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Expand Up @@ -288,6 +288,39 @@ ecological_interactions:
evidence_source: IN_VITRO
snippet: exchange of further molecules beyond the unidirectional feeding with sucrose
explanation: Supports additional interaction mechanisms beyond the engineered sucrose cross-feeding link.
cultivation_setup:
- cultivation_mode: BATCH
system_type: FLASK
working_volume: 10.0
working_volume_unit: mL
instrument_detail: >-
125 mL baffled Erlenmeyer flasks holding roughly 10 mL of alginate-bead suspension in M3
minimal medium, on a Multitron Pro rotary shaker. The cyanobacterium is encapsulated in
barium-alginate hydrogel rather than free in suspension; that encapsulation is what
shields it from 2,4-DNT toxicity, so it is a property of the setup and not of the strain.
Cells were stepped from 25 to 50 mM NaCl over two days before the final medium.
notes: >-
No operating temperature or light intensity. The paper gives 32 °C and 150 rpm for
Lysogeny broth cultures, and LB is the P. putida preculture medium - the coculture runs
on M3 with light and CO2 as inputs, so those numbers are not the community's (#529). The
incubator model is recorded instead of a temperature invented for it.

`cultivation_mode` is BATCH: the medium is exchanged between acclimation steps rather
than fed continuously, and no dilution rate is reported.
evidence:
- reference: PMID:32064751
supports: SUPPORT
evidence_source: IN_VITRO
snippet: the alginate bead suspension were portioned in ~ 10‐ml aliquots into 125‐ml baffled
Erlenmeyer flasks
explanation: The vessel and the working volume the coculture was run in.
- reference: PMID:32064751
supports: SUPPORT
evidence_source: IN_VITRO
snippet: By encapsulating S. elongatus within a barium-alginate hydrogel, cyanobacterial cells
were protected from the toxic effects of 2,4-DNT, enhancing the performance of the co-culture
explanation: Why the encapsulation belongs in the setup rather than being incidental.

environmental_factors:
- name: Light and CO2
value: Illumination with CO2 as primary carbon input
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