1. |
|
|
2. |
|
|
3. |
|
|
4. |
|
|
5. |
|
|
6. |
- Andersson, Håkan S
(författare)
-
Towards the Rational Design of Molecularly Imprinted Polymers
- 1999
-
Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Molecular imprinting is a technique by which polymeric materials selective for a given target molecule can be created through a casting procedure. Functionalised monomers are added to a solution of molecular templates. Monomer-template complexes are formed and subsequently fixed through polymerisation, and following removal of the template species from the resultant molecularly imprinted polymer, MIP, a material containing binding sites able to specifically rebind the template is left. The objective of the present work has been to learn more about the mechanisms leading to the formation of selective binding sites in MIPs and the nature of these sites (1-3), with the goal to utilise this knowledge to develop better MIPs (4-7). 1) UV spectroscopic studies of the pre-polymerisation mixture were utilised to estimate the stabilities of monomer-template complexes under different conditions. It was observed that many templates are not fully complexed by monomers, possibly leading to different binding site populations. Such heterogeneity is indeed observed in MIPs. The method developed was found useful for rapid evaluation of different monomers or conditions for a given template. 2) Chromatographic studies were performed on polymers imprinted with various pyridyl templates. It was demonstrated that electrostatic interactions were those mainly responsible for binding in these systems. It was also demonstrated that free rotors in the template structure affected binding and selectivity negatively, and that the accessibilities of functional groups were essential for the utility of the template for molecular imprinting. 3) Load capacity studies of nicotine and 4,4´-bipyridyl MIPs revealed two different behaviours. The retention of 4,4´-bipyridyl decreased upon raising the sample load, but nicotine exhibited an increase. Two possible explanations to this unexpected effect were suggested: mobile phase related nicotine solvation effects or a type of cooperative binding. A maximum in resolution for the separation of (+/-)-nicotine at different sample loads indicated the presence of recognition sites for template-template complexes, implying the possible imprinting of template-template complexes. 4) A chiral tartaric acid based monomer was synthesised and employed for the imprinting of cinchona alkaloids. The chirality of the monomer was shown able to enhance selectivity for certain templates. Post-polymerisation debenzylation of the MIP enhanced both retention and selectivity due to a change from hydrogen bond interactions to ionic interactions. 5) Crown ethers were employed as co-templates in molecular imprinting to demonstrate a principle by which organic solvent non-solubles can be solubilised, and imprinted, in organic media. Rebinding studies in the absence of crown ether revealed imprinting related selectivity. 6) Imprinting in water was achieved through the introduction of a hydrophilic cross-linker, a highly acidic monomer, and a beta-cyclodextrin based monomer, able to interact by hydrophobic interactions with aromatic ring structures. By this approach, the enantiomers of phenylalanine were successfully imprinted. 7) A series of monomer combinations were evaluated to optimise the polymer system described in (6). Binding site hydrophobicities were examined by fluorescence spectroscopy. This thesis demonstrates that there is significant room for improving the performance of MIPs and points to some ways by which this can be achieved.
|
|
7. |
|
|
8. |
- Carlsson, Fredrik, 1974-, et al.
(författare)
-
Testing the probability of finding major decomposing basidiomycetes in logs with T-RFLP - implications for field sampling
-
Annan publikation (övrigt vetenskapligt/konstnärligt)abstract
- In this article we examine the limitations and potential of T-RFLP for the accurate detection of fungal species in dead wood. We collected cross-sections of decayed logs to evaluate the number of fungal species domains that are likely to be hit when drilling a sawdust sample from a log. We used these estimates to simulate the number of species that would be found using a certain number of samples. We found that in 99% of the simulations, 4 or fewer species would be contained in a sample. Based on these results we tested the probability of detecting two species of wood-decaying basidiomycetes at three different DNA concentration ratios: 1:1, 1:5 and 1:20. An additional experiment was done with 3-5 species. It was possible to detect all species at ratios higher than 1:20 but lower than 1:5; in this range all peaks were easily detected. We were able to detect all species in the mixtures of 3-5 species, with extracts from both pure cultures and wood.
|
|
9. |
|
|
10. |
- Koch, Christin, et al.
(författare)
-
CHIC - An automated approach for the detection of dynamic variations in complex microbial communities
- 2013
-
Ingår i: Cytometry Part A. - : Wiley. - 1552-4922 .- 1552-4930. ; 83A:6, s. 561-567
-
Tidskriftsartikel (refereegranskat)abstract
- Altering environmental conditions change structures of microbial communities. These effects have an impact on the single-cell level and can be sensitively detected using community flow cytometry. However, although highly accurate, microbial monitoring campaigns are still rarely performed applying this technique. One reason is the limited access to pattern analysis approaches for the evaluation of microbial cytometric data. In this article, a new analyzing tool, Cytometric Histogram Image Comparison (CHIC), is presented, which realizes trend interpretation of variations in microbial community structures (i) without any previous definition of gates, by working (ii) person independent, and (iii) with low computational demand. Various factors influencing a sensitive determination of changes in community structures were tested. The sensitivity of this technique was found to discriminate down to 0.5% internal variation. The final protocol was exemplarily applied to a complex microbial community dataset, and correlations to experimental variation were successfully shown.
|
|
11. |
- Zuntini, Alexandre R., et al.
(författare)
-
Phylogenomics and the rise of the angiosperms
- 2024
-
Ingår i: NATURE. - 0028-0836 .- 1476-4687. ; 629, s. 843-850
-
Tidskriftsartikel (refereegranskat)abstract
- Angiosperms are the cornerstone of most terrestrial ecosystems and human livelihoods(1,2). A robust understanding of angiosperm evolution is required to explain their rise to ecological dominance. So far, the angiosperm tree of life has been determined primarily by means of analyses of the plastid genome(3,4). Many studies have drawn on this foundational work, such as classification and first insights into angiosperm diversification since their Mesozoic origins(5-7). However, the limited and biased sampling of both taxa and genomes undermines confidence in the tree and its implications. Here, we build the tree of life for almost 8,000 (about 60%) angiosperm genera using a standardized set of 353 nuclear genes(8). This 15-fold increase in genus-level sampling relative to comparable nuclear studies(9) provides a critical test of earlier results and brings notable change to key groups, especially in rosids, while substantiating many previously predicted relationships. Scaling this tree to time using 200 fossils, we discovered that early angiosperm evolution was characterized by high gene tree conflict and explosive diversification, giving rise to more than 80% of extant angiosperm orders. Steady diversification ensued through the remaining Mesozoic Era until rates resurged in the Cenozoic Era, concurrent with decreasing global temperatures and tightly linked with gene tree conflict. Taken together, our extensive sampling combined with advanced phylogenomic methods shows the deep history and full complexity in the evolution of a megadiverse clade.
|
|