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Danny E. Akin W. Herbert Morrison III Luanne L. Rigsby Franklin E. Barton II David S. Himmelsbach Kevin B. Hicks 《Applied biochemistry and biotechnology》2006,129(1-3):104-116
Information is presented on structure, composition, and response to enzymes of corn stover related to barriers for bioconversion
to ethanol. Aromatic compounds occurred in most tissue cell walls. Ferulic acid esterase treatment before cellulase treatment
significantly improved dry weight loss and release of phenolic acids and sugars in most fractions over cellulase alone. Leaf
fractions were considerably higher in dry weight loss and released sugars with esterase treatment, but stem pith cells gave
up the most phenolic acids. Results help identify plant fractions more appropriate for coproducts and bioconversion and those
more suitable as residues for soil erosion control. 相似文献
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Ramamurthy Charubala Eugen Uhlmann Frank Himmelsbach Wolfgang Pfleiderer 《Helvetica chimica acta》1987,70(8):2028-2038
The chemical synthesis of 3′-deoxyadenyly-(2′-5′)-3′-deoxyadenylyl-(2′-5′)-3′-deoxyadenosine ( 30 ; trimeric cordycepin) is described by three different routes using various protecting groups and applying the phosphotriester approach. The intermediates have been isolated and characterized by elemental analyses and spectroscopic means. High yields of 30 have been obtained on deprotection making this biologically very active compound available in preparative scale. 相似文献
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Tim J. Causon Markus Himmelsbach Wolfgang Buchberger Christian W. Klampfl 《Electrophoresis》2013,34(6):944-949
Polyimides (PIs) are a group of widely used synthetic materials that service a variety of different purposes including microelectronics, insulating films and aerospace applications. Depending on the requirements (defined by the particular final product), the actual composition of PIs may show substantial chemical variation. To study this variation in chemical structure, CE‐MS can be employed for the determination of PI composition following chemical degradation of the polymer sample. PI is chemically decomposed to corresponding aromatic diamine and carboxylic acid components using an alkali fusion reaction. Solid polymer samples are fused in a potassium hydroxide melt yielding reaction products that are diluted in acid and can be immediately analysed by CE coupled to a Q/TOF‐MS with quantification performed using conventional UV detection. This approach involves a simple and rapid sample preparation yielding both qualitative and quantitative information regarding the chemical composition of the polymer. Application of the CE‐MS approach is shown for a range of commercially available PI and poly(amide–imide) materials and the results are used to infer the respective chemical compositions. 相似文献
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Stephan Schaumüller Doris Cristurean Stephan Haudum George S. Pappas Markus Himmelsbach Matthias Bechmann Oliver Brüggemann Ian Teasdale 《Journal of polymer science. Part A, Polymer chemistry》2021,59(24):3161-3166
We report a facile post-polymerization modification route to functionalized aromatic polyimides via Diels-Alder cycloaddition. Aromatic polyimides are important, versatile high-performance polymers; however, their structural diversity is restricted by the requirements of the step-growth polymerization. We prepared polyimides with alkynes in their main-chain as macromolecular dienophiles and quantitatively grafted tetraphenylcyclopentadienone based dienes. The resulting solution-processable, wholly aromatic polyimides show a considerable increase in surface area due to the induced conformational changes and bulky, rigid, and contorted molecular structures. The orthogonality of the reaction is exploited to insert functional groups, namely bromine and sulfonates, along the polymer backbone. In a further extension, the phenylene segments undergo cyclodehydrogenation to form nanographene segments within the polymer chains. The Diels-Alder cycloaddition onto polyimides is therefore demonstrated to be an effective, widely applicable route to tunable high-performance polymers with value-added functionality and thus considerable potential in a wide range of advanced materials. 相似文献
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A new phosphorylating agent, bis-(p-nitrophenylethyl)phoshoromonochloridate, has been prepared and is used for 3′- and/or 5′-phosphorylations of nucleosides. The resulting bis-(p-nitrophenylethyl)phosphotriesters are versatile synthons in oligonucleotide syntheses leading finally to 3′- and/or 5′-terminated oligonucleotides in excellent yields. 相似文献
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Isci A Himmelsbach JN Strohl J Pometto AL Raman DR Anex RP 《Applied biochemistry and biotechnology》2009,157(3):453-462
Aqueous-ammonia-steeped switchgrass was subject to simultaneous saccharification and fermentation (SSF) in two pilot-scale
bioreactors (50- and 350-L working volume). Switchgrass was pretreated by soaking in ammonium hydroxide (30%) with solid to
liquid ratio of 5 L ammonium hydroxide per kilogram dry switchgrass for 5 days in 75-L steeping vessels without agitation
at ambient temperatures (15 to 33 °C). SSF of the pretreated biomass was carried out using Saccharomyces cerevisiae (D5A) at approximately 2% glucan and 77 filter paper units per gram cellulose enzyme loading (Spezyme CP). The 50-L fermentation
was carried out aseptically, whereas the 350-L fermentation was semiaseptic. The percentage of maximum theoretical ethanol
yields achieved was 73% in the 50-L reactor and 52–74% in the 350-L reactor due to the difference in asepsis. The 350-L fermentation
was contaminated by acid-producing bacteria (lactic and acetic acid concentrations approaching 10 g/L), and this resulted
in lower ethanol production. Despite this problem, the pilot-scale SSF of aqueous-ammonia-pretreated switchgrass has shown
promising results similar to laboratory-scale experiments. This work demonstrates challenges in pilot-scale fermentations
with material handling, aseptic conditions, and bacterial contamination for cellulosic fermentations to biofuels. 相似文献
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Wolfgang W. Buchberger Ingrid HattingerMarkus Himmelsbach 《Journal of chromatography. A》2009,1216(1):113-118
The polycondensation of guanidine hydrochloride and 2,2′-(ethylenedioxy)bis(ethylamine) leads to various types of oligomeric guanidines exhibiting a broad spectrum of biocidal activities. In the present work a reversed-phase high-performance liquid chromatographic method with a gradient consisting of aqueous 0.1% trifluoroacetic acid and acetonitrile as mobile phase has been developed to separate these oligoguanidines according to type and chain length. The combination with electrospray mass spectrometry allowed the identification of the various compounds. By this technique, some structures already suggested in the literature could be confirmed, and several additional oligoguanidines not yet reported could be identified. As a complementary technique, capillary zone electrophoresis was investigated. Best results were obtained with carrier electrolytes consisting of phosphoric acid in water/acetonitrile mixtures. Although the number of peaks that could be separated by the electrophoretic method was considerably lower than in case of the chromatographic method, capillary electrophoresis in combination with UV detection at 195 nm may still be a fast method suitable for quantitation of some of the major compounds and for monitoring the reaction rate during the polycondensation reaction. 相似文献