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.
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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.

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  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

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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
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         EPA
   PERMIT No. G-35
Official Business
Penalty for Private Use $300

EPA/600/S2-90/034

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