Chemistry & Biology 16

Supplemental Data

Adenylation Enzyme Characterization

Using γ -18O4-ATP Pyrophosphate Exchange

Vanessa V. Phelan, Yu Du, John A. McLean, and Brian O. Bachmann

Chemicals and general methods LR-recombination using Gateway LR Clonase enzyme

mix (Invitrogen). The resulting plasmid was introduced
All chemicals were obtained from Sigma-Aldrich unless into the ROSETTA E. coli strain (Novagen). The culture
otherwise noted. γ−18O4-ATP was obtained from was inoculated (1:100) with an overnight culture made
Cambridge Isotope Labs (Cambridge, MA). 4-methyl-3- from a fresh colony of the above strain and grown at
hydroxyanthranilic acid was prepared by catalytic 37°C in a 2.8 L baffled flask containing 500 mL LB
hydrogenation of 4-methyl-3-hydroxy-2-nitrobenzoic acid medium with 100 µg/mL ampicillin until OD600 = ~ 0.6.
with Pd/C and H2 at 1 atm in ethanol (Keller et al., 1984). IPTG was then added (final concentration of 0.5 mM)
Protein concentrations were measured with Pierce® and the culture grown overnight at 25°C. The 63 kD His-
BCA Protein Assay Kit (Thermo Scientific). tagged protein was purified as described above.

Cloning, Expression and Purification of A-domains

TycA PheATE. Overproduction of the 110kD His-tagged

TycA PheATE was performed in E. coli BL21(DE3) 75 kDa
bearing the vector pSU18-tycAPheATE-His (Gruenewald
et al., 2004). In a 2.8-L baffled flask, 500 mL LB 50 kDa
medium containing 30 µg/mL chloramphenicol was
inoculated (1:100) with an overnight culture made from a
fresh colony of the above strain and grown at 37 °C in a
2.8 L baffled flask until OD600 ~ 0.6. IPTG was then
added to yeild a final concentration of 0.5 mM and the
culture was incubated for an additional 20 h at 30 °C.
The cells were pelleted (30 min, 3750 rpm, 4 °C) and
resuspended in binding buffer (500 mM NaCl, 20 mM
NaH2PO4, 20 mM imidazole, pH 7.4). For cell lysis,
DNase I (NEB, 0.2 U/mL) was added, the cells were Figure S1. Overproduction of ORF21. From left to right,
disrupted using a French Press and filtered through a Lane 1: Molecular weight markers; Lane 2: Uninduced
0.45-µm filter. The protein was purified on a HisTrap FF cell free extract; Lane 3: Induced cell-free extract; Lane
column (GE Healthcare) on an ÄKTA chromatography 4: Flow through of from Ni2+ affinity column; Lane 5:
system (GE Healthcare) using binding buffer with Pooled fractions from Ni2+ affinity column; Lane 7:
linearly increasing imidazole concentration (20–500 Desalted ORF21.
mM). The enriched target protein fraction was then
desalted with a HiTrap Desalting column using 20 mM
Tris, pH 7.5 and stored in aliquots at –80°C in storage Kinetic Parameters for TycA. For TycA kinetic
buffer containing 5% glycerol and 1 mM DTT. measurements, the reactions were performed as
described with the following modifications: % exchange
Val-A. Production of the 56.6 kDa his-tagged Val-A was was measured over a range of L-Phe concentrations
performed in E. coli BL21(DE3) bearing the vector pBS3 (0.118 – 0.15 mM) and rates were measured in triplicate
(Du and Shen, 1999)]. The conditions for expression and as single time points at 3 minutes. In all cases the %
purification are similar to those described above except exchange of reactions did not exceed 12%. The
50 µg/ml kanamycin was added to the medium instead ‘apparent’ substrate dependence parameters, KM and
of chloramphenicol. kcat, were calculated from initial velocity time curves with
varied L-Phe concentrations using a non-linear least
ORF21. ORF21 was cloned from the Streptomyces square fit to the Michaelis-Menten equation using Prism
refuineus genomic DNA via PCR using the primers (GraphPad software).
5’-CACCATGACAGTACGCAGCACCGCC-3’ and
5’-GCCTCGGGAACGCTTGGTG-3’ (synthesized by Kinetic Parameters for Orf21. For Orf21 kinetic
Sigma-Aldrich). The 1.8 kb PCR product was cloned into measurements, the reactions were performed as
the vector pENTRTM/SD/D-TOPO® using the pENTR™ described with the following modifications: % exchange
directional TOPO cloning kit (Invitrogen). The gene was was measured over a range of MHA concentrations
subcloned into an expression vector pET-DEST42 via (11.5 – 50.0 µM) and HA concentrations (0.115 – 0.500
mM) and rates were measured in triplicate as single time
points at 10 minutes or 15 minutes in order to assure
that the maximal % exchange of reactions was
maintained below 15%. The ‘apparent’ substrate
dependence parameters, KM and kcat, were calculated as
described above from initial velocity time curves with
varied MHA or HA concentrations.

Mass Spectrometry

MALDI-TOFMS. MALDI-TOFMS analyses were

performed on a Voyager-DE™ STR (Applied ESI-LC/MS
Biosystems, Inc.) using a nitrogen laser (337 nm). Prior
to analysis, 1µL of analyte/matrix mixture was spotted on
to a stainless steel MALDI target. External mass
calibration was performed in the reflectron mode using a
mixture of γ−18O4-ATP and γ−16O4-ATP. Mass spectra
were acquired in the negative ion mode over a range of
450 to 1200 m/z. Mass spectra for ATP-PPi exchange
analysis were obtained by averaging 100 consecutive
laser shots. Data acquisition and quantitative spectral
analysis was conducted using Applied Biosystems
DataExplorer software, version 4.5.
ESI-LC/MS/MS
ESI-LC/MS analyses were performed on a
ThermoFinnigan LTQ linear ion trap mass spectrometer
(Thermo Fisher Scientific, Waltham, MA) equipped with
an ESI interface in negative ion mode. Nitrogen was
used both for the auxiliary and sheath gas. The auxiliary
and sheath gases were set to 20 psi and 36 psi,
respectively. The following instrumental parameters
were used: capillary temperature 300 °C; source voltage
4.5 kV; source current 100 µA capillary voltage -49.0 V;
tube lens -148.30 V; skimmer offset 0.00 V; activation
time 50 ms with an isolation width of 1 m/z. The
sensitivity of the mass spectrometer was tuned by
infusion of γ-16O4-ATP at a flowrate of 0.1 mL/min. Figure S2. Limit of turnover detection for MALDI-
Samples were introduced by a Waters Acquity UPLC TOFMS, ESI-LC/MS and ESI-LC/MS/MS detection
system (Waters, Milford, MA) with an injection volume of methods. “% γ-16O4-ATP” is the mass spectometric
5µL. γ−18O4-ATP was separated from contaminating measured ratio of 16O/(18O+ 16O). Top: MALDI-TOFMS
salts on a 5µm Hypercarb column (3 x 50mm, detection (in triplicate) of γ-16O4-ATP in 1mM γ-18O4-ATP
ThermoFisher Scientific) with an isocratic method of in reaction mixture demonstrated reliable detection
82.5% 20 mM ammonium acetate pH 6 containing 0.1% above 1 % exchange (10 µM). Middle: Similar
diethylamine and 17.5% acetonitrile over 5 minutes with measurement using ESI-LC/MS detection permitted
a flow rate of 0.2 mL/min. A divert valve was employed detection levels above 0.1% exchange (1 µM). Bottom:
for the first two minutes of the chromatographic run in Similar measurement using ESI-LC/MS/MS detection
order to avoid introducing salts into the source. The permitted detection levels above 0.01% exchange (100
retention time of ATP species under these conditions nM). MALDI-TOFMS is more rapid (<30 sec.) as
was approximately 3 minutes. reaction mixtures are analyzed without the Hypercarb
sample cleanup.
Selected Reaction Monitoring. For ESI-LC/MS/MS
studies, the selection reaction monitoring mode was
used with a collision energy of 20eV. The mass
transitions of (506 Æ 408), (508 Æ 408. 410), (510 Æ
408, 410, 412), (510 Æ 408, 410, 414) and (514 Æ 408,
410, 412, 414, 416) corresponding to unlabeled, partially
labeled and fully labeled ATP were monitored. Data
acquisition and quantitative spectral analysis was
conducted using the Thermo-Finnigan Xcaliber software,
version 2.0 Sur 1. Time course study of γ−18O4-ATP stability under
assay conditions
Limits of detection figures

Limits of detection (LOD) experiments were performed

by spiking TycA assay reactions containing no amino
acid with known concentrations of γ−16O4-ATP ranging
from 0 to 0.1mM. These conditions accurately simulate
the exchange reaction.

MALDI-TOFMS
Figure S3. 18O ATP lability in 15 hour time course with
no TycA (‹), no substrate („), glutamate (S) and
phenylalanine (z). Over 15 hours γ-18O4-ATP is stable
when no enzyme is present. γ-18O4-ATP only becomes
significantly depleted after two hours when γ-18O4-ATP is
incubated with TycA without amino acid or with incorrect
amino acid present. However, γ-16O4-ATP created by
loss of all four 18O labels is still only 25% while exchange
of 1, 2 or 3 18O labels accounts for the decrease of γ-
18
O4-ATP detected. The loss of 18O labels can be
corrected for by calculating the ratio of the area of γ-
16
O4-ATP to the area of total ATP and subtracting the
substrate free control.

Enhanced sensitivity MALDI assay

Figure S4. Enhanced sensitivity of MALDI-TOFMS

detection of TycA substrate activation by γ−18O4-ATP-PPi
exchange. Activities were monitored via MALDI-TOFMS
by incubating 1µM TycA for two hours in reaction
mixture containing 1mM γ-18O4-ATP, 1mM amino acid,
5mM MgCl2 and 5mM pyrophosphate in 20mM Tris pH
7.5.

SUPPLEMENTAL REFERENCES

Du, L.C., and Shen, B. (1999). Identification and

characterization of a type II peptidyl carrier protein from the
bleomycin producer Streptomyces verticillus ATCC 15003.
Chemistry & Biology 6, 507-517.
Gruenewald, S., Mootz, H.D., Stehmeier, P., and
Stachelhaus, T. (2004). In vivo production of artificial
nonribosomal peptide products in the heterologous host
Escherichia coli. Applied and environmental microbiology
70, 3282-3291.
Keller, U., Kleinkauf, H., and Zocher, R. (1984). 4-Methyl-3-
hydroxyanthranilic acid activating enzyme from actinomycin-
producing Streptomyces chrysomallus. Biochemistry 23,
1479-1484.