Nutrient limitation and botanical diversity in wetlands: can fertilisation raise species richness?

The 'resource balance hypothesis' proposes that the species richness of grassland vegetation is potentially highest when the N:P ratio of plant tissues is 10–15 (co-limitation), so that species richness could be raised by fertilisation with N or P at sites with lower or higher N:P ratios, respectively. Here we use data from field surveys in Swiss, Dutch and American fens or wet grasslands to analyse what changes in N:P ratios might produce noticeable changes in species richness. Plant species numbers, above-ground biomass, tissue N and P concentrations and soil pH were recorded in plots of 0.06–4 m². In each data set, plots with intermediate tissue N:P ratios (6–20) were on average most species-rich, but N:P ratios explained only 5–37% of the variation in species richness. Moreover, these effects were partially confounded with those of vegetation biomass and/or soil pH. The unique effects of N:P ratios (excluding those shared with biomass and pH) explained 11–17% of variation in species richness. The relationship between species richness and N:P ratios was asymmetric: plots with high N:P ratios were more species-poor than those with low N:P ratios. This was paralleled by a smaller species pool size at high N:P ratios (estimated from species numbers in multiple records), suggesting that fewer species are adapted to P-limited conditions than to N-limited conditions. According to these data, species richness in wetlands may possibly be raised by P-fertilisation when the initial N:P ratio of the vegetation is well above 20, but this option is not recommended for nature conservation as it might promote common species at the expense of rare ones.     

Copepod grazing impact on the trophic structure of the microbial assemblage of the San Pedro Channel, California

In August 2002 and March 2003 the trophic structure of the microbialassemblage from the San Pedro Channel, California was studiedfollowing the experimental alteration of the number of copepods.Changes in the abundance/biomass of microorganisms <80 µmduring 3-day incubations were monitored in (i) the absence ofmetazoa >80 µm, (ii) the presence of natural abundancesof metazoa and (iii) the presence of an elevated number of copepods.Prokaryotes and small-sized eukaryotes (<4 µm) dominatedplankton biomass during both experimental months. Diatoms numericallydominated the 10–80 µm plankton in August 2002,but ciliate and heterotrophic dinoflagellate biomass generallyexceeded diatom biomass on both dates. Ingestion of protozooplankton(predominantly ciliates) contributed substantially to copepoddaily carbon rations. The adult copepod assemblage removed 4.6and 36% per day of the microzooplankton standing stocks (10–80µm size fraction) in August and March, respectively. Elevatedcopepod grazing pressure on protozooplankton resulted in increasedbiomass of nanoplankton (<5 µm) presumably via a trophiccascade. Accordingly, the copepod–protozoan trophic linkappears to be a key factor structuring the planktonic microbialassemblage in the San Pedro Channel. This paper is one of six on the subject of the role of zooplanktonpredator–prey interactions in structuring plankton communities.     

Proteomic Profiling of Recombinant Escherichia coli in High-Cell- Density Fermentations for Improved Production of an Antibody Fragment Biopharmaceutical

By using two-dimensional polyacrylamide gel electrophoresis, a proteomic analysis over time was conducted with high-cell-density, industrial, phosphate-limited Escherichia coli fermentations at the 10-liter scale. During production, a recombinant, humanized antibody fragment was secreted and assembled in a soluble form in the periplasm. E. coli protein changes associated with culture conditions were distinguished from protein changes associated with heterologous protein expression. Protein spots were monitored quantitatively and qualitatively. Differentially expressed proteins were quantitatively assessed by using a t-test method with a 1% false discovery rate as a significance criterion. As determined by this criterion, 81 protein spots changed significantly between 14 and 72 h (final time) of the control fermentations (vector only). Qualitative (on-off) comparisons indicated that 20 more protein spots were present only at 14 or 72 h in the control fermentations. These changes reflected physiological responses to the culture conditions. In control and production fermentations at 72 h, 25 protein spots were significantly differentially expressed. In addition, 19 protein spots were present only in control or production fermentations at this time. The quantitative and qualitative changes were attributable to overexpression of recombinant protein. The physiological changes observed during the fermentations included the up-regulation of phosphate starvation proteins and the down-regulation of ribosomal proteins and nucleotide biosynthesis proteins. Synthesis of the stress protein phage shock protein A (PspA) was strongly correlated with synthesis of a recombinant product. This suggested that manipulation of PspA levels might improve the soluble recombinant protein yield in the periplasm for this bioprocess. Indeed, controlled coexpression of PspA during production led to a moderate, but statistically significant, improvement in the yield.     

A step-wise approach significantly enhances protein yield of a rationally-designed agonist antibody fragment in E. coli

Fab59 is a rationally-designed antibody fragment (Fab) that mimics the activity of the cytokine thrombopoietin (TPO). Fab59 activity was initially detected directly from bacterial supernatants in a cell-based assay and was subsequently estimated to be equipotent to TPO using purified material. However, the expression of Fab59 was insufficient to support in vivo characterization of the Fab due to extremely low expression levels from its initial phage display expression vector. To boost expression, a new expression vector was designed and constructed, and Fab59 light chain codons were optimized for bacterial expression. However, from this a new challenge arose, in that the codon-optimized Fab59 was more toxic to Escherichia coli cells than parental Fab59. Co-expression of the bacterial chaperon protein Skp alleviated this toxicity. A two-step purification method was used to isolate monomeric Fab59 from the periplasm. Although Fab59 was prone to form aggregates during the purification process, buffer modification efficiently eliminated this problem. Overall, optimization of Fab59 expression and purification achieved a 100-fold increase in Fab59 production in E. coli relative to the starting yield. The yield of purified monomeric Fab59 from a shake flask reached up to 3.5mg/L, which was sufficient to support testing of the agonist activity of purified monomeric Fab59 in vivo. Even higher yields may be achieved by purification of Fab present in the culture media, as Skp most significantly increased accumulation of Fab59 in that location.     

cIAP1 and cIAP2 facilitate cancer cell survival by functioning as E3 ligases that promote RIP1 ubiquitination

The inhibitor of apoptosis (IAP) family of proteins enhances cell survival through mechanisms that remain uncertain. In this report, we show that cIAP1 and cIAP2 promote cancer cell survival by functioning as E3 ubiquitin ligases that maintain constitutive ubiquitination of the RIP1 adaptor protein. We demonstrate that AEG40730, a compound modeled on BIR-binding tetrapeptides, binds to cIAP1 and cIAP2, facilitates their autoubiquitination and proteosomal degradation, and causes a dramatic reduction in RIP1 ubiquitination. We show that cIAP1 and cIAP2 directly ubiquitinate RIP1 and induce constitutive RIP1 ubiquitination in cancer cells and demonstrate that constitutively ubiquitinated RIP1 associates with the prosurvival kinase TAK1. When deubiquitinated by AEG40730 treatment, RIP1 binds caspase-8 and induces apoptosis. These findings provide insights into the function of the IAPs and provide new therapeutic opportunities in the treatment of cancer.