Statistic thermodynamic analysis of fructans – Part 2: Chain configuration parameters of non-branched and branched fructans – Branching structure and molar mass distribution of branched fructans

2013 ◽  
pp. 219-224 ◽  
Author(s):  
Roland H.F. Beck ◽  
Anton Huber

Applying statistical thermodynamic models for chain configurations in combination with linkage analysis, molar mass distribution and small angle X-ray scattering data allow the unambiguous structural elucidation of branched fructans. The radius of gyration of fructans can be accurately predicted by applying a random flight model with bond angle restrictions. The structural factor g has been calculated and correlated with experimental data only allowing a comb shaped structure for branched fructans. A formula for calculating the molar mass distribution of comb shaped branched fructans is proposed. Amalgamation of experimental and theoretical data prove a regular comb shape structure for the branched fructans of U. maritima, L. bulbiferum and A. tequilana.

1989 ◽  
Vol 54 (7) ◽  
pp. 1821-1829
Author(s):  
Bedřich Porsch ◽  
Simon King ◽  
Lars-Olof Sundelöf

The differences between the QELSS and classical diffusion coefficient of a polydisperse polymer resulting from distinct definitions of experimentally accessible average values are calculated for two assumed specific forms of molar mass distributions. Predicted deviations are compared with the experiment using NBS 706 standard polystyrene. QELSS Dz of this sample relates within 2-4% to the classical diffusion coefficient, if the Schulz-Zimm molar mass distribution is assumed to be valid. In general, differences between the height-area and QELSS diffusion coefficient of about 20% may be found for Mw/Mn ~ 2, and this value may increase above 35%, if strongly tailing molar mass distribution pertains to the sample.


2019 ◽  
Vol 89 (23-24) ◽  
pp. 5067-5075 ◽  
Author(s):  
Helena Wedin ◽  
Marta Lopes ◽  
Herbert Sixta ◽  
Michael Hummel

The aim of this study is to improve the understanding of which end-of-life cellulosic textiles can be used for chemical recycling according to their composition, wear life and laundering—domestic versus service sector. For that purpose, end-of-life textiles were generated through laboratorial laundering of virgin fabrics under domestic and industrial conditions, and the cellulose content and its intrinsic viscosity and molar mass distribution were measured in all samples after two, 10, 20, and 50 laundering cycles. Results presented herein also address the knowledge gap concerning polymer properties of end-of-life man-made cellulosic fabrics—viscose and Lyocell. The results show that post-consumer textiles from the home consumer sector, using domestic laundering, can be assumed to have a similar, or only slightly lower, degree of polymerization than the virgin textiles (−15%). Post-consumer textiles from the service sector, using industrial laundering, can be assumed to have a substantially lower degree of polymerization. An approximate decrease of up to 80% of the original degree of polymerization can be expected when they are worn out. A higher relative decrease for cotton than man-made cellulosic textiles is expected. Furthermore, in these laboratorial laundering trials, no evidence evolved that the cellulose content in blended polyester fabrics would be significantly affected by domestic or industrial laundering. With respect to molar mass distribution, domestic post-consumer cotton waste seems to be the most suitable feedstock for chemical textile recycling using Lyocell-type processes, although a pre-treatment step might be required to remove contaminants and lower the intrinsic viscosity to 400–500 ml/g.


1995 ◽  
Vol 196 (10) ◽  
pp. 3187-3196 ◽  
Author(s):  
Emo Chiellini ◽  
Giancarlo Galli ◽  
Maria Chiara Bignozzi ◽  
Sante A. Angeloni ◽  
Marco Fagnani ◽  
...  

2018 ◽  
Vol 149 ◽  
pp. 78-84 ◽  
Author(s):  
Armando F. Reano ◽  
Alain Guinault ◽  
Emmanuel Richaud ◽  
Bruno Fayolle

2013 ◽  
Vol 33 (2) ◽  
Author(s):  
Wuan Geok Saw ◽  
Birgit Eisenhaber ◽  
Frank Eisenhaber ◽  
Gerhard Grüber

The GPI (glycosylphosphatidylinositol) transamidase complex catalyses the attachment of GPI anchors to eukaryotic proteins in the lumen of ER (endoplasmic reticulum). The Saccharomyces cerevisiae GPI transamidase complex consists of the subunits yPIG-K (Gpi8p), yPIG-S (Gpi17p), yPIG-T (Gpi16p), yPIG-U (CDC91/GAB1) and yGPAA1. We present the production of the two recombinant proteins yGPAA170–247 and yGPAA170–339 of the luminal domain of S. cerevisiae GPAA1, covering the amino acids 70–247 and 70–339 respectively. The secondary structural content of the stable and monodisperse yGPAA170–247 has been determined to be 28% α-helix and 27% β-sheet. SAXS (small-angle X-ray scattering) data showed that yGPAA170–247 has an Rg (radius of gyration) of 2.72±0.025 nm and Dmax (maximum dimension) of 9.14 nm. These data enabled the determination of the two domain low-resolution solution structure of yGPAA170–247. The large elliptical shape of yGPAA170–247 is connected via a short stalk to the smaller hook-like domain of 0.8 nm in length and 3.5 nm in width. The topological arrangement of yGPAA170–247 will be discussed together with the recently determined low-resolution structures of yPIG-K24–337 and yPIG-S38–467 from S. cerevisiae in the GPI transamidase complex.


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