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Wood waste - carbon source for Polyhydroxyalkanoates (PHAs) production
IJFWS
Wood waste - carbon source for Polyhydroxyalkanoates
(PHAs) production
Muthu Kumar. A
Forest and Wood Protection Division, Institute of Wood Science and Technology, Malleswaram, Bangalore, India- 560003
E-mail: touchurpearl@gmail.com, Phone no.: 0091-80-22190153, Fax no.: 0091-80-23340529
Polyhydroxyalkanoates (PHAs) are biodegradable and environmentally friendly bioplastics
accumulate as storage materials by various bacteria. These PHAs serve as energy and carbon
reserve materials for the bacteria. PHAs can be completely degraded within a span of 12-14
months by microbial consortia into CO2 and water. Wood waste as a carbon source for the
isolation and screening of polyhydroxyalkanoates (PHAs) accumulating bacteria was endeavored
during our study. Bacterial strains collected from various environmental sources were subjected
to culture studies for PHA synthesis. Pseudomonas lignicola was the single strain which was
able to synthesize PHA using the carbon source derived from wood waste, when compared to
other bacterial strains.
Keywords: Polyhydroxyalkanoates (PHA), bioplastics, carbon source, wood biomass, wood hydrolysate.
INTRODUCTION
Biological materials include chemically unrelated products
that are synthesized by microorganisms or part of them
under different environmental conditions (Alias and Tan,
2005). Bioplastics are an important class of biomaterials,
which was demarcated as polyesters that are broadly
dispersed in nature. These materials accumulate
intracellularly in microbes in the form of storage granules.
The physico-chemical properties of bioplastics look like
that of synthetic plastics, i.e., in terms of molecular weight,
brittleness, stiffness, melting point and other physical
properties PHA is comparable to some of the more
common petrochemical-derived thermoplastics. Because
PHAs are thermoplastics with biocompatible properties,
they are being developed as new absorbable materials for
implantable medical applications (Du and Yu, 2002). Other
applications of PHAs include packaging material,
osteosynthetic material in stimulation of bone growth, raw
material for production of stereo regular compounds
(PHAs being stereospecific), as mulch films in agricultural
fields and as hot melt adhesives (Reddy et al., 2003).
Precisely, Polyhydroxyalkanoates (PHAs) belong to the
polyoxoesters class of naturally occurring biopolymers
(Steinbuchel and Hein, 2001). Polyhydroxyalkanoates are
completely biodegradable synthesized by bacteria as
intracellular storage materials under conditions of stress
and act as carbon and energy reserve.
Polyhydroxyalkanoates (PHAs) are accumulated as
discrete granules to levels as high as 90% of cell dry
weight and are generally believed to play a role as sink for
carbon and reducing equivalents (Madison and Huisman,
1999).
Much effort has been devoted to reduce the price of PHAs
by development of bacterial strains, more efficient
Research Article
International Journal of Forestry and Wood Science
Vol.4(1), pp. 036-040, July, 2017. © www.premierpublishers.org. ISSN: XXXX-XXXX
Wood waste - carbon source for Polyhydroxyalkanoates (PHAs) production
Kumar M 037
fermentation and more economical recovery processes
(Godbole et al., 2003). High productivity is one of the major
factors for economical production of biodegradable
polymers (Chen et al., 2001). The carbon source should
be inexpensive since it is the major contributor to the total
substrate cost (Gao et al., 2002). Wood hydrolysate is a
potentially inexpensive and renewable feedstock that can
be produced through enzymatic or dilute acid hydrolysis of
cellulose or hemicellulose to fermentable sugars, such as
glucose, galactose, xylose, and mannose. Wood
hydrolysate has already been utilized for the production of
ethanol and xylitol. The isolation and development of
bacterial strains that can utilize such wood hydrolysates as
substrates is pursued intensively. In this regard the
present research work was focused on isolation and
screening of potential bacteria for synthesizing
polyhydroxyalkanoates (PHAs) using cheap carbon
source.
MATERIAL AND METHODS
Isolation of bacteria: Soil industrial effluent samples was
taken from Bommasandra Industrial Area (Paper & pulp) –
BIA and Kadugondana Halli (Tannery) – KH, Bangalore,
Karnataka, India were used for isolation of the bacteria.
Around 1.0 g of sample was serially diluted in sterile
distilled water and plated onto nutrient agar plates and
incubated at 30˚C for 24 hours. Various colonies of
different morphologies were individually picked and were
screened for PHA production, potential isolates were sub
cultured on nutrient agar plates as reported by Aarthi and
Ramana, 2011. The original cultures were maintained as
glycerol stock at –20°C for further use.
Rapid screening of native bacterial isolates for PHB
production: All the bacterial isolates were qualitatively
tested for PHB production by Nile blue (as a fluorescent)
staining method (Ostle and Holt, 1982). For rapid
screening of PHB producers, bacterial isolates were
spread into nutrient agar plate and the plates were
incubated at 30°C for 24 hours. Acetone solution of Nile
blue (0.5µg/ml) was spread over the colonies and the
plates kept undisturbed for 15 minutes.
Preparation of wood hydrolysate: Wood extracts
processing was carried out, for wood chips (at 160°C for
120 min), and hydrolysed with 2% sulphuric acid at 95°C
for 20 min., followed by concentration, neutralization, and
centrifugation for removal of precipitates (Chen et al.,
1984).
Analysis of wood hydrolysate for its contents: The
analysis of wood hydrolysate was performed with GC-MS
(JEOL GCMATE II GC-MS with Data system is a high
resolution, double focusing instrument, Maximum
resolution: 6000 Maximum calibrated mass: 1500 Daltons.
Source options: Electron impact {EI}, Chemical ionization
{CI}) for its knowing the actual sugar content of the source
material used for PHA bacteria.
Substrates for PHB production: Wood waste samples
was collected and dried in an oven at 60°C to reduce
moisture content and was milled into fine particles. The
following parameters such as reducing sugar, starch and
cellulose content in the raw seed were characterized (GC-
MS).
Bacterial Growth in specific media: Pure culture of
selected bacterial strain was revived in nutrient broth
initially and then grown in a defined Mineral Salt Media
(MSM) containing: 10g Hydrolyzed Seed, 5g Glucose, 5g
Sodium Chloride, 5g Di-Potassium Hydrogen Phosphate,
1g Potassium Chloride, 1g Magnesium Sulphate, and 1g
Ammonium Sulphate in 1L of distilled water. The pH of the
media was maintained to be 7.5±0.5. The culture flask was
kept in shaker at 150 rpm at 35 °C for two days (Amirul et
al., 2008, Du et al., 2001 and Yamanka et al., 2010).
Identification of PHA granules: The bacterial cells were
stained with Nile blue stain and visualized under UV
transilluminator (Geneflash, Syngene Bioimaging,
Cambridge, UK) and that gives a bright orange
fluorescence at a wavelength of 460nm. The accumulation
of PHA in the form of granules would be identified from the
fluorescing cells (Amirul et al., 2008).
RESULTS
Isolation of PHA producing bacteria
Polyhydroxyalkanoates (PHAs) are storage materials that
accumulate by various bacteria as energy and carbon
reserve materials. They are biodegradable,
environmentally friendly, and also biocompatible
bioplastics. Unlike petrochemical-based plastics that take
several decades to fully degrade, PHAs can be completely
degraded within a year by variety of microorganisms into
CO2 and water. Polyhydroxyalkanoic acids (PHAs) are
common intracellular compounds found in bacteria,
archaea, and in few eukaryotes such as yeasts and fungi.
PHAs are carbon and energy reserve polymers produced
in some microorganisms (e.g. Alcaligenes latus (FULAI
WANG AND SANG YUP LEE (1997)), Ralstonia eutropha
(Markus Potter, Mohamed H. Madkour, Frank Mayer and
Alexander Steinbuchel (2002)), Azotobacter beijerincki
(Soma PalA. MannaA.K. Paul (1999)), Bacillus
megaterium(GABRIEL J. MCCOOL AND MAURA C.
CANNON (1999)), when carbon source is in plentiful and
other nutrients such as nitrogen, phosphorus, oxygen or
sulfur are limited. Among the members of PHA family,
polyhydroxybutyrate (PHB) is the most common
biodegradable polymer and promising alternative to
synthetic non-degradable plastics. These polymers are
accumulated intracellular membrane enclosed inclusion
Wood waste - carbon source for Polyhydroxyalkanoates (PHAs) production
Int. J. For. Wood Sci. 038
Figure 1: (A) Isolate BIA 3 (refer Tab. No.1) from industrial effluents soil and (B) Isolate BIA 3 Figure 2: Culture plate of PHA producing
showing Fluorescence of PHA using Nile blue staining microorganism using Nile blue staining
Table 1: Characterization & Screening of PHA producing bacteria
S. No. Designation of Isolate Gram Reaction Shape
Plate Accumulation
Plate Count Nile Blue Staining
1 BIA 1 Gram Negative Cocci +++ +++
2 BIA 2 Gram Positive Cocci +++ ++
3 BIA 3 Gram Negative Small rod ++++ ++++
4 BIA 4 Gram Positive Cocci +++ +++
5 BIA 5 Gram Positive Dispersed rod +++ +++
6 KH 1 Gram Negative Small rod +++ +++
7 KH 2 Gram Negative Small rod ++ ++
8 KH 3 Gram Negative Dispersed rod + ++
9 KH 4 Gram Positive Cocci +++ +++
10 KH 5 Gram Positive Small rod ++++ +++
up to 90% of the cell dry weight under conditions of nutrient
stress and act as energy reserve material. These bacteria
have been reported from various environments, but only a
few from paper pulp and tannery effluents. For the rapid
detection and isolation of PHB producing bacteria, 0.02%
alcoholic solution of Nile blue A staining viable colony
method was used. The isolation of PHA producing bacteria
was done from paper pulp and tannery effluent water
samples. Most of the isolates showed positive result with
Nile blue A staining (Fig. No. 1). Both gram-positive and
gram-negative bacteria showed PHA production, but
gram-negative bacteria dominated the waste material
microflora of paper pulp and tannery industry.
The Nile Blue Staining method as experimented by Ostle
and Holt, 1982, was adopted visualizing PHA producing
microorganisms. The Nile blue was dissolved in acetone,
and was added to the agar medium for viable colony
staining. PHA producing microorganisms were visualized
as bright yellowish orange colonies under digital
microscope (Fig. No. 1B and 2).
Several bacteria were isolated from paper pulp and
tannery effluents by serial dilution method (Kumari Bhuwal
et al., 2013). From this, ten isolates were selected for PHA
production as shown in Table no. 1. Based on the intensity
of the fluorescence were observed in the Nile blue staining
method (Ostle and Holt, 1982), one potential PHA
producer (BIA 3) was screened out of ten isolates. The
granules showed Orange fluorescence under UV trans-
illuminator at a wavelength of 460nm as shown in Figures
1 - 2 and the results obtained was similar to Cortes et al.,
2008.
Characterization of wood hydrolysate
Hemicellulosic wood hydrolysate was analyzed by HPLC
and GC-MS to identify major carbon sources and inhibitory
compounds. The chromatographic profile of membrane
treated wood hydrolysate obtained by GC-MS is shown in
Fig. 3. Most of the pertinent peaks eluted within a retention
time of 20–30 min. Based on standards, the most
abundant peaks in the chromatogram were sugars,
including xylose, rhamnose, mannose, glucose, and some
minor sugar derivatives. Among the sugars, xylose was
the most abundant monosaccharide component, and
accounted for more than 85% of the total sugar content in
the hemicellulosic hydrolysate, followed by mannose,
rhamnose, and glucose (Table No. 2).
Chromatographic profile of membrane treated wood
hydrolysate obtained by GC-MS. Most of the pertinent
peaks eluted within a retention time of 18–35 min. Based
on standards, the most abundant peaks in the
Wood waste - carbon source for Polyhydroxyalkanoates (PHAs) production
Kumar M 039
Table 2: Composition of wood hydrolysate before and after membrane filtration
Substrates Before Membrane Treatment After Membrane Treatment
Xylose 170.7 g/L 70.7 g/L
Furfural 0.59 g/L N.D.
HMF 0.15 g/L 0.005 g/L
Acetate 0.78 m/L 0.05 m/L
Total phenolics (g/L GAE) 0.66 g/L 0.60 g/L
GAE – Gallic Acid Equivalent, N.D – Not Detected Molecular Weight cut-offs of 200 and 130 DA
Figure 3: Chromatogram of membrane-treated wood hydrolysate
Figure 4: Detection of PHA(B) produced by Pseudomonas lignicola under light microscope. (A) Bacterial
culture under light back ground (B) PHA bacteria under fluorescence back ground
chromatogram were sugars, including xylose, glucose and
other pentoses. Among the sugars, xylose was the most
abundant monosaccharide component, and accounted for
more than 80% of the total sugar content in the wood
hydrolysate, followed by glucose and rhamnose.
Identification of PHA granules
The accumulation of PHA in the form of granules would be
identified from the fluorescing cells as shown in figure 4.
Similar kind of studies was done earlier by Amirul et al.,
(2008) using fluorescence microscopy to visualize regions
of intracellular PHA accumulation.
DISCUSSION AND CONCLUSION
The isolation of PHA producing bacteria was done from
paper pulp and tannery effluent water samples. A large
proportion (%) of isolated bacteria produced PHA as
energy reserve material, proved by positive results with
Nile blue A staining. Both gram-positive and gram-
negative bacteria showed PHA production, but gram-
negative bacteria dominated the waste material microflora
of paper pulp and tannery industry. Hemicellulosic wood
hydrolysate was analyzed by HPLC and GC-MS to identify
major carbon sources and inhibitory compounds. The
chromatographic profile of membrane treated wood
Wood waste - carbon source for Polyhydroxyalkanoates (PHAs) production
Int. J. For. Wood Sci. 038
hydrolysate obtained by GC-MS, among the sugars,
xylose was the most abundant monosaccharide
component, and accounted for more than 85% of the total
sugar content in the hemicellulosic hydrolysate, followed
by mannose, rhamnose, and glucose. The accumulation of
PHA in the form of granules was identified from the
fluorescing cells (Amirul et al., 2008), using fluorescence
microscopy to visualize regions of intracellular PHA
accumulation. Detection of PHAs (B) produced by
Pseudomonas lignicola was visualized under light
microscope.
ACKNOWLEDGEMENTS
I sincerely thank The Director IWST for providing facilities
and moral support for completing the project, similarly I
would be grateful to ICFRE for sponsoring the project.
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Chen GQ, Zhang G, Park SJ, and Lee SJ, (2001).
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Chen LF, Lafayette W, Yang CM and Clark NJ, (1984).
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Du G, Che J, Yu J and Lun S, (2001). Continuous
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Alexander Steinbuchel (2002). Regulation of phasin
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stain for poly-beta-hydroxybutyrate.Appl. Environ.
Microbiol.; 44: 238–241.
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Technology; 87(2): 137-146.
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poly(β-hydroxybutyric acid) and exopolysaccharide by
Azotobacter beijerinckii WDN-01, World Journal of
Microbiology and Biotechnology; 15 (1): 11–16.
Steinbüchel A and Hein S, (2001). Biochemical and
molecular basis of polyhydroxyalkanoic acids in
microorganisms. Adv. Biochem. Eng. Biotechnol.
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hydroxybutyrate). Polym. Degrad. Stab.; 95: 1284-1292.
Accepted 3 August 2017
Citation: Kumar M (2017). Wood waste - carbon source
for Polyhydroxyalkanoates (PHAs) production.
International Journal of Forestry and Wood Science 4(1):
036-040.
Copyright: © 2017 Kumar M. This is an open-access
article distributed under the terms of the Creative
Commons Attribution License, which permits unrestricted
use, distribution, and reproduction in any medium,
provided the original author and source are cited.

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Wood waste - carbon source for Polyhydroxyalkanoates (PHAs) production

  • 1. Wood waste - carbon source for Polyhydroxyalkanoates (PHAs) production IJFWS Wood waste - carbon source for Polyhydroxyalkanoates (PHAs) production Muthu Kumar. A Forest and Wood Protection Division, Institute of Wood Science and Technology, Malleswaram, Bangalore, India- 560003 E-mail: touchurpearl@gmail.com, Phone no.: 0091-80-22190153, Fax no.: 0091-80-23340529 Polyhydroxyalkanoates (PHAs) are biodegradable and environmentally friendly bioplastics accumulate as storage materials by various bacteria. These PHAs serve as energy and carbon reserve materials for the bacteria. PHAs can be completely degraded within a span of 12-14 months by microbial consortia into CO2 and water. Wood waste as a carbon source for the isolation and screening of polyhydroxyalkanoates (PHAs) accumulating bacteria was endeavored during our study. Bacterial strains collected from various environmental sources were subjected to culture studies for PHA synthesis. Pseudomonas lignicola was the single strain which was able to synthesize PHA using the carbon source derived from wood waste, when compared to other bacterial strains. Keywords: Polyhydroxyalkanoates (PHA), bioplastics, carbon source, wood biomass, wood hydrolysate. INTRODUCTION Biological materials include chemically unrelated products that are synthesized by microorganisms or part of them under different environmental conditions (Alias and Tan, 2005). Bioplastics are an important class of biomaterials, which was demarcated as polyesters that are broadly dispersed in nature. These materials accumulate intracellularly in microbes in the form of storage granules. The physico-chemical properties of bioplastics look like that of synthetic plastics, i.e., in terms of molecular weight, brittleness, stiffness, melting point and other physical properties PHA is comparable to some of the more common petrochemical-derived thermoplastics. Because PHAs are thermoplastics with biocompatible properties, they are being developed as new absorbable materials for implantable medical applications (Du and Yu, 2002). Other applications of PHAs include packaging material, osteosynthetic material in stimulation of bone growth, raw material for production of stereo regular compounds (PHAs being stereospecific), as mulch films in agricultural fields and as hot melt adhesives (Reddy et al., 2003). Precisely, Polyhydroxyalkanoates (PHAs) belong to the polyoxoesters class of naturally occurring biopolymers (Steinbuchel and Hein, 2001). Polyhydroxyalkanoates are completely biodegradable synthesized by bacteria as intracellular storage materials under conditions of stress and act as carbon and energy reserve. Polyhydroxyalkanoates (PHAs) are accumulated as discrete granules to levels as high as 90% of cell dry weight and are generally believed to play a role as sink for carbon and reducing equivalents (Madison and Huisman, 1999). Much effort has been devoted to reduce the price of PHAs by development of bacterial strains, more efficient Research Article International Journal of Forestry and Wood Science Vol.4(1), pp. 036-040, July, 2017. © www.premierpublishers.org. ISSN: XXXX-XXXX
  • 2. Wood waste - carbon source for Polyhydroxyalkanoates (PHAs) production Kumar M 037 fermentation and more economical recovery processes (Godbole et al., 2003). High productivity is one of the major factors for economical production of biodegradable polymers (Chen et al., 2001). The carbon source should be inexpensive since it is the major contributor to the total substrate cost (Gao et al., 2002). Wood hydrolysate is a potentially inexpensive and renewable feedstock that can be produced through enzymatic or dilute acid hydrolysis of cellulose or hemicellulose to fermentable sugars, such as glucose, galactose, xylose, and mannose. Wood hydrolysate has already been utilized for the production of ethanol and xylitol. The isolation and development of bacterial strains that can utilize such wood hydrolysates as substrates is pursued intensively. In this regard the present research work was focused on isolation and screening of potential bacteria for synthesizing polyhydroxyalkanoates (PHAs) using cheap carbon source. MATERIAL AND METHODS Isolation of bacteria: Soil industrial effluent samples was taken from Bommasandra Industrial Area (Paper & pulp) – BIA and Kadugondana Halli (Tannery) – KH, Bangalore, Karnataka, India were used for isolation of the bacteria. Around 1.0 g of sample was serially diluted in sterile distilled water and plated onto nutrient agar plates and incubated at 30˚C for 24 hours. Various colonies of different morphologies were individually picked and were screened for PHA production, potential isolates were sub cultured on nutrient agar plates as reported by Aarthi and Ramana, 2011. The original cultures were maintained as glycerol stock at –20°C for further use. Rapid screening of native bacterial isolates for PHB production: All the bacterial isolates were qualitatively tested for PHB production by Nile blue (as a fluorescent) staining method (Ostle and Holt, 1982). For rapid screening of PHB producers, bacterial isolates were spread into nutrient agar plate and the plates were incubated at 30°C for 24 hours. Acetone solution of Nile blue (0.5µg/ml) was spread over the colonies and the plates kept undisturbed for 15 minutes. Preparation of wood hydrolysate: Wood extracts processing was carried out, for wood chips (at 160°C for 120 min), and hydrolysed with 2% sulphuric acid at 95°C for 20 min., followed by concentration, neutralization, and centrifugation for removal of precipitates (Chen et al., 1984). Analysis of wood hydrolysate for its contents: The analysis of wood hydrolysate was performed with GC-MS (JEOL GCMATE II GC-MS with Data system is a high resolution, double focusing instrument, Maximum resolution: 6000 Maximum calibrated mass: 1500 Daltons. Source options: Electron impact {EI}, Chemical ionization {CI}) for its knowing the actual sugar content of the source material used for PHA bacteria. Substrates for PHB production: Wood waste samples was collected and dried in an oven at 60°C to reduce moisture content and was milled into fine particles. The following parameters such as reducing sugar, starch and cellulose content in the raw seed were characterized (GC- MS). Bacterial Growth in specific media: Pure culture of selected bacterial strain was revived in nutrient broth initially and then grown in a defined Mineral Salt Media (MSM) containing: 10g Hydrolyzed Seed, 5g Glucose, 5g Sodium Chloride, 5g Di-Potassium Hydrogen Phosphate, 1g Potassium Chloride, 1g Magnesium Sulphate, and 1g Ammonium Sulphate in 1L of distilled water. The pH of the media was maintained to be 7.5±0.5. The culture flask was kept in shaker at 150 rpm at 35 °C for two days (Amirul et al., 2008, Du et al., 2001 and Yamanka et al., 2010). Identification of PHA granules: The bacterial cells were stained with Nile blue stain and visualized under UV transilluminator (Geneflash, Syngene Bioimaging, Cambridge, UK) and that gives a bright orange fluorescence at a wavelength of 460nm. The accumulation of PHA in the form of granules would be identified from the fluorescing cells (Amirul et al., 2008). RESULTS Isolation of PHA producing bacteria Polyhydroxyalkanoates (PHAs) are storage materials that accumulate by various bacteria as energy and carbon reserve materials. They are biodegradable, environmentally friendly, and also biocompatible bioplastics. Unlike petrochemical-based plastics that take several decades to fully degrade, PHAs can be completely degraded within a year by variety of microorganisms into CO2 and water. Polyhydroxyalkanoic acids (PHAs) are common intracellular compounds found in bacteria, archaea, and in few eukaryotes such as yeasts and fungi. PHAs are carbon and energy reserve polymers produced in some microorganisms (e.g. Alcaligenes latus (FULAI WANG AND SANG YUP LEE (1997)), Ralstonia eutropha (Markus Potter, Mohamed H. Madkour, Frank Mayer and Alexander Steinbuchel (2002)), Azotobacter beijerincki (Soma PalA. MannaA.K. Paul (1999)), Bacillus megaterium(GABRIEL J. MCCOOL AND MAURA C. CANNON (1999)), when carbon source is in plentiful and other nutrients such as nitrogen, phosphorus, oxygen or sulfur are limited. Among the members of PHA family, polyhydroxybutyrate (PHB) is the most common biodegradable polymer and promising alternative to synthetic non-degradable plastics. These polymers are accumulated intracellular membrane enclosed inclusion
  • 3. Wood waste - carbon source for Polyhydroxyalkanoates (PHAs) production Int. J. For. Wood Sci. 038 Figure 1: (A) Isolate BIA 3 (refer Tab. No.1) from industrial effluents soil and (B) Isolate BIA 3 Figure 2: Culture plate of PHA producing showing Fluorescence of PHA using Nile blue staining microorganism using Nile blue staining Table 1: Characterization & Screening of PHA producing bacteria S. No. Designation of Isolate Gram Reaction Shape Plate Accumulation Plate Count Nile Blue Staining 1 BIA 1 Gram Negative Cocci +++ +++ 2 BIA 2 Gram Positive Cocci +++ ++ 3 BIA 3 Gram Negative Small rod ++++ ++++ 4 BIA 4 Gram Positive Cocci +++ +++ 5 BIA 5 Gram Positive Dispersed rod +++ +++ 6 KH 1 Gram Negative Small rod +++ +++ 7 KH 2 Gram Negative Small rod ++ ++ 8 KH 3 Gram Negative Dispersed rod + ++ 9 KH 4 Gram Positive Cocci +++ +++ 10 KH 5 Gram Positive Small rod ++++ +++ up to 90% of the cell dry weight under conditions of nutrient stress and act as energy reserve material. These bacteria have been reported from various environments, but only a few from paper pulp and tannery effluents. For the rapid detection and isolation of PHB producing bacteria, 0.02% alcoholic solution of Nile blue A staining viable colony method was used. The isolation of PHA producing bacteria was done from paper pulp and tannery effluent water samples. Most of the isolates showed positive result with Nile blue A staining (Fig. No. 1). Both gram-positive and gram-negative bacteria showed PHA production, but gram-negative bacteria dominated the waste material microflora of paper pulp and tannery industry. The Nile Blue Staining method as experimented by Ostle and Holt, 1982, was adopted visualizing PHA producing microorganisms. The Nile blue was dissolved in acetone, and was added to the agar medium for viable colony staining. PHA producing microorganisms were visualized as bright yellowish orange colonies under digital microscope (Fig. No. 1B and 2). Several bacteria were isolated from paper pulp and tannery effluents by serial dilution method (Kumari Bhuwal et al., 2013). From this, ten isolates were selected for PHA production as shown in Table no. 1. Based on the intensity of the fluorescence were observed in the Nile blue staining method (Ostle and Holt, 1982), one potential PHA producer (BIA 3) was screened out of ten isolates. The granules showed Orange fluorescence under UV trans- illuminator at a wavelength of 460nm as shown in Figures 1 - 2 and the results obtained was similar to Cortes et al., 2008. Characterization of wood hydrolysate Hemicellulosic wood hydrolysate was analyzed by HPLC and GC-MS to identify major carbon sources and inhibitory compounds. The chromatographic profile of membrane treated wood hydrolysate obtained by GC-MS is shown in Fig. 3. Most of the pertinent peaks eluted within a retention time of 20–30 min. Based on standards, the most abundant peaks in the chromatogram were sugars, including xylose, rhamnose, mannose, glucose, and some minor sugar derivatives. Among the sugars, xylose was the most abundant monosaccharide component, and accounted for more than 85% of the total sugar content in the hemicellulosic hydrolysate, followed by mannose, rhamnose, and glucose (Table No. 2). Chromatographic profile of membrane treated wood hydrolysate obtained by GC-MS. Most of the pertinent peaks eluted within a retention time of 18–35 min. Based on standards, the most abundant peaks in the
  • 4. Wood waste - carbon source for Polyhydroxyalkanoates (PHAs) production Kumar M 039 Table 2: Composition of wood hydrolysate before and after membrane filtration Substrates Before Membrane Treatment After Membrane Treatment Xylose 170.7 g/L 70.7 g/L Furfural 0.59 g/L N.D. HMF 0.15 g/L 0.005 g/L Acetate 0.78 m/L 0.05 m/L Total phenolics (g/L GAE) 0.66 g/L 0.60 g/L GAE – Gallic Acid Equivalent, N.D – Not Detected Molecular Weight cut-offs of 200 and 130 DA Figure 3: Chromatogram of membrane-treated wood hydrolysate Figure 4: Detection of PHA(B) produced by Pseudomonas lignicola under light microscope. (A) Bacterial culture under light back ground (B) PHA bacteria under fluorescence back ground chromatogram were sugars, including xylose, glucose and other pentoses. Among the sugars, xylose was the most abundant monosaccharide component, and accounted for more than 80% of the total sugar content in the wood hydrolysate, followed by glucose and rhamnose. Identification of PHA granules The accumulation of PHA in the form of granules would be identified from the fluorescing cells as shown in figure 4. Similar kind of studies was done earlier by Amirul et al., (2008) using fluorescence microscopy to visualize regions of intracellular PHA accumulation. DISCUSSION AND CONCLUSION The isolation of PHA producing bacteria was done from paper pulp and tannery effluent water samples. A large proportion (%) of isolated bacteria produced PHA as energy reserve material, proved by positive results with Nile blue A staining. Both gram-positive and gram- negative bacteria showed PHA production, but gram- negative bacteria dominated the waste material microflora of paper pulp and tannery industry. Hemicellulosic wood hydrolysate was analyzed by HPLC and GC-MS to identify major carbon sources and inhibitory compounds. The chromatographic profile of membrane treated wood
  • 5. Wood waste - carbon source for Polyhydroxyalkanoates (PHAs) production Int. J. For. Wood Sci. 038 hydrolysate obtained by GC-MS, among the sugars, xylose was the most abundant monosaccharide component, and accounted for more than 85% of the total sugar content in the hemicellulosic hydrolysate, followed by mannose, rhamnose, and glucose. The accumulation of PHA in the form of granules was identified from the fluorescing cells (Amirul et al., 2008), using fluorescence microscopy to visualize regions of intracellular PHA accumulation. Detection of PHAs (B) produced by Pseudomonas lignicola was visualized under light microscope. ACKNOWLEDGEMENTS I sincerely thank The Director IWST for providing facilities and moral support for completing the project, similarly I would be grateful to ICFRE for sponsoring the project. REFERENCES Aarthi N and Ramana KV, (2011). Identification and characterization of polyhydroxybutyrate producing Bacillus cereus and Bacillus mycoides strains. Int. J. Environ. Sci.; 1: 744–756. Alias Z and Tan IKP, (2005). Isolation of palm oil-utilising, polyhydroxyalkanoate (PHA)-producing bacteria by an enrichment technique. Bioresour. Technol.; 96: 1229– 1234. Amirul A A, Yahya ARM, Sudesh K, Azizan, MNM and Majid, MIA, (2008). Biosynthesis of poly (3- hydroxybutyrate-10-4-hydroxybutyrate) copolymer by cupriavidus sp. VSMAA 1020 isolated from lake Kulim Malaysia. Bloresour. Technol.; 99: 4903-4909. Chen GQ, Zhang G, Park SJ, and Lee SJ, (2001). Industrial production of poly (hydroxybutyrate- cohydroxyhexanoate). Appl. Microbiol. Biotechnol.; 57: 50–55. Chen LF, Lafayette W, Yang CM and Clark NJ, (1984). Quantitative hydrolysis of cellulose to glucose using Zinc Chloride. United States Patent 4452640. Du G and Yu J, (2002). Green technology for conversion of food scraps to biodegradable thermoplastic polyhydroxyalkanoates. Environ. Sci. Technol.; 36: 5511-5516. Du G, Che J, Yu J and Lun S, (2001). Continuous production of poly-3-hydroxybutyrate by Ralstonia eutropha in a two stage culture system. J. Biotech.; 88: 59-65. Fulai Wang and Sang YL, (1997). Poly(3-Hydroxybutyrate) Production with High Productivity and High Polymer Content by a Fed-Batch Culture of Alcaligenes latus under Nitrogen Limitation, Applied and Env. Microb.; 3703–3706. Gabriel JM and Maura CC, (1999). Polyhydroxyalkanoate Inclusion Body-Associated Proteins and Coding Region in Bacillus megaterium, J. of Bacteriol.; 181(2): 585–592. Gao HJ, Wu Q and Chen GQ, (2002). Enhanced production of D-(3)-3- hydroxybutyric acid by recombinant Escherichia coli. FEMS Microbiol. Lett.; 213: 59–65. Godbole S, Gote S, Latkar M and Chakrabarti T, (2003). Preparation and characterization of biodegradable poly- 3-hydroxybutyrate-starch blend films. Bioresour. Technol.; 86: 33–37. Kumari BA, Singh G, Neeraj Kumar A, Goyal V, and Anita Yadav, (2013). Isolation and Screening of Polyhydroxyalkanoates Producing Bacteria from Pulp, Paper, and Cardboard Industry Wastes, International Journal of Biomaterials, Article ID 752821, 1-10. Maarten Kootstra, Hellen Elissen and Sander Huurman (2017). PHA’s (Polyhydroxyalkanoates): General information on structure and raw materials for their production, A running document for “Kleinschalige Bioraffinage; WP9: PHA”, Task 5, ACRRES - Wageningen UR, Report 727. Madison LL and Huisman GW, (1999). Metabolic engineering of poly (3-hydroalkanoates): from DNA to plastic. Microbiol. Mol. Biol. Rev.; 63: 21–53. Markus Potter, Mohamed H. Madkour, Frank Mayer and Alexander Steinbuchel (2002). Regulation of phasin expression and polyhydroxyalkanoate (PHA) granule formation in Ralstonia eutropha H16, Microbiology; 148: 2413–2426. Ostle AG and Holt JG, (1982). Nile Blue A as a fluorescent stain for poly-beta-hydroxybutyrate.Appl. Environ. Microbiol.; 44: 238–241. Reddy CSK, Ghai R, Rashmi and Kalai VC, (2003). Polyhydroxyalkanoates: an overview. Bioresource Technology; 87(2): 137-146. Soma Pal A and Manna AK Paul (1999). Production of poly(β-hydroxybutyric acid) and exopolysaccharide by Azotobacter beijerinckii WDN-01, World Journal of Microbiology and Biotechnology; 15 (1): 11–16. Steinbüchel A and Hein S, (2001). Biochemical and molecular basis of polyhydroxyalkanoic acids in microorganisms. Adv. Biochem. Eng. Biotechnol. 71: 81-123. Yamanaka K, Kimura Y, Aoki T and Kudo T, (2010). Effect of ethylene glycol on the end group structure of poly (3- hydroxybutyrate). Polym. Degrad. Stab.; 95: 1284-1292. Accepted 3 August 2017 Citation: Kumar M (2017). Wood waste - carbon source for Polyhydroxyalkanoates (PHAs) production. International Journal of Forestry and Wood Science 4(1): 036-040. Copyright: © 2017 Kumar M. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are cited.