Apply in sillico medium to bakers yeast metabolic network model iND750 by Duarte et al. 2004.
ypd(model, def_bnd = SYBIL_SETTINGS("MAXIMUM"), ver = "harrison2007")An object of class modelorg.
A single numeric value. Absolute value for uppper and lower bounds for
reaction bounds.
Default: SYBIL_SETTINGS("MAXIMUM").
A single character string giving the version of the YPD medium. Can be set
to harrison2007 or bilu2006 (see Details below).
Default: harrison2007.
An instance of class modelorg with input fluxes set
corresponding to the desired YPD medium.
The function ypd identifies exchange reactions via the function
findExchReact. The lower bounds of all exchange fluxes is set
to zero (not allowing any flux into the network) and the upper bounds are set
to the value of def_bnd (default: output is unbounded). The lower bound
input of the input fluxes is set like in the table below.
Two different versions of YPD medium are available: Harrison et al. 2007 and Bilu et al. 2006.
Harrison et al 2007:
EX_ala_L(e) |
\(-0.5\) |
EX_arg_L(e) |
\(-0.5\) |
EX_asn_L(e) |
\(-0.5\) |
EX_asp_L(e) |
\(-0.5\) |
EX_chol(e) |
\(-0.5\) |
EX_cys_L(e) |
\(-0.5\) |
EX_dcyt(e) |
\(-0.5\) |
EX_ergst(e) |
\(-0.5\) |
EX_glc(e) |
\(-20\) |
EX_glu_L(e) |
\(-0.5\) |
EX_gly(e) |
\(-0.5\) |
EX_gua(e) |
\(-0.5\) |
EX_h(e) |
def_bnd * -1 |
EX_hdca(e) |
\(-0.5\) |
EX_his_L(e) |
\(-0.5\) |
EX_leu_L(e) |
\(-0.5\) |
EX_lys_L(e) |
\(-0.5\) |
EX_met_L(e) |
\(-0.5\) |
EX_nh4(e) |
def_bnd * -1 |
EX_o2(e) |
\(-2\) |
EX_ocdca(e) |
\(-0.5\) |
EX_pi(e) |
def_bnd * -1 |
EX_pro_L(e) |
\(-0.5\) |
EX_ser_L(e) |
\(-0.5\) |
EX_so4(e) |
def_bnd * -1 |
EX_thr_L(e) |
\(-0.5\) |
EX_thymd(e) |
\(-0.5\) |
EX_trp_L(e) |
\(-0.5\) |
EX_ttdca(e) |
\(-0.5\) |
EX_tyr_L(e) |
\(-0.5\) |
EX_ura(e) |
\(-0.5\) |
Bilu et al 2006:
EX_nh4(e) |
def_bnd * -1 |
EX_pi(e) |
def_bnd * -1 |
EX_so4(e) |
def_bnd * -1 |
EX_glc(e) |
\(-20\) |
EX_o2(e) |
\(-2\) |
EX_ala_L(e) |
\(-0.5\) |
EX_arg_L(e) |
\(-0.5\) |
EX_asn_L(e) |
\(-0.5\) |
EX_asp_L(e) |
\(-0.5\) |
EX_cys_L(e) |
\(-0.5\) |
EX_his_L(e) |
\(-0.5\) |
EX_leu_L(e) |
\(-0.5\) |
EX_lys_L(e) |
\(-0.5\) |
EX_met_L(e) |
\(-0.5\) |
EX_pro_L(e) |
\(-0.5\) |
EX_ser_L(e) |
\(-0.5\) |
EX_thr_L(e) |
\(-0.5\) |
EX_trp_L(e) |
\(-0.5\) |
EX_tyr_L(e) |
\(-0.5\) |
EX_dcyt(e) |
\(-0.5\) |
EX_gly(e) |
\(-0.5\) |
EX_gua(e) |
\(-0.5\) |
EX_thymd(e) |
\(-0.5\) |
EX_h2o(e) |
def_bnd * -1 |
EX_na1(e) |
def_bnd * -1 |
EX_k(e) |
def_bnd * -1 |
EX_co2(e) |
def_bnd * -1 |
EX_ade(e) |
\(-0.5\) |
EX_gln_L(e) |
\(-0.5\) |
EX_ile_L(e) |
\(-0.5\) |
EX_phe_L(e) |
\(-0.5\) |
EX_val_L(e) |
\(-0.5\) |
Harrison, R., Papp, B., Pal, C., Oliver, S. G. and Delnert, D. (2007) Plasticity of genetic interactions in metabolic networks of yeast. PNAS 104, 2307--2312.
Bilu, Y., Shlomi, T., Barkai, N. and Ruppin, E. (2006) Conservation of expression and sequence of metabolic genes is reflected by activity across metabolic states. PLoS Comput Biol 2, 932--938.
'>modelorg, findExchReact and
SYBIL_SETTINGS