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<thead> | <thead> | ||
<tr> | <tr> | ||
− | <th> | + | <th>Species (Strain)</th> |
− | <th> | + | <th>Colony Pigmentation</th> |
− | <th> | + | <th>Colony Morphology</th> |
+ | <th>Points of Interest</th> | ||
</tr> | </tr> | ||
</thead> | </thead> | ||
<tbody> | <tbody> | ||
<tr> | <tr> | ||
− | <td> | + | <td><i>Azorhizobium caulinodans</i> (ORS571)</td> |
− | <td> | + | <td>White</td> |
− | <td> | + | <td>Regular form, Typically raised, Entire margin</td> |
+ | <td>Colonies rarely grow to a measurable size when grown at 30˚c on YEB media after 24 hours</td> | ||
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td> | + | <td><i>Azospirillum brasilense</i> (SP245)</td> |
− | <td> | + | <td>Orange/Pink</td> |
− | <td> | + | <td>Non-slimy, Regular and round form, Entire margins</td> |
+ | <td>Both immature and dead colonies lack the orange/pink pigment, Colonies wrinkle with age</td> | ||
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td> | + | <td><i>Herbaspirillum seropedicae</i> (Z67)</td> |
− | <td> | + | <td>Cream/Light Green</td> |
− | <td> | + | <td>Circular or Irregular form (occasionally rhizoid), Raised elevation, Shiny</td> |
− | + | <td>Colonies took on a different morphology depending on how the media was innoculated; stab-innoculation lead to rhizoid form while spreading leads to circular/irregular form</td> | |
</tr> | </tr> | ||
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</table> | </table> | ||
− | <font size="2">Table 1: | + | <font size="2">Table 1: Qualitative analysis of <i>Azorhizobium caulinodans</i>, <i>Azospirillum brasilense</i>, <i>Herbaspirillum seropedicae</i> colonies grown on solid media.</font> |
</div> | </div> |
Revision as of 11:02, 12 October 2018
Alternative Roots
Characterising Bacterial Growth on Solid Media
Rationale
In order to understand chemotaxis on agar, it was important to understand how the selected bacteria (Azospirillum brasilense, Azorhizobium caulinodans and Herbaspirillum seropedicae) grow on solid media in standard laboratory conditions. This measure would serve as a control to which experimental plates would be compared to. Familiarisation of bacteria also allows identification of abnormal behaviour and contamination.
Experimental Approach
Each species was grown on 1% agar. The type of agar utilised was selected from DSMZ suggestions which states which media is appropriate for each species [1-3]. Overnight culture for each species were then spread on 3 individual agar plates which were labelled and incubated at the DSMZ suggested temperature for 24-48hours (depending on the species). More details about out experimental design can be found on the protocol page.