13 research outputs found
Rhizosphere communication of plants, parasitic plants and AM fungi
Plants use an array of secondary metabolites to defend themselves against harmful organisms and to attract others that are beneficial. However, the attraction of beneficial organisms could also lead to abuse by malevolent organisms. An exciting example of such abuse is the relationship between plants, beneficial mutualistic arbuscular mycorrhizal fungi and harmful parasitic plants. Signalling molecules called strigolactones, which are secreted by plant roots in low concentrations, induce the growth of both obligate biotrophs. Here, we review the importance of strigolactones for these two interactions and discuss possible developments that should further clarify the role of these signalling molecules in rhizosphere processes
An evolutionarily mobile antigen receptor variable region gene: Doubly rearranging NAR-TcR genes in sharks
Distinctive Ig and T cell receptor (TcR) chains define the two major lineages of vertebrate lymphocyte yet similarly recognize antigen with a single, membrane-distal variable (V) domain. Here we describe the first antigen receptor chain that employs two V domains, which are generated by separate VDJ gene rearrangement events. These molecules have specialized “supportive” TcRδV domains membrane-proximal to domains with most similarity to IgNAR V. The ancestral NAR V gene encoding this domain is hypothesized to have recombined with the TRD locus in a cartilaginous fish ancestor >200 million years ago and encodes the first V domain shown to be used in both Igs and TcRs. Furthermore, these data support the view that γ/δ TcRs have for long used structural conformations recognizing free antigen
A workflow for bacterial metabolic fingerprinting and lipid profiling: application to Ciprofloxacin challenged Escherichia coli
The field of lipidomics focuses upon the non-targeted analysis of lipid composition, the process of which follows similar routines to those applied in conventional metabolic profiling, however lipidomics differs with respect to the sample preparation steps and chosen analytical platform applied to the sample analysis. Conventionally, lipidomics has applied analytical techniques such as direct infusion mass spectrometry and more recently reverse phase liquid chromatography–mass spectrometry, for the detection of mono-, di-, and tri-acyl glycerols, phospholipids, and other complex lipophilic species such as sterols. The field is rapidly expanding, especially with respect to the clinical sciences where it is known that changes of lipid composition, especially phospholipids, are commonly associated with many disease processes. As a proof of principle study, a small number of Escherichia coli isolates were selected on the basis of their sensitivity to a second generation fluoroquinolone antibiotic, known as Ciprofloxacin (E. coli isolates 161 and 171, non-ST131 isolates, which are resistant and sensitive respectively: E. coli isolates 160 and 173, ST131 sequence isolates which are resistant and susceptible respectively). It has been proposed that Ciprofloxacin may be a surface active drug that interacts at the surface-water interface of the phospholipid bi-layer where the head groups reside. Further, antibiotic resistance through intracellular exclusion is known to result in remodelling of the phospholipid membrane. Therefore, to study the effects of Ciprofloxacin on both susceptible and resistant bacterial strains, lipid profiling would present an informative approach. Control and antibiotic challenged cultures for each of the isolates were compared for changes in metabolite and lipid composition as detected by FT-IR spectroscopy and RP-UHPLC–MS, and appraised with a variety of chemometric data analysis approaches. The developed bacterial lipidomics workflow was deemed to be highly reproducible (with respect to the employed technical and analytical routines) and led to the detection of a large array of lipid classes as well as highlighting a range of significant lipid alterations that differed in regulation between susceptible and resistant E. coli isolates