United States
Environmental Protection
Agency
Risk Reduction Engineering
Laboratory
Cincinnati OH 45268
Research and Development
EPA/600/S2-90/034 Dec. 1990
&EPA Project Summary
Biological Degradation of
Cyanide by Nitrogen-Fixing
Cyanobacteria
C. J. Gantzer and W. J. Maier
This study examined the ability of
nitrogen-fixing Anabaena to
biodegrade cyanide in batch
reactors. Mixed second-order rate
constants were obtained that
described the biologically mediated
decrease in cyanide for reactors
containing initial cyanide concentra-
tions of 3 ppm. For Anabaena
cultures not previously exposed to
cyanide, the rate constants were a
function of pH. Faster rates of
cyanide biodegradation were
observed at higher pH values.
Anabaena cultures acclimated to the
presence of cyanide had rate
constants that were at least 20 times
faster than rate constants for
unacclimated cultures.
Mixed second-order rate constants
were also obtained for the ability of
nitrogenase, the enzyme normally
responsible for nitrogen-fixation, to
reduce hydrogen cyanide to methane
and ammonia. Based on literature
values for nitrogen fixation, the rate
constants for methane production
were at least 10 times faster than
expected in batch reactors with initial
cyanide concentrations of 30 ppb.
This suggests that nitrogenase will
preferentially use hydrogen cyanide
rather than molecular nitrogen as a
substrate. Also, the rate constants for
methane production were of the
same order of magnitude as the rate
constants for total cyanide removal.
This indicates nitrogenase is an
important mechanism for the
biodegradation of trace concentra-
tions of cyanide.
The magnitude of the cyanide
biodegradation rate constants
suggests that the utilization of
nitrogen-fixing cyanobacteria in the
treatment of cyanide wastes can be a
feasible process in some applica-
tions, i.e., secondary or tertiary
treatment at larger treatment
facilities.
This Project Summary was
developed by EPA's Risk Reduction
Engineering Laboratory, Cincinnati,
OH, to announce key findings of the
research project that is fully
documented in a separate report of
the same title (see Project Report
ordering information at back).
Introduction
The basic premise of the study
summarized here was that the use of
nitrogen-fixing cyanobacteria (blue-green
algae) in the biological treatment of small
concentrations of free cyanides (HCN
and CN") can be a cost-effective
alternative to existing treatment
processes. A potential application of a
cyanobacteria-based process would be in
secondary treatment of cyanides that
escape alkaline chlorination. The steady
and small concentrations of cyanide in
the effluent of an alkaline-chlorination
process would be conducive to
maintaining cyanobacteria in a secondary
treatment process, i.e., alkaline chlori-
nation would protect the cyanobacteria
from cyanide concentration fluctuations.
Printed on Recycled Paper
-------
Because the extent of cyanide oxidation
in alkaline chlorination is an equilibrium-
driven phenomena, use of a microbial
process to detoxify the last fraction of
cyanide should result in lower alkaline-
chlorination operating costs.
Several potential advantages are
associated with the use of nitrogen-fixing
cyanobacteria in the biological treatment
of small concentrations of cyanide. First,
because cyanobacteria are photo-
synthetic, they do not require aeration to
obtain oxygen and do not require the
presence of organic substrates to
maintain biomass. Thus, the use of
cyanobacteria in the biological treatment
of small amounts of cyanide should have
lower operating costs than the use of
heterotrophic bacteria. Second, because
oJ the presence of cyanide-resistant
respiration and cyanide detoxification
pathways, nitrogen-fixing cyanobacteria
have the ability to survive in low to
moderate concentrations of hydrogen
cyanide. Third, the nitrogen-fixing
cyanobacteria can destroy hydrogen
cyanide with the enzyme nitrogenase.
Although normally responsible for
reducing molecular nitrogen (dinitrogen)
to ammonia, nitrogenase can also reduce
hydrogen cyanide to methane and
ammonia instead of its normal substrate
dinitrogen.
Despite the considerable amount of
information indicating the ability of
cyanobacteria to survive in the presence
of cyanide and to detoxify cyanide, the
kinetic data required to assess the
feasibility of using cyanobacteria in the
treatment of cyanide wastes does not
exist. This study provides an initial
assessment of the rate at which nitrogen-
fixing cyanobacteria are able to degrade
free cyanide.
Procedure
The objectives of the study were (1) to
determine the rates at which nitrogen-
fixing Anabaena cultures decreased total
cyanide concentrations and (2) to
determine the rate at which HCN was
reduced to methane by nitrogenase
activity. Rates of total cyanide
biodegradation were determined in a 1.3-
L reactor under batch conditions with
initial cyanide concentrations of 3,000 ug
CN/L. The extent of cyanide volatilization
was measured for each batch test, so that
the reported rate constants represented
biodegradation and not the sum of
biodegradation and volatilization. The
methane production experiments were
conducted in small 0.037-L, gas-tight
vials under batch conditions with initial
cyanide concentrations of 30 to 400 ug
CN/L.
Results and Discussion
Total Cyanide Biodegradation
Rates
The rate of cyanide biodegradation was
assumed to follow mixed second-order
kinetics,
— = -K,xs
dt b
irt, which.. S is the,, total -cyanide
concentration (ug CN/L), t is time (hr), Kb
is the mixed second-order rate constant
(L/[ug chl hr]), and X is the concentration
of Anabaena biomass in terms of
chlorophyll-a (ug chl/L).
For Anabaena cultures not previously
exposed to cyanide, the values of Kb
ranged from 5.0-10-6 to 2.2-10-4 L/(ug
chl/hr). This observed 44-fold variation in
Kb appeared to be a function of pH. That
is, as the time-averaged pH value for
each batch test increased, the observed
Kb value increased.
Because Kb increased as pH
increased, the Kb values were probably
responding to ALPHA,
ALPHA :
[HCN]
[HCN] + [CN ]
the fraction of the total free cyanide
existing as HCN. As pH values increase
to levels above the pKa (acid dissociation
constant) for HCN, the ALPHA values
decrease. Thus, the rate at which
unacclimated Anabaena cultures
decreased total cyanide concentrations
was optimized by reducing the fraction of
cyanide that HCN is more toxic and
inhibitory than is CN -.
One set of experiments was performed
to assess the effect that previous
exposures to cyanide had on
biodegradation rates. For batch tests
conducted at the same pH, an Anabaena
culture previously exposed to cyanide
had a mixed second-order rate constant
(Kb) 12 times greater than the Kb value
for a culture not previously exposed to
cyanide. Thus, when Anabaena had time
for enzyme induction, the rate constants
for cyanide biodegradation increased.
Methane Production Rates
The rate of methane production due to
nitrogenase activity was assumed to
follow mixed second-order kinetics,
— = K xs
dt n
in which P is the water-phase
concentration of cyanide corresponding
to the mass of methane produced (ug
CN/L), t is time (hr), Kn is the mixed
second-order rate constant for methane
production by nitrogenase (L/ug chl/hr]),
X is the concentration of Anabaena (ug
chl/hr), and S is the total cyanide
concentration (ug CN/L). Because
nitrogenase was not the only biological
mechanism" responsible for reducing
cyanide concentrations (S), in the vials,
determination of Kn involved fitting the
following equation to the methane
production data:
in which S0 is the cyanide concentration
at the start of the batch experiment (ug
CN/L) and Kb is the mixed second-order
rate constant for total cyanide
biodegradation by Anabaena cultures
(L/[ug chl/hr]), as determined in the
previous batch experiments.
The values of Kn obtained from the
batch experiments appeared to be an
inverse function of initial cyanide
concentrations. For example, for S0
values of 30 and 400 ug CN/L, the
observed Kn values were 2.6-10-4 and
2.6-10-6 L/(ug chl/hr), respectively. The
decrease in Kn with increasing S0 was
probably due to HCN inhibition of the
ATP (a form of biochemical energy)
generating pathways in the heterocysts.
The observed Kn value when S0 was
30 ug CN/L was almost 30 times larger
than a mixed second-order rate constant
for hydrogen cyanide reduction by
nitrogenase obtained from combining
existing in vivo nitrogen fixation data and
in vitro hydrogen cyanide reduction data.
This suggests that nitrogen-fixing
Anabaena cultures convert cyanide to
methane at a faster-than-expected rate.
Thus, if nitrogenase's requirements for
ATP and electrons can be continuously
satisfied, the enzymatic apparatus in
Anabaena normally responsible for
nitrogen fixing may play an important role
in determining the rate at which low
concentrations of cyanide are
biodegraded in a treatment process.
-------
Based on methane production data,
unacclimated Anabaena cultures have the
capacity to decrease total cyanide
concentrations from 30 ug CN/L to less
than 20 ug CN/L in 1.75 hr. The ability of
nitrogen-fixing cyanobacteria to reduce
cyanide concentrations below 20 ug
CN/L may be significant, because the
literature reports that no cyanide
destruction process has demonstrated
the ability to reduce total cyanide
concentrations to levels less than 25 ug
CN/L. Thus, nitrogen-fixing cyanobacteria
may be well suited for use in the
secondary or tertiary treatment of
cyanide wastes.
Conclusion and
Recommendations
In batch reactors with initial cyanide
concentrations of 3 mg CN/L, the mixed
second-order rate constants (Kb) for the
removal of cyanide by unacclimated
Anabaena cultures were a function of pH.
Faster rate constants were observed at
higher pH values. Because HCN is much
more toxic and inhibitory than CN~ and
because an increase in pH would reduce
HCN concentrations, the faster
biodegradation rates observed at higher
pH values were probably due to a
reduction in inhibition.
When previously exposed to cyanide,
Anabaena biodegraded cyanide at a
faster rate. The Kb value for an
acclimated Anabaena culture was 10
times faster than that for an unacclimated
Anabaena culture. Thus, reactors
operating under steady-state conditions
should have more rapid cyanide removal
rates than those observed in the batch
experiments.
In batch experiments with initial
cyanide concentrations of 30 ug CN/L,
the mixed second-order rate constant
(Kn) for the reduction of hydrogen
cyanide to methane by nitrogenase was
at least 10 times faster than expected
based on existing nitrogen-fixation kinetic
data. This supported the in vitro
observation that nitrogenase will
preferentially reduce hydrogen cyanide
rather than its normal substrate of
molecular nitrogen. Based on the amount
of methane produced during the batch
tests, nitrogenase activity decreased
cyanide concentrations from 30 to 20 ug
CN/L. Because few cyanide destruction
processes are able to attack cyanide at
such low concentrations, the use of
nitrogen-fixing cyanobacteria to treat
trace levels of cyanide is worth further
examination.
This study demonstrated the ability of
nitrogen-fixing cyanobacteria to
biodegrade small concentrations of free
cyanides in batch reactors. Future
studies need to examine the ability of the
cyanobacteria to degrade cyanide under
steady-state reactors to slight
perturbations in influent cyanide
concentrations. If such laboratory-scale
experiments continue to demonstrate the
attractiveness of using nitrogen-fixing
cyanobacteria to treat small and trace
cyanide concentrations, then a pilot-scale
study should be done to determine the
economic and technical feasibility of the
process.
This study was conducted through the
Minnesota Technical Assistance Program
(MnTAP) and the Minnesota Waste
Management Board. The full report was
submitted in partial fulfillment of
Cooperative Agreement CR 813437-01
under the sponsorship of the U.S.
Environmental Protection Agency.
U. S. GOVERNMENT PRINTING OFFICE: 1991/548-028/20157
-------
C. J. Gantzer and W. J. Maier are with the University of Minnesota, Minneapolis,
MN 55455.
James S. Bridges is the EPA Project Officer (see below).
The complete report, entitled "Biological Degradation of Cyanide by Nitrogen-
Fixing Cyanobacteria," (Order No. PB89-222 509/AS; Cost: $17.00, subject to
change) will be available only from:
National Technical Information Service
5285 Port Royal Road
Springfield, VA 22161
Telephone: 703-487-4650
The EPA Project Officer can be contacted at:
Risk Reduction Engineering Laboratory
U.S. Environmental Protection Agency
Cincinnati, OH 45268
United States
Environmental Protection
Agency
Center for Environmental Research
Information
Cincinnati OH 45268
BULK RATE
POSTAGE & FEES PAID
EPA
PERMIT No. G-35
Official Business
Penalty for Private Use $300
EPA/600/S2-90/034
------- |