A strain of Acinetobacter lct-h3
A LCT-H3, bacillus technology, applied in bacteria, microorganisms, microorganisms, etc., can solve the problem that genetic information is difficult to obtain
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Embodiment 1
[0023] Implementation example one: strain LCT-H3 culture.
[0024] The strain LCT-H3 is a descending strain isolated from the condensed water in the return cabin of the "Shenzhou 9" spacecraft. The strains were cultured statically or shaken in a 37°C incubator or shaker. The liquid medium was LB (Trptone 10g / L, Yeastextract 5g / L, NaCl 5g / L, pH7.3), and the solid medium was MH flat.
Embodiment 2
[0025] Implementation example two: strain LCT-H3 strain identification and phylogenetic tree construction.
[0026] LCT-H3 was inoculated into LB liquid medium, cultivated overnight at 37°C, 180rpm, centrifuged at 6000rpm for 5min to collect the bacteria, and discarded the supernatant. The genomic DNA of the collected bacteria was extracted using the Genomic DNA Extraction Kit (Code No. 51304, detailed steps refer to the product manual) of Qiagen Company. Using the genomic DNA of LCT-H3 as a template, the 16s rRNA fragment was amplified and sequenced using bacterial 16s rRNA universal sequencing primers 27F (5'-AGAGTTTGATCCTGGCTCAG-3') and 1492R (5'-TACGGCTACCTTGTTACGACTT-3') to obtain its bases sequence. Use CLUSTALW (http: / / www.ebi.ac.uk / Tools / msa / clustalw2 / ) for multiple sequence alignment, and use MEGA 5.0 to construct the NJ phylogenetic tree ( figure 1 ).
Embodiment 3
[0027] Implementation example three: Gram staining of bacterial strain LCT-H3.
[0028] The Gram staining kit (Code No. G1060, Solarbio) was used to perform Gram staining on the LCT-H3 cells. Cultivate the bacteria overnight in LB liquid medium, drop the bacteria solution on the center of the glass slide, and warm it slightly on the alcohol lamp to make it dry quickly. Crystal violet and sand yellow staining solution can be used to stain and decolorize the dried bacteria at one time. For detailed steps, please refer to the product manual. After the staining is completed and dried, put it under an optical microscope to observe the staining situation, first find the target field of view with a low-power microscope, and then observe with an oil lens (100×), judge and record the results, and take pictures, see figure 2 , Gram-negative bacilli in a single, scattered arrangement.
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