From 217de5857f651bf3ba3534007b3f1c7f504907dd Mon Sep 17 00:00:00 2001 From: Aadityanshu Abhinav <aaadityanshu@gmail.com> Date: Wed, 2 Oct 2024 12:56:01 +0000 Subject: [PATCH] Update file notebook.html --- wiki/pages/notebook.html | 2 +- 1 file changed, 1 insertion(+), 1 deletion(-) diff --git a/wiki/pages/notebook.html b/wiki/pages/notebook.html index 1d5e1c8..27bb46b 100644 --- a/wiki/pages/notebook.html +++ b/wiki/pages/notebook.html @@ -335,7 +335,7 @@ <h3 style="text-align:justify"><b>Bacteria</b></h3> <ul style="text-align:justify"> <li>We found a protocol which used a defined differential media - NBRISSM. We decided to swap the magnesium trisilicate suggested by the media with calcium aluminosilicate to suit the requirements of our studies.</li> - <li>n order to make NBRISSM media as per the protocol, we prepared hydroxyapatite in our lab after consulting with experts from the Materials Science Lab at IIT Madras.</li> + <li>In order to make NBRISSM media as per the protocol, we prepared hydroxyapatite in our lab after consulting with experts from the Materials Science Lab at IIT Madras.</li> <li>We inoculated <em>P. fluorescens</em> in our modified NBRISSM media with different BCP (indicator) concentrations and placed it in a shaking incubator at 30°C and observed every 24 hours for any color change.</li> <li>We established an experimental protocol for inoculating <em>P. fluorescens</em> in the Martian soil simulant after consulting Prof. K Chandraraj, a soil microbiology expert at IIT Madras. We created a cell suspension of <em>P. fluorescens</em> in fresh LB and poured in martian soil simulant. The flask with inoculated soil was kept in a shaking incubator at 30°C. 1 gm of this soil was used the next day to count CFU. We noticed contamination while observing CFU.</li> -- GitLab