9:00-17:00: Make ESTM 5&6 inoculation plates as described before.
17:05-17:50: Make 10, 100, 1,000 and 10,000 dilution series for following inoculated solutions from ESTM 3 plates and plate and aliquot of each dilution onto a petri dish to observe bacteria growth: G3 (no bleached phenotype which is the phenotype in interest); D6 (bleached phenotype as positive control)
Day 16
9:00-10:00: Set up ML1 activation line 122~181.
10:00-12:00: WHMIS safety training session.
13:00-14:35: Make Col-0 seedling stocks in 96-well plates(18).
14:35-15:35: Make two ecotype seedling stocks.
15:40-18:25: Make ML1 activation line 122~181 media stocks.
Day 16
9:00-9:50: Wash 96-well plates.
9:50-10:30: Plate the bacteria from glycerol stocks ESTM 5&6 to new plates.
10:30-11:45: Transplant Col-0 from pot to tra with soil (2).
11:45-12:10: Wash and rinse 96-well plates.
13:00-13:40: Bacteria colony count for leaf tissue plate prepared on Friday.
13:40-15:00: Harvest seeds.
15:20-15:40: Recycle the beads in leaf tissue solutions in tubes using sieve.
15:40-16:25: Make seedling stocks (Col-0 with transposon inserted)in 96-well plates by adding 200 micro litre MS+MES media to each well and freeze for storage.
Day 15
Smex is light sensitive.
10:15-10:50: ESTM 1&2 inoculation line result recording.
10:50-11:55: Make 10, 100 and 1,000 dilution of selected ESTM line wells and to observe bacteria growth by taking an aliquot of each one (5 micro litres) onto a petri dish.
12:00-13:40: Make 10, 100, 1,000 and 10,000 dilutions of solution of leaf tissue syringed by bacteria Tuseday (#5-16). Take an aliquot (5 micro litres) of each dilution onto petri dish to record bacteria growth.
14:20-17:00: Make Col-0 stock in 96-well plates with 200 micro litre MS+MES media (28 plates).
17:00-17:45: Add diluted pathogen #524 solution to plates with ecotype 1&2.
Add diluted pathogen #500 solution to ML1 activation line in DMSO or Smex media prepared this morning.