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#Question id: 10503


A Pseudomonas species that synthesizes the antifungal compound against the pathogenic fungus Gaeumannomyces graminis known as

#I Life Science/ Life Sciences Group – I-V
  1. N-(17-hydroxylinolenoyl)-l-glutamine
  2. 12-oxo-phytodienoic acid (OPDA)
  3.  JAZ–COI1 complex
  4. 2,4-diacetylphloroglucinol 

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TLS Online TPP Program

#Question id: 5528

#SCPH06 I Botany

The lining of the uterus in which the mammalian embryo implantationsTakes place called as

TLS Online TPP Program

#Question id: 15589

#SCPH05 I Biotechnology

Reynold’s number is ratio of:

TLS Online TPP Program

#Question id: 65

#SCPH05 I Biotechnology

Identify which of the following pair is enantiomers, diastereomers or meso compounds.

TLS Online TPP Program

#Question id: 13089

#SCPH28 | Zoology

To express a yeast gene in E. coli, your task is to design a strategy to insert the yeast gene into the bacterial plasmid. Below is a map of the area of the yeast genome surrounding the gene in which you are interested.

 
The distance between each tick mark placed on the line above is 100 bases in length
Below are the enzymes you can use, with their specific cut sites shown 5’-XXXXXX-3’ 3’-XXXXXX-5’

 
The plasmid is 5,000 bases long and the two farthest restriction enzyme sites are 200 bases apart. The plasmid has an ampicillin resistance gene somewhere on the plasmid distal from the restriction cut sites.
                              
You do the digestion of the insert and the vector and then ligate the two digestions together. You then transform the ligation into bacteria and select for ampicillin resistance. You get three colonies on your transformation plate. You isolate plasmid from each one and cut each plasmid with the enzyme XbaI. You then run your three digestions on an agarose gel and see the following patterns of bands. Describe what each plasmid actually was that was contained in each of the three colonies.
 
What is the Colony 2’s plasmid is;

TLS Online TPP Program

#Question id: 15238

#SCPH06 I Botany

Electrophoretic resolution can be mainly changed by adjusting the
a) current 
b) pH of buffer system
c) luminous intensity 
d) Gel concentration