Biology subjects

Atkinson, S. C.

Publications and source records attributed to Atkinson, S. C..

4 recordsLinked to original sources

bioRxiv2021

Language barriers in global bird conservation

Multiple languages being spoken within a species distribution can impede communication among conservation stakeholders, the compilation of scientific information, and the development of effective conservation actions. Here, we investigate the number of official languages spoken within the distributions of 10,863 bird species to identify which ones might be particularly affected by consequences of language barriers. We show that 1587 species have 10 languages or more spoken within their distributions. Threatened, migratory and wide-ranging species have especially many languages spoken within their distribution. Particularly high numbers of species with many languages within their distribution are found in Eastern Europe, Russia and central and western Asia. Global conservation efforts would benefit from implementing guidelines to overcome language barriers, especially in regions with high species and language diversity.

ecology↗

bioRxiv2020

Metal Dependent Dynamic Equilibrium: A Regulatory Mechanism for M17 Aminopeptidases from Plasmodium falciparum and Plasmodium vivax

M17 leucyl aminopeptidases are metal-dependent exopeptidases that rely on oligomerization to diversify their functional roles. The M17 aminopeptidases from Plasmodium falciparum (PfA-M17) and Plasmodium vivax (Pv-M17) function as catalytically active hexamers to acquire free amino acids from human hemoglobin and are drug targets for the design of novel anti-malarial agents. In this study, we found that the active site metal ions essential for catalytic activity have a secondary structural role mediating the formation of active hexamers. We found that PfA-M17 and Pv-M17 exist in a metal-dependent dynamic equilibrium between active hexameric species and smaller inactive species, that can be controlled by manipulating the identity and concentration of metal ions available. Mutation of residues involved in metal ion binding impaired catalytic activity and the formation of active hexamers. Structural resolution of the Pv-M17 hexameric species revealed that PfA-M17 and Pv-M17 bind metal ions and substrates in a conserved fashion, although Pv-M17 forms the active hexamer more readily and processes substrates faster than PfA-M17. On the basis of solution studies and structures determined by cryo-electron microscopy, we propose a dynamic equilibrium between monomer dimer tetramer hexamer, which becomes directional towards the large oligomeric states with the addition of metal ions. M17 aminopeptidases can exploit this sophisticated metal-dependent dynamic equilibrium to regulate formation of the catalytically active hexamer and therefore regulate catalysis.

biochemistry↗

bioRxiv2019

Conservation attention necessary across at least 44% of Earth’s terrestrial area to safeguard biodiversity

More ambitious conservation efforts are needed to stop the global biodiversity crisis. Here, we estimate the minimum land area to secure important sites for terrestrial fauna, ecologically intact areas, and the optimal locations for representation of species ranges and ecoregions. We discover that at least 64 million km2 (44% of terrestrial area) requires conservation attention. Over 1.8 billion people live on these lands so responses that promote agency, self-determination, equity, and sustainable management for safeguarding biodiversity are essential. Spatially explicit land-use scenarios suggest that 1.3 million km2 of land requiring conservation could be lost to intensive human land-uses by 2030, which requires immediate attention. However, there is a seven-fold difference between the amount of habitat converted under optimistic and pessimistic scenarios, highlighting an opportunity to avert this crisis. Appropriate targets in the post-2020 Global Biodiversity Framework to ensure conservation of the identified land would contribute substantially to safeguarding biodiversity.

ecology↗

bioRxiv2018

The specificity of ParR binding determines the compatibility of conjugative plasmids in Clostridium perfringens

Plasmids that encode the same replication machinery are generally unable to coexist in the same bacterial cell. However, Clostridium perfringens strains often carry multiple conjugative toxin or antibiotic resistance plasmids that are closely related and encode similar Rep proteins. In many bacteria, plasmid partitioning upon cell division involves a ParMRC system and there are ~10 different ParMRC families in C. perfringens, with differences in amino acid sequences between each ParM family (15% - 54% identity). Since plasmids encoding genes belonging to the same ParMRC family are not observed in the same strain, these families appear to represent the basis for plasmid compatibility in C. perfringens. To understand this process, we examined the key recognition steps between ParR DNA-binding proteins and their parC binding sites. The ParR proteins bound to sequences within a parC site from the same ParMRC family, but could not interact with a parC site from a different ParMRC family. These data provide evidence that compatibility of the conjugative toxin plasmids of C. perfringens is mediated by their parMRC-like partitioning systems. This process provides a selective advantage by enabling the host bacterium to maintain separate plasmids that encode toxins that are specific for different host targets.

microbiology↗