Glycerol → L-Lysine

HRID 1873328Notes

Reaction equation

HRID 1873328 reaction equation
C1[C:6]([CH2:7][CH2:8][NH2:9])=[CH:5]C=C(S(F)(=O)=O)C=1.[OH:14]CC(CO)O.C1[N:25]([CH2:26][CH2:27][OH:28])CCN(CCS(O)(=O)=O)C1>>[NH2:25][C@H:26]([C:27]([OH:28])=[O:14])[CH2:5][CH2:6][CH2:7][CH2:8][NH2:9]

Participants

4

Procedure

smegmatis or M. bovis BCG cultures with an optical density measured at 600 nm (OD600) of 0.5 were centrifuged at 10000 g for 15 min. The pellet was re-suspended in 10 ml of 50 mM Hepes buffer (pH 7.4) containing 1 mM of AEBSF (Pefabloc Sc, Roche) and 15% (v/v) of glycerol (buffer A). The cells then underwent continuous sonication for 10 minutes at 4° C. using a Branson type sonicator, the outlet power being adjusted to 5. The total cell lysate was centrifuged at 4° C. at 20000 g for 15 min. For the methylation tests, 300 μl of total clarified lysate containing 1 mg of protein per ml was mixed with 40 μl of [methyl-14C]AdoMet (60 mCi/mmol, Amersham Pharmacia Biotech), 100 μl of recombinant HBHA purified on a heparin column to 0.5 mg/ml, 5 μl of 1M MgCl2 and 55 μl of buffer A. The methylation tests were carried out at 25° C. 100 μl samples were removed at intervals to verify the degree of methylation of the recombinant HBHA by autoradiography.

Workup

  1. customThe cells then underwent continuous sonication for 10 minutes at 4° C.
  2. waitThe total cell lysate was centrifuged at 4° C. at 20000 g for 15 min
  3. additioncontaining 1 mg of protein per ml
  4. custompurified on a heparin column to 0.5 mg/ml, 5 μl of 1M MgCl2 and 55 μl of buffer A
  5. customwere carried out at 25° C
  6. custom100 μl samples were removed at intervals

Sources & evidence

ORD record
ord-b4876f6a4cf9481288218a14ee9927d0
Source dataset
uspto-grants-2012_11
Patent number
US08303963B2

Reaction notes

Loading…