A microbial sensor for discovering structural probes of protein misfolding and aggregation

In all cell types, protein homeostasis, or “proteostasis,” is maintained by sophisticated quality control networks that regulate protein synthesis, folding, trafficking, aggregation, disaggregation, and degradation. In one notable example, Escherichia coli employ a proteostasis system that determines whether substrates of the twin-arginine translocation (Tat) pathway are correctly folded and thus suitable for transport across the tightly sealed cytoplasmic membrane. Herein, we review growing evidence that the Tat translocase itself discriminates folded proteins from those that are misfolded and/or aggregated, preferentially exporting only the former. Genetic suppressors that inactivate this mechanism have recently been isolated and provide direct evidence for the participation of the Tat translocase in structural proofreading of its protein substrates. We also discuss how this discriminatory “folding sensor” has been exploited for the discovery of structural probes (e.g., sequence mutations, pharmacologic chaperones, intracellular antibodies) that modulate the folding and solubility of virtually any protein-of-interest, including those associated with aggregation diseases (e.g., α-synuclein, amyloid-β protein). Taken together, these studies highlight the utility of engineered bacteria for rapidly and inexpensively uncovering potent anti-aggregation factors.     

Homodimerization as a molecular switch between low and high efficiency PrPC cell surface delivery and neuroprotective activity

PrP^C is associated with a variety of functions, and its ability to interact with a multitude of partners, including itself, may largely explain PrP multifunctionality and the lack of consensus on the genuine physiological function of the protein in vivo. In contrast, there is a consensus in the literature that alterations in PrP^C trafficking and intracellular retention result in neuronal degeneration. In addition, a proteolytic modification in the late secretory pathway termed the α-cleavage induces the secretion of PrPN1, a PrP^C-derived metabolite with fascinating neuroprotective activity against toxic oligomeric Aβ molecules implicated in Alzheimer disease. Thus, studies focusing on understanding the regulation of PrP^C trafficking to the cell surface and the modulation of α-cleavage are essential. The objective of this commentary is to highlight recent evidences that PrP^C homodimerization stimulates trafficking of the protein to the cell surface and results in high levels of PrPN1 secretion. We also discuss a hypothetical model for these results and comment on future challenges and opportunities.     

High-level production of Serratia proteamaculans metalloprotease using a recombinant ABC protein exporter-mediated secretion system in Pseudomonas fluorescens

Serratia proteamaculans metalloprotease (SPP) was successfully secreted by a heterologous ABC protein exporter, the Pseudomonas fluorescens TliDEF, in recombinant host strains. Escherichia coli and P. fluorescens cells containing the SPP-encoding gene showed the extracellular protease activity only when the TliDEF-encoding gene cluster was coexpressed. Recombinant P. fluorescens produced an approximately 34.8-fold higher amount of extracellular SPP than did E. coli. The use of a more nutrient-rich medium and controlled dissolved oxygen conditions was effective in increasing SPP secretion in P. fluorescens batch fermentation (an 8.7-fold increase from 41.8 U/mL to 365.2 U/mL). Therefore, SPP, which could not be secreted without an ABC protein exporter, was produced in large quantities by applying the heterologous TliDEF exporter in P. fluorescens. The results also suggest that the use of the ABC protein exporter in P. fluorescens could be an efficient production platform for an industrially promising type I secretion pathway-dependent enzyme.     

Branched-chain constituents of Brussels sprout wax

The presence of a substantial proportion of branched, in addition to normal compounds, was confirmed in the alkyl ester and primary alcohol components     

Chemotaxonomical relationships between penguins and tubenoses

The compositions of the uropygial gland wax of seven species of birds of the order Procellariiformes (tubenoses) belonging to four different families are compared with one another and with those of birds belonging to other orders. The results are discussed from a chemotaxonomical viewpoint. For this purpose, the various parameters have been depicted on a 3-dimensional matrix. Although all birds investigated are obviously related to each other, two of the species (Diomedea and Garrodia) also show a relationship to different orders. The results support the opinion that the Procellariiformes are closely related to the Sphenisciformes (penguins).     

Tarsal taste sensilla of the autumn gum moth, Mnesampela privata: morphology and electrophysiological activity

Mnesampela privata Guenée (Lepidoptera: Geometridae: Ennominae) is a native Australian geometrid that conducts considerable host assessment prior to ovipositing on its host plants, which belong to the genus Eucalyptus . The leaves of some of their hosts are covered with a particularly thick and waxy cuticle and we have shown that epicuticular waxes influence the oviposition preferences of females. This necessitates that M. privata has evolved specific chemosensory organs to assess the identity and perhaps even the quality of its hosts. In this work, we examined the morphology of tarsal taste sensilla and the sensitivity of their sensory neurones to a range of primary metabolites possibly influential on host assessment and oviposition. The ventral surface of the fifth tarsomere of females bear two parallel rows of up to eight sensilla, each loosely aligned with two parallel rows of five spines. Salts, sugars, and amino acids elicited phasi-tonic multicellular neuronal responses of variable magnitude and form. Two pairs of sensilla are closely apposed to the most distal spine in each row; the sensory neurones associated with these sensilla exhibited notably larger responses to alanine and serine compared with those of all other sensilla. The arrangement of the taste sensilla in close proximity to prominent tarsal spines is unique and could represent an adaptation that enables them to penetrate the wax layer and be brought into contact with primary metabolites present closer to the leaf surface.     

Nonacosane-5,8-diol: A new component of plant waxes

A new fraction has been isolated by chromatographic methods from the wax of the Bulgarian oil-bearing rose. According to its IR, NMR and MS it was characterized as an homologous series of γ-diols, from C¹⁷ to C³³ with the major homologues those containing an odd number of carbon atoms. Nonacosane-5,8-diol is the major constituent.     

Epicuticular wax of Cirsium arvense

Epicuticular wax of Cirsium arvense contains hydrocarbons (12%), esters (35%), free acids (3%), free alcohols (10%), triterpene acetates (8%) and 1,3-ditetradecanoyl-2-hexanoylglycerol (8%) as major components. Minor components are triterpene alcohols (3%) and nonacosan-10-ol (2%). The esters contain triterpene alcohol esters (19%) as well as esters of alkanols.     

Volatiles from the epicuticular wax of watercress (Rorippa nasturtium-aquaticum)

Volatiles from the epicuticular wax of watercress were collected by ether washing and examined using gas chromatographic and mass spectrometric analysi     

3种渗透剂对转基因烟草根系枯草芽孢杆菌纤溶酶(BSFE)分泌的调节

用0.05%～8.00%的甘露醇、山梨醇和聚乙二醇6000等3种渗透调节剂可提高转枯草芽孢杆菌纤溶酶(Bacillus subtilis fibrinolytic enzyme, BSFE)转基因烟草(Nicotiana tabacum L.)根系BSFE的分泌表达水平,其水培液BSFE活性在15 d内基本呈抛物线型变化趋势.经3种渗透剂处理后转BSFE基因烟草水培液的BSFE活性峰值明显高于对照,且出现时间比对照相对延迟1-2d.甘露醇、山梨醇和聚乙二醇6000可作为该转基因烟草根系BSFE分泌表达的有效化学调节剂.