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. 2014 Aug 25;9(8):e105594. doi: 10.1371/journal.pone.0105594

Table 1. Enzymes used in the synthesis of DPM.

aEnzyme EC # Gene Source Substrate d K m (mM) d k cat (sec−1)
bACS 6.2.1.1 Acs1 S. cerevisiae Acetate CoA 0.28 0.24 10
cACT 2.3.1.9 mvaE E. faecalis Ac-CoA 0.60 2.3
cHMGS2 2.3.3.10 mvaS E. faecalis acac-CoA Ac-CoA 0.015 0.35 1.0
cThRed 1.1.1.34 mvaE E. faecalis HMG-CoA 0.023 0.55
cHMGR 1.1.1.34 mvaE E. faecalis HMG-CoA 0.020 0.67
cMVK 2.7.1.36 mvaK1 S. aureus Mev 0.027 19
cPMK 2.7.4.2 mvaK2 S. pneumoniae P-mev 0.0042 5.0
bPK 2.7.1.40 PKM2 O. cuniculus PEP 0.040 160
bMK 2.7.4.3 AK1 O. cuniculus AMP e0.50 e410
bPPiase 3.6.1.1 Ppa1 S. cerevisiae PPi e0.0050 e260
a

Abbreviations: ACS, acetyl-CoA synthetase; ACT, acetoacetyl-CoA thiolase; HMGS2, HMG-CoA synthase; ThRed, acetoacetyl-CoA thiolase/HMG-CoA reductase (dual-function enzyme); HMGR, HMG-CoA reductase; MVK, mevalonate kinase; PMK, phosphomevalonate kinase; PK, pyruvate kinase; MK, myokinase; PPiase, inorganic pyrophosphatase.

b

Obtained from commercial sources.

c

Expressed in E. coli and purified.

d

Standard errors are <5% in all cases (see Materials and Methods ).

e

Parameters taken from literature (MK [77], [78], PPiase [79], [80]).