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Chapter-5<br />

Synthesis of highly substituted pyrroles<br />

Procedure<br />

1. Inoculate test organism on the top of Mueller Hinton Agar plate with help of<br />

sterile swab. (it can be inoculated in melted agar also )<br />

2. The swab was dipped in the inoculum and surface of plate was streaked with<br />

swab.<br />

3. Streaking was repeated for 3 times and each time the plate was rotated at angle<br />

of 60º.<br />

4. Sterilize the cup-borer make four cups of the diameter of 8-10 mm. at equal<br />

distance in the plate previously inoculated with seed culture.<br />

5. The depth of well was 2.5-5.0 mm.<br />

6. The wells have been clearly punched so the surrounding medium is not lifted<br />

when the plug was removed out.<br />

7. The plates were incubated at 37ºC for 24 h. Then the zone of inhibition<br />

measured and the size of zone cited in table.<br />

Department of Chemistry, <strong>Saurashtra</strong> <strong>University</strong>, Rajkot-360005 174

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