is described to produce and to characterize sugar acrylates, including those containing more than two acrylate groups. The process for production of these higher esters could potentially be optimized further to produce molecules for cross-linking in acrylate polymerization and other applications. The direct enzymatic esterification of free carbohydrates with acrylic acid is unprecedented.}, language = {en} } @article{GrunwaldtHaebelSpitzetal.2002, author = {Grunwaldt, Gisela and Haebel, Sophie and Spitz, Christian and Steup, Martin and Menzel, Ralf}, title = {Multiple binding sites of fluorescein isothiocyanate moieties on myoglobin : photophysical heterogeneity as revealed by ground- and excited-state spectroscopy}, issn = {1011-1344}, year = {2002}, language = {en} } @article{KehrHaebelBlechschmidtSchneideretal.1999, author = {Kehr, Julia and Haebel, Sophie and Blechschmidt-Schneider, Sabine and Willmitzer, Lothar and Steup, Martin and Fisahn, Joachim}, title = {Analysis of phloem protein patterns from different organs of Cucurbita maxima Duch. by matrix-assisted laser desorption/ionization time of flight mass spectroscopy combined with sodium dodecyl sufate-polyacryilamide gel electrophoresis}, year = {1999}, language = {en} } @article{HaebelAlbrechtSparbieretal.1998, author = {Haebel, Sophie and Albrecht, Tanja and Sparbier, Katrin and Walden, Peter and K{\"o}rner, Roman and Steup, Martin}, title = {Electrophoresis-related protein modification: alkylation of carboxy residues revealed by mass spectrometry}, year = {1998}, language = {en} } @article{RitteEckermannHaebeletal.2000, author = {Ritte, Gerhard and Eckermann, Nora and Haebel, Sophie and Lorberth, Ruth and Steup, Martin}, title = {Compartmentation of the starch-related R1 protein in higher plants}, year = {2000}, language = {en} } @article{DauvilleeChochoisSteupetal.2006, author = {Dauvillee, David and Chochois, Vincent and Steup, Martin and Haebel, Sophie and Eckermann, Nora and Ritte, Gerhard and Ral, Jean-Philippe and Colleoni, Christophe and Hicks, Glenn and Wattebled, Fabrice and Deschamps, Philippe and Lienard, Luc and Cournac, Laurent and Putaux, Jean-Luc and Dupeyre, Danielle and Ball, Steven G.}, title = {Plastidial phosphorylase is required for normal starch synthesis in Chlamydomonas reinhardtii}, series = {The plant journal}, volume = {48}, journal = {The plant journal}, number = {2}, publisher = {Blackwell}, address = {Oxford}, issn = {0960-7412}, doi = {10.1111/j.1365-313X.2006.02870.x}, pages = {274 -- 285}, year = {2006}, abstract = {Among the three distinct starch phosphorylase activities detected in Chlamydomonas reinhardtii, two distinct plastidial enzymes (PhoA and PhoB) are documented while a single extraplastidial form (PhoC) displays a higher affinity for glycogen as in vascular plants. The two plastidial phosphorylases are shown to function as homodimers containing two 91-kDa (PhoA) subunits and two 110-kDa (PhoB) subunits. Both lack the typical 80-amino-acid insertion found in the higher plant plastidial forms. PhoB is exquisitely sensitive to inhibition by ADP-glucose and has a low affinity for malto-oligosaccharides. PhoA is more similar to the higher plant plastidial phosphorylases: it is moderately sensitive to ADP-glucose inhibition and has a high affinity for unbranched malto-oligosaccharides. Molecular analysis establishes that STA4 encodes PhoB. Chlamydomonas reinhardtii strains carrying mutations at the STA4 locus display a significant decrease in amounts of starch during storage that correlates with the accumulation of abnormally shaped granules containing a modified amylopectin structure and a high amylose content. The wild-type phenotype could be rescued by reintroduction of the cloned wild-type genomic DNA, thereby demonstrating the involvement of phosphorylase in storage starch synthesis.}, language = {en} } @article{RitteHeydenreichMahlowetal.2006, author = {Ritte, Gerhard and Heydenreich, Matthias and Mahlow, Sebastian and Haebel, Sophie and Koetting, Oliver and Steup, Martin}, title = {Phosphorylation of C6- and C3-positions of glucosyl residues in starch is catalysed by distinct dikinases}, series = {FEBS letters : the journal for rapid publication of short reports in molecular biosciences}, volume = {580}, journal = {FEBS letters : the journal for rapid publication of short reports in molecular biosciences}, number = {20}, publisher = {Elsevier}, address = {Amsterdam}, issn = {0014-5793}, doi = {10.1016/j.febslet.2006.07.085}, pages = {4872 -- 4876}, year = {2006}, abstract = {Glucan, water dikinase (GWD) and phosphoglucan, water dikinase (PWD) are required for normal starch metabolism. We analysed starch phosphorylation in Arabidopsis wildtype plants and mutants lacking either GWD or PWD using P-31 NMR. Phosphorylation at both C6- and C3-positions of glucose moieties in starch was drastically decreased in GWD-deficient mutants. In starch from PWD-deficient plants C3-bound phosphate was reduced to levels close to the detection limit. The latter result contrasts with previous reports according to which GWD phosphorylates both C6- and C3-positions. In these studies, phosphorylation had been analysed by HPLC of acid-hydrolysed glucans. We now show that maltose-6-phosphate, a product of incomplete starch hydrolysis, co-eluted with glucose-3-phosphate under the chromatographic conditions applied. Re-examination of the specificity of the dikinases using an improved method demonstrates that C6- and C3-phosphorylation is selectively catalysed by GWD and PWD, respectively.}, language = {en} } @article{RitteScharfEckermannetal.2004, author = {Ritte, Gerhard and Scharf, Anke and Eckermann, Nora and Haebel, Sophie and Steup, Martin}, title = {Phosphorylation of transitory starch is increased during degradation}, year = {2004}, abstract = {The starch excess phenotype of Arabidopsis mutants defective in the starch phosphorylating enzyme glucan, water dikinase (EC 2.7.9.4) indicates that phosphorylation of starch is required for its degradation. However, the underlying mechanism has not yet been elucidated. In this study, two in vivo systems have been established that allow the analysis of phosphorylation of transitory starch during both biosynthesis in the light and degradation in darkness. First, a photoautotrophic culture of the unicellular green alga Chlamydomonas reinhardtii was used to monitor the incorporation of exogenously supplied P-32 orthophosphate into starch. Illuminated cells incorporated P-32 into starch with a constant rate during 2 h. By contrast, starch phosphorylation in darkened cells exceeded that in illuminated cells within the first 30 min, but subsequently phosphate incorporation declined. Pulse-chase experiments performed with P-32/P-31 orthophosphate revealed a high turnover of the starch-bound phosphate esters in darkened cells but no detectable turnover in illuminated cells. Secondly, leaf starch granules were isolated from potato (Solanum tuberosum) plants grown under controlled conditions and glucan chains from the outer granule layer were released by isoamylase. Phosphorylated chains were purified and analyzed using high performance anion-exchange chromatography and matrix-assisted laser desorption/ionization mass spectrometry. Glucans released from the surface of starch granules that had been isolated from darkened leaves possessed a considerably higher degree of phosphorylation than those prepared from leaves harvested during the light period. Thus, in the unicellular alga as well as in potato leaves, net starch degradation is accompanied with an increased phosphorylation of starch}, language = {en} }