24 research outputs found
The Real Versus the Financial Economy: A Global Tale of Stability Versus Volatility
The question how the real and the financial side of a capitalist economy relate to each other
has been a frequently recurring topic in the history of economic thought. Our paper addresses
this question from the viewpoint that capital ultimately seeks returns from its perpetual
reallocation and essentially faces two choices: it can either be âentrepreneuriallyâ allocated to
real economic activity, or it can be âfinanciallyâ invested in legal claims against such activity.
Adopting such a perspective, we study here how real and financial returns relate to each
other over the past fifteen years, both within and across countries, by considering more than
30,000 publicly traded firms in more than forty countries that stand for 70% of the global
population and about 90% of world income. We compare the average rates of return to both
types of investment and their respective volatilities. While average returns, perhaps somewhat
surprisingly, turn out to be roughly equal across the two domains, the volatility of financial
returns exceeds âreal volatilityâ by an order of magnitude. From a systemic point of view, these
findings raise the question why capital would seek out financial investments in the first place
Development of new USER-based cloning vectors for multiple genes expression in Saccharomyces cerevisiae
Glucose-based microbial production of the hormone melatonin in yeast <i>Saccharomyces cerevisiae</i>
Melatonin is a natural mammalian hormone that plays an important role in regulating the circadian cycle in humans. It is a clinically effective drug exhibiting positive effects as a sleep aid and a powerful antioxidant used as a dietary supplement. Commercial melatonin production is predominantly performed by complex chemical synthesis. In this study, we demonstrate microbial production of melatonin and related compounds, such as serotonin and Nâacetylserotonin. We generated Saccharomyces cerevisiae strains that comprise heterologous genes encoding one or more variants of an Lâtryptophan hydroxylase, a 5âhydroxyâLâtryptophan decarboxylase, a serotonin acetyltransferase, an acetylserotonin Oâmethyltransferase, and means for providing the cofactor tetrahydrobiopterin via heterologous biosynthesis and recycling pathways. We thereby achieved de novo melatonin biosynthesis from glucose. We furthermore accomplished increased product titers by altering expression levels of selected pathway enzymes and boosting coâfactor supply. The final yeast strain produced melatonin at a titer of 14.50 ± 0.57 mg L(â1) in a 76h fermentation using simulated fedâbatch medium with glucose as sole carbon source. Our study lays the basis for further developing a yeast cell factory for biological production of melatonin
Evolution reveals a glutathione-dependent mechanism of 3-hydroxypropionic acid tolerance
Biologically produced 3-hydroxypropionic acid (3HP) is a potential source for sustainable acrylates and can also find direct use as monomer in the production of biodegradable polymers. For industrial scale production there is a need for robust cell factories tolerant to high concentration of 3HP, preferably at low pH. Through adaptive laboratory evolution we selected S. cerevisiae strains with improved tolerance to 3HP at pH 3.5. Genome sequencing followed by functional analysis identified the causal mutation in SFA1 gene encoding S-(hyclroxymerhyl)glutathione dehydrogenase. Based on our findings, we propose that 3HP toxicity is mediated by 3-hydroxypropionic aldehyde (reuterin ) and that glutathione-dependent reactions are used for reuterin detoxification. The identified molecular response to 3HP and reuterin may well be a general mechanism for handling resistance to organic acid and aldehydes by living cells. (C) 2014 International Metabolic Engineering Society Published by Elsevier Inc. On behalf of International Metabolic Engineering Society. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/
USER-based vector set for high-throughput cloning and metabolic engineering in <i>Saccharomyces cerevisiae</i>
Engineering and systems level analysis of <i>Saccharomyces cerevisiae</i> for production of 3 hydroxypropionic acid via malonyl CoA reductase dependent pathway
Evolution Reveals A Glutathione-dependent Mechanism Of 3-hydroxypropionic Acid Detoxification
Precision and accuracy of single-molecule FRET measurements - a multi-laboratory benchmark study
Single-molecule Förster resonance energy transfer (smFRET) is increasingly being used to determine distances, structures, and dynamics of biomolecules in vitro and in vivo. However, generalized protocols and FRET standards to ensure the reproducibility and accuracy of measurements of FRET efficiencies are currently lacking. Here we report the results of a comparative blind study in which 20 labs determined the FRET efficiencies (E) of several dye-labeled DNA duplexes. Using a unified, straightforward method, we obtained FRET efficiencies with s.d. between ±0.02 andâ±0.05. We suggest experimental and computational procedures for converting FRET efficiencies into accurate distances, and discuss potential uncertainties in the experiment and the modeling. Our quantitative assessment of the reproducibility of intensity-based smFRET measurements and a unified correction procedure represents an important step toward the validation of distance networks, with the ultimate aim of achieving reliable structural models of biomolecular systems by smFRET-based hybrid methods