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Team:Wageningen UR/Engineering morphology
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Anderson and Smith found that at 44C germ-tube formation was completely inhibited in Aspergillus niger, although spherical growth could occur over a prolonged period to produce large spherical cells. More generally, there are more dimorphic fungi that display such a distinctive phenotypic transition at elevated temperatures. This made us ponder and let to the idea of generating a single cellular phenotype. | Anderson and Smith found that at 44C germ-tube formation was completely inhibited in Aspergillus niger, although spherical growth could occur over a prolonged period to produce large spherical cells. More generally, there are more dimorphic fungi that display such a distinctive phenotypic transition at elevated temperatures. This made us ponder and let to the idea of generating a single cellular phenotype. | ||
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<h4>Rationale</h4> | <h4>Rationale</h4> | ||
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Figure 1) Schematic representation bioreactor | Figure 1) Schematic representation bioreactor | ||
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<h2>Strategy 1: Directed evolution</h2> | <h2>Strategy 1: Directed evolution</h2> | ||
Revision as of 18:24, 8 September 2013
- Safety introduction
- General safety
- Fungi-related safety
- Biosafety Regulation
- Safety Improvement Suggestions
- Safety of the Application
Engineering morphology
Host engineering
Generating single cell factories
Introduction
Synthetic biology doesn’t stop at the level of molecular systems. To expand the scope of this project we have chosen for a multi-level approach, in which we are working on biobricks, proteins, a pathway and also our host. In order to achieve the latter two strategies have been conceived of. In the first we have chosen to harness the power of directed evolution, a powerful tool that not often used in this competition. An explanation for this might lie in the fact that this approach is only semi-rational at best, however we like to argue that this does not make it any less of a powerful mechanism, and neither within the field of synthetic biology. Nonetheless, in order to explore new territories we have chosen for a second, fully rational approach in which we analyze the transcriptome of two distinct phenotypes; the mycelial and the single cell.
A scientific paper from 1971
Anderson and Smith found that at 44C germ-tube formation was completely inhibited in Aspergillus niger, although spherical growth could occur over a prolonged period to produce large spherical cells. More generally, there are more dimorphic fungi that display such a distinctive phenotypic transition at elevated temperatures. This made us ponder and let to the idea of generating a single cellular phenotype.
Rationale
The secretion capacity of Aspergillus niger is the feature mainly contributing to its status as excellent industrial workhorse. However, when we investigate this process in more detail, we find that only the hyphal tips of the mycelium are actively secreting. Since the vegetative mycelium poses a burden, generating single cells.From a process-oriented perspective the potential of host engineering is also interesting. A single cellular phenotype will result in a higher surface to volume ratio, thus effectively increasing the exchange area, while at the same time it annihilates pore clogging. A unicellular strain could be cultured in a similar fashion as a yeast, such as Saccharomyces cerevisiae . The fact that this research intersects with a fundamental topic, the evolution of multicellularity, makes it even more interesting. Figure 1) Schematic representation bioreactor
Strategy 1: Directed evolution
The power of experimental evolution with regard to complex adaptations has been demonstrated in recent research, allowing acquisition of multicellular Saccharomyces cerevisiae. The other way around one can envision evolution of a unicellular mutant of the filamentous fungus Aspergillus niger. Obtaining such a mutant could help greatly in identifying genes related to multicellularity in complex fungi, a field that is largely unexplored.
Aim
Obtain a single cell phenotypic Aspergillus niger strain by directed evolution
Strategy 2: Comparative transcriptomics
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