Trade-offs between chemical defence and regrowth capacity in Plantago lanceolata

Resistance and tolerance are different strategies of plants to deal with herbivore attack. Since resources are limited and resistance and tolerance serve similar functions for plants, trade-offs between these two strategies have often been postulated. In this study we investigated trade-offs between resistance and one aspect of tolerance, the ability to regrow after defoliation. In order to minimize confounding effects of genetic background and selection history, we used offspring derived from artificial selection lines of ribwort plantain (Plantago lanceolata) that differed in their levels of leaf iridoid glycosides (IGs), allelochemicals that confer resistance to generalist herbivores, to study genetic associations with regrowth ability. We tested whether high-IG plants (1) suffer allocation costs of resistance in terms of reduced shoot and root growth, (2) have reduced regrowth ability (tolerance) after defoliation compared to low-IG plants, and (3) whether such costs are more pronounced under nutrient stress. High-IG plants produced fewer inflorescences and side rosettes than low-IG plants and showed a different biomass allocation pattern, but since neither the vegetative, nor the reproductive biomass differed between the lines, there was no evidence for a cost of IG production in terms of total biomass production under either nutrient condition. High-IG plants also did not suffer a reduced capacity to regrow shoot mass after defoliation. However, after regrowth, root mass of high-IG plants grown under nutrient-poor conditions was significantly lower than that of low-IG plants. This suggests that under these conditions shoot regrowth of high-IG plants comes at a larger expense of root growth than in low-IG plants. We speculate therefore that if there is repeated defoliation, high-IG plants may eventually fail to maintain shoot regrowth capacity and that trade-offs between resistance and tolerance in this system will show up after repeated defoliation events under conditions of low resource availability.     

Patterns of junctional communication during development of the early amphibian embryo

Cell-cell communication through gap junctions was examined in Xenopus laevis embryos between the 16-cell and early blastula stages using Lucifer Yellow, Fluorescein, lead EDTA and dicyanoargentate as probes of junctional permeability. Injections were made into cells whose position was identified with respect to the primary cleavage axis and the grey crescent. FITC dextrans revealed cytoplasmic bridges between the injected cell and its sister only. In the animal pole at the 16-cell stage at the future dorsal side of the embryo, Lucifer Yellow was frequently and extensively transferred between cells through gap junctions. At the future ventral side gap junctional transfer of Lucifer Yellow was significantly less frequent and less extensive. The asymmetry of transfer between future dorsal and ventral sides of the animal pole was more marked at the 32-cell stage. In the vegetal pole also at the 32-cell stage, a dorsoventral difference in junctional permeability to Lucifer Yellow was observed. At the 64-cell stage the transfer of Lucifer Yellow was relatively frequent between cells lying in the same radial segment in the animal pole; transfer into cells outside each segment was infrequent, except at the grey crescent. At the 128-cell stage, Lucifer transfer between future dorsal or future ventral cells in the equatorial region was infrequent. A high incidence of transfer was restored at the future dorsal side at the 256-cell stage. At the 32-cell stage, fluorescein was infrequently transferred between animal pole cells although lead EDTA moved from cell to cell with high, comparable frequency in future dorsal and ventral regions. Dicyanoargentate always transferred extensively, both at the 32- and 64-cell stages. Treatment of embryos with methylamine raised intracellular pH by 0.15 units, increased the electrical conductance of the gap junction and produced a 10-fold increase in the frequency of Lucifer Yellow transfer through gap junctions in future ventral regions of the animal pole at the 32-cell stage.     

A Spectroscopic Mechanism for Primary Olfactory Reception

A novel theory of primary olfactory reception is described.It proposes that olfactory receptors respond not to the shapeof the molecules but to their vibrations. It differs from previousvibrational theories (Dyson, Wright) in providing a detailedand plausible mechanism for biological transduction of molecularvibrations: inelastic electron tunnelling. Elements of the tunnellingspectroscope are identified in putative olfactory receptorsand their associated G-protein. Means of calculating electrontunnelling spectra of odorant molecules are described. Severalexamples are given of correlations between tunnelling spectrumand odour in structurally unrelated molecules. As predicted,molecules of very similar shape but differing in vibrationssmell different. The most striking instance is that of pureacetophenone and its fully deuterated analogue acetophenone-d₈,which smell different despite being identical in structure.This fact cannot, it seems, be explained by structure-basedtheories of odour. The evidence presented here suggests insteadthat olfaction, like colour vision and hearing, is a spectralsense. Chem. Senses 21: 773–791, 1996.     

Biocatalytic potential of laccase-like multicopper oxidases from Aspergillus niger

Background

The integration of biotechnology into chemical manufacturing has been recognized as a key technology to build a sustainable society. However, the practical applications of biocatalytic chemical conversions are often restricted due to their complexities involving the unpredictability of product yield and the troublesome controls in fermentation processes. One of the possible strategies to overcome these limitations is to eliminate the use of living microorganisms and to use only enzymes involved in the metabolic pathway. Use of recombinant mesophiles producing thermophilic enzymes at high temperature results in denaturation of indigenous proteins and elimination of undesired side reactions; consequently, highly selective and stable biocatalytic modules can be readily prepared. By rationally combining those modules together, artificial synthetic pathways specialized for chemical manufacturing could be designed and constructed.

Results

A chimeric Embden-Meyerhof (EM) pathway with balanced consumption and regeneration of ATP and ADP was constructed by using nine recombinant E. coli strains overproducing either one of the seven glycolytic enzymes of Thermus thermophilus, the cofactor-independent phosphoglycerate mutase of Pyrococcus horikoshii, or the non-phosphorylating glyceraldehyde-3-phosphate dehydrogenase of Thermococcus kodakarensis. By coupling this pathway with the Thermus malate/lactate dehydrogenase, a stoichiometric amount of lactate was produced from glucose with an overall ATP turnover number of 31.

Conclusions

In this study, a novel and simple technology for flexible design of a bespoke metabolic pathway was developed. The concept has been testified via a non-ATP-forming chimeric EM pathway. We designated this technology as “synthetic metabolic engineering”. Our technology is, in principle, applicable to all thermophilic enzymes as long as they can be functionally expressed in the host, and thus would be potentially applicable to the biocatalytic manufacture of any chemicals or materials on demand.