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Hanning, K. R.

Publications and source records attributed to Hanning, K. R..

2 recordsLinked to original sources

GT61 β-1,2-xylosyltransferases define a conserved xylan modification in gymnosperm and Arabidopsis primary cell walls

Plant primary and secondary cell walls differ in molecular composition, structure, and mechanical properties. While secondary wall xylan has been extensively characterised, the structure of xylan in primary walls remains less well understood, particularly in gymnosperms. Here, we identify a previously uncharacterised {beta}-1,2-linked xylosyl side chain in conifer and Arabidopsis thaliana xylan. Using enzymatic fingerprinting, NMR, and mass spectrometry, we show that this structure is positioned two xylose residues away from glucuronic acid substitutions, forming an evenly patterned substituted xylan. This spacing pattern is consistent with xylan-cellulose interaction, suggesting a structural role in primary wall architecture. This modification, found in primary wall-rich tissues of diverse conifer species, including needles and pro-embryogenic mass (PEM), is also present in Arabidopsis callus. We demonstrate that conifer Group III GT61 glycosyltransferases introduce this modification with consistent positional specificity. In Arabidopsis, three closely related GT61 enzymes act redundantly to generate the same structure, and their combined loss results in its complete absence. These findings uncover a conserved primary wall xylan modification in seed plants and define the GT61 enzymes responsible for its biosynthesis, opening new avenues to explore how xylan structure contributes to primary wall function. Significance StatementXylan structure is well characterised in secondary walls, but its primary wall counterpart remains poorly understood. We identified a conserved {beta}-1,2-xylosyl modification on xylan in the primary walls of conifers and Arabidopsis. This side chain is positioned at a defined position from a glucuronic acid substitution and is introduced by GT61 glycosyltransferases that cluster in one phylogenetic subclade. Our findings revealed a previously unrecognised xylan structural pattern and the biosynthetic enzymes responsible for its addition. This work expands the current understanding of primary wall architecture across seed plants.

plant biology↗

Simple high-throughput encoding of deep mutational scanning libraries by oligo-based Golden Gate assembly

Control over mutational library diversity is an essential consideration when engineering proteins, but is often fraught with trade-offs between diversity, specificity, and affordability. Contemporary library assembly approaches often incorporate oligonucleotide pool synthesis to achieve affordable, precise mutagenesis; however, these oligos are often reliant on complex designs to facilitate downstream PCR and/or restriction digests. Direct hybridisation of oligo pools is an overlooked strategy to simplify mutagenesis, especially when paired with a type IIS restriction cloning approach. We validate this approach by designing, hybridising, and deep sequencing single and dual substitution CDR region parts derived from nanobody GA10. Assembly of these parts into a full-length nanobody CDS facilitated the phage display of variant libraries for affinity maturation against its cyclic peptide target. Variants identified through enrichment analysis were expressed in isolation and yielded improved affinities by more than 100-fold. Recent advances in machine learning have successfully inferred improved variants outside of screened library space, but require controlled, multi-mutant libraries. The library assembly approach outlined in this research is well-suited for such approaches.

synthetic biology↗