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Applied and Environmental Microbiology, September 2001, p. 4349-4352, Vol. 67, No. 9
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.9.4349-4352.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Biosorption of Copper by a Bacterial Biofilm on a
Flexible Polyvinyl Chloride Conduit
Fouad M.
Qureshi,
Uzma
Badar, and
Nuzhat
Ahmed*
Centre for Molecular Genetics, University of
Karachi, Karachi 75270, Pakistan
Received 20 February 2001/Accepted 5 June 2001
 |
ABSTRACT |
Inexpensive technologies with less-than-optimal efficiencies as a
strategy for countering economic restraints to pollution control have
been evaluated by using a laboratory-scale biotreatment process for
copper-containing effluent. Economizing measures include the use of
polyvinyl chloride (PVC) cylinders fashioned from commercially available flexible PVC conduit to support a biofilm that was cultured in an inexpensive medium prepared in wastewater. The biofilm was challenged by aqueous copper solution in a bioreactor and subsequently analyzed under a scanning electron microscope with
energy-dispersive X-ray microanalysis.
 |
TEXT |
Removal of metals from industrial
wastewater has conventionally been accomplished mainly by
precipitation, ion exchange, and electrolytic technologies
(2). More recently, biosorption of metals by immobilized
cell systems has been used effectively for removal of metals from
industrial effluent (7). This technology exploits the
natural tendency of cells to accumulate elements or their innate
ability to degrade recalcitrant organic compounds. Cells with such
abilities are immobilized either as entrapped biomass or as a biofilm
to form a system for treating wastewater known as a bioreactor.
Entrapment techniques make use of various porous gels, resins, or
polymers to physically entrap (or rather embed) cells, whereas biofilms
are produced by coating a support surface with a thin film of cells.
Traditionally a very diverse range of materials
such as rocks, sands,
plastics, latex, paper, and steel, etc.
have been used as biofilm
supports. Polystyrene sheets, needle-punched polyester, and polyvinyl
chloride (PVC) foils in various geometries have lately been in use with
growing popularity (3, 6, 9). Although commercially
available effluent treatment systems work with high efficiency, their
high cost often prohibits financially poor countries from treating
their effluent before discharging it into the environment.
In this regard, two high-priority areas were identified that could
improve the prospects of implementation of pollution control measures,
namely, the use of indigenous resources and the use of inexpensive
materials to reduce the running cost. This study demonstrates (i) the
use of PVC supports that were fashioned from locally available flexible
conduit material used commonly in civil electrical wiring, (ii) the
ability of sodium acetate to sustain bacterial growth for biofilm
production, (iii) the use of wastewater modeled after mining effluent
in culture medium as a replacement for distilled water, and (iv) the
evaluation of thus-produced biofilm to filter Cu from defined (model)
wastewater. Copper is found in effluents from various industries,
including tanning, mining, metal processing and finishing,
electroplating, the automobile industry, and the pharmaceutical industry.
Filter matrix production: biofilm.
There are a number
of criteria that characterize a good biofilm support: large
surface-to-volume ratio, surface characteristics suitable for bacterial
attachment, and good porosity to permit unhindered flow of wastewater.
Glass materials have not been found to be good supports, as bacteria
have difficulty in attaching themselves to the smooth inert surface
(16). Although PVC is much better than glass, it is
superseded by fired clay and punched polyester (17). PVC
is more commonly used in treatment of wastewater by biological means,
and a variety of PVC supports have been developed specifically for this
purpose and are available commercially. Some of the purpose-built PVC
supports have been designed with grated surfaces to increase surface
roughness, which facilitates cell attachment (11).
Considering the economic restraints in Third World countries, the
biofilm support studied here was fashioned from flexible PVC conduit,
used commonly for civil electrical wiring, etc. Hollow cylinders
(approximately 13 mm by 12.7 mm [diameter]) were cut from
conduit and used as a support for immobilizing the bacterial biofilm
(Fig. 1A). The cylinders satisfied all of the criteria cited above, in having a large specific surface area (13,000 m2 m
3), good
porosity (96%), and suitable surface topology. The gross surface of PVC conduit was provided with grooves for flexibility (Fig.
1A), a characteristic that was expected to favor bacterial attachment.
Electron microscopy (see below for methodology) of the surface topology
revealed a rippled surface texture (Fig. 1B). The ripples resulted in
pits of approximately 1 to 1.5 µm by 0.5 to 0.75 µm, which
approximately matches the dimensions of the average bacillus cell.
Gjeltema et al. (8) have clearly demonstrated that biofilm
formation depends mainly on hydrodynamic conditions and particle
collisions in airlift reactors and also that increased surface
roughness promotes biofilm accumulation on suspended supports.

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FIG. 1.
Biofilm support. (A) Hollow cylinders (13 mm by 12.7 mm
[diameter]) cut from flexible PVC conduit. A cross-section through
the wall of the cylinder can be seen as a spirillum-like object near
the bottom of the panel. Length was measured by stretching a
longitudinal section of cylinder wall under a press to eliminate the
corrugation while the diameter was averaged from a large population of
measurements from one cutting edge to another. Bar, 1 cm. (B) The
support surface appears rippled under very-high magnification. Bar, 1 µm.
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A biofilm of
Pseudomonas aeruginosa strain CMG156 was
produced aerobically in 1 liter of stirred-tank chemostat during
continuous
culture at a dilution rate (
D) of 0.05 h
1 (µ
max, 0.32)
under carbon-limiting conditions (CH
3COONa) for
430 h at room temperature (

30°C). The culture medium was
prepared
in two parts, autoclaved separately (at 121°C for 15 min)
and
merged together when at room temperature. Part 1 consisted of
1.0 g of NH
4Cl, 0.2 g of
MgSO
4 · 7H
2O,
0.01 g of FeSO
4 · 7H
2O,
0.01 g of
CaCl
2 · 2H
2O,
5.0 g of CH
3COONa · 3H
2O, and 0.5 g of
yeast extract in 990 ml
of synthetic wastewater (with the pH adjusted
to 7.0 with 2 N NaOH).
Part 2 consisted of 0.5 g of
K
2HPO
4 in
10 ml of
distilled water and with the pH adjusted to 7.0. The
synthetic
wastewater used for medium preparation was modeled after
wastewater of
metal mining operations and included (in parts per
million) As (0.045),
Br

(<0.01), Cd (0.01),
Cl

(1,650), Co (1.2), Cr (<0.01), Fe (<0.01),
Na (2,050), Ni (0.88),
SO
42
(1,880), and Zn (0.1). Industrial applications requiring biomass
production require water as a major component in culture
media
along with ancillary services such as heating, cooling,
cleaning,
and rinsing (
15). The resultant biofilm
demonstrates the scientific
feasibility of such economizing
measures as use of wastewater
and of acetate as an economical carbon
source in culture
medium.
With an average thickness of 190 µm, the biofilm varied markedly in
depth and was found more frequently in grooves on both
outer and inner
surfaces of PVC cylinders (Fig.
2A).
Lack of biofilm
on ridges may be attributed to the liquid
shearing in chemostat.
High shear rates have been shown to result
in low biofilm growth
rates since the detachment rate can be
equivalent to or higher
than the biofilm growth rate (
1,
4,
13,
14). The maximum
thickness measured was 730 µm (from a number
of scanning electron
micrographs; data not shown here) whereas
biofilms produced artificially
(
12) or in natural
environments (
5) can range from 100 µm
to 3 mm;
therefore, significant improvements might be possible
from optimization
of the biofilm production process.

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FIG. 2.
Scanning electron micrographs of biofilm on PVC
cylinders. (A) Cross section through the wall of PVC support through
the groove region, seen here as a U-shaped object (against background
of the specimen mounting stub) colonized by biofilm, which appears as
crusts on the inner surface of the U shape. The U-shaped object is a
magnified region of the cross-sectional view shown in Fig. 1A. Bar,
1,000 µm. (B) This close-up view of biofilm near the apex of a ridge
on the surface of PVC support shows the extracellular matrix,
microchannels, and the slime layer. The surface of the PVC can also be
seen (in the lower right half of the panel). Bar, 10 µm.
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High-magnification scanning electron microscopy (SEM) (Fig.
2B) showed
an intercellular connective network that appears like
an extracellular
matrix (see below for methodology). Wherever
biofilm was found as a
thick crust, it appeared to be totally
covered by extracellular
polysaccharide. The role of extracellular
matrix in cell
aggregation is well known (
18). Microchannels
seen in Fig.
2B not only serve as a means of communication to
provide nutrients to
the inner depths of biofilm but also permit
the deeper regions of the
biofilm to accumulate metals that it
encounters in the liquid effluent.
For this reason the effective
surface area of a biofilm becomes much
greater than that of the
bare
support.
Bioreactor and copper biofiltration.
The biofilm was cultured
in two temporally spaced replications, pooled together, and packed into
Pyrex glass columns (40 cm by 5 cm [diameter]) capped by rubber
stoppers fitted with glass tubes to provide inlet and outlet ports for
the bioreactors. Unbuffered aqueous solution of
CuSO4 (6.39 mg liter
1)
was fed into the reactors by peristaltic pumps at 33 ml
h
1. Outflow from the bioreactors was measured
periodically for Cu concentration. A cell-free control column
was similarly analyzed in parallel. Each column had about a bed volume
of 528 ml and a fluid capacity of about 415 ml, with 150 cylinders
present in the bed. Copper was quantitatively measured by a
spectrophotometric method based on that of L. E. Macaskie
(10). The assay, scaled to be carried out directly in
1.5-ml disposable cuvettes, was modified to increase the sensitivity of
the reaction (1 ml) from a copper concentration from 7.98 mg
liter
1 down to 0.25 mg liter
1 by replacing
the water in Macaskie's method with a very dilute aqueous sample. To
100 µl of borate buffer [26.9 g of B(OH)3, 2.6 g of NaOH in 900 ml of distilled water adjusted to pH
8.1 with 2 M NaOH and made up to 1 liter] 20 µl of
reagent (0.5 g of bis-cyclohexanone-oxalyldihydrazone in 100 ml of 1:1 [vol/vol] water-ethanol, dissolved by heating and cooled
and filtered before use) was added, followed by addition of 880 µl of
aqueous sample, and the solution was mixed thoroughly. The colored
complex thus formed was measured at 595 nm against a standard copper
calibration curve prepared in a similar manner. The modified assay was
found to generate a linear curve in the range tested, i.e., 0.25 to 15 mg liter
1. The biofilm column was found to
possess 85% removal efficiency (Fig. 3);
on the whole the biofilm outperformed the control with twofold
efficiency.

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FIG. 3.
Effluent Cu after treatment with P.
aeruginosa CMG156 biofilm immobilized on PVC
cylinders. The bioreactor columns were challenged with aqueous Cu
solution (6.39 mg liter 1) at a flow rate of 33 ml
h 1. Symbols: , influent Cu; ×, effluent; ,
biofilm.
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SEM and X-ray microanalysis.
Biofilm-laden and control (i.e.,
without biofilm) PVC cylinders were cut into sections (2 by 3 mm),
air dried, fixed in glutaraldehyde for 1 h, dehydrated through
alcohol, critical point dried, mounted on stubs, sputter coated with
gold, and observed under an SEM. The Cu-exposed biofilm and
unexposed control biofilm were subjected to total elemental analysis by
using energy-dispersive X-ray microanalysis, which confirmed
accumulation of Cu in the biofilm and revealed hitherto-unknown
coaccumulation of Fe and Zn (Fig. 4).
Since Fe and Zn were not present in bioreactor influent
and since they were part of wastewater that was used to
prepare the culture medium, they were therefore taken up from the
culture medium. This demonstrates the multipurpose potential of the
biofilm.

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FIG. 4.
Coaccumulation of Cu, Fe, and Zn was determined by
energy-dispersive X-ray microanalysis of the biofilm exposed to Cu
(top) compared to no accumulation in unexposed biofilm (bottom). Peaks
of Au and Pd are a result of gold coating of the specimen.
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Uptake of metals from wastewater medium is disadvantageous since it may
prematurely saturate the biofilm during production.
On the other hand
biofilms produced in the presence of metals
may be more resistant to
higher metal concentrations. The latter
factor may be of importance in
situations in which the organisms
must be maintained in a viable state
to perform their intended
function. However, since the metal
accumulation mechanisms exploited
in this study do not depend on the
viability of cells, the use
of wastewater is therefore judged to be of
no advantage other
than that of reducing the requirement of distilled
water for biofilm
production. However, the presaturation problem may be
overcome
by desorbing metals from a fresh biofilm by means of dilute
acids
before using the biofilm in
filters.
Conclusion.
Inexpensive materials and cost-effective
techniques can be used to produce metal-removing biological filters
that function with reasonable efficiency. Although such methods may not
be the most optimized, they still might provide enough efficiency
to be of practical use to poor countries where pollution
generators are not able to afford the cost of conventional or
high-performance treatment facilities. Widespread small-scale on-site
applications of biological filters might provide a practical solution
to environmental problems in poor countries. Pollution, localized or
widespread, eventually has global consequences and is already present
in unmanageable proportions; therefore, control of pollution closest to
its source is the strongest countermeasure against its spread.
 |
ACKNOWLEDGMENTS |
We are most grateful to Geoffrey M. Gadd and Chris M. White of the
University of Dundee, Dundee, United Kingdom, for their invaluable
comments and especially for providing facilities for the electron
microscopy that was carried out by Martin Kierans and our Pakistani
colleagues Nazia Jameel and Jameela Akhtar who were visiting the
university at that time. We take this opportunity to thank the Sind
Institute of Urology and Transplantation, Karachi, Pakistan, and the
Biological Research Centre, University of Karachi, Karachi, Pakistan,
for providing some of the electron microscopy facilities.
This study was funded jointly by a research grant from the
Environmental Protection Agency (EPA), Karachi, Pakistan, and the laboratory-running grant from the University of Karachi.
 |
FOOTNOTES |
*
Corresponding author. Mailing address: Centre for
Molecular Genetics, University of Karachi, Karachi 75270, Pakistan.
Phone: 92 (21) 496-6045. Fax: 92 (21) 924-3190. E-mail:
a_nuzhat{at}yahoo.com.
 |
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Applied and Environmental Microbiology, September 2001, p. 4349-4352, Vol. 67, No. 9
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.9.4349-4352.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.