Production and characterization of PHA from recombinant E. coli harbouring phaC1 gene of indigenous Pseudomonas sp. LDC-5 using molasses

INDUSTRIAL MICROBIOLOGY

Production and characterization of PHA from recombinant E. coli harbouring phaC1 gene of indigenous Pseudomonas sp. LDC-5 using molasses

Saranya V.; Shenbagarathai R^*

PG and Research Department of Zoology and Biotechnology, Lady Doak College, Madurai, India

ABSTRACT

Polyhydroxyalkanoates (PHA) are biodegradable and biocompatible green thermoplastics, synthesized by wide variety of bacteria as an intracellular carbon and energy storage intermediate. They are used as an alternative to nonrenewable petroleum derived plastics. The current interest in these biopolyesters is stimulated by the search for cost-effective capitalized production. This paper attempts to achieve maximized production rate from recombinant system using inexpensive substrate. Molasses from agro-industrial waste was used to produce PHA from recombinant E.coli in batch culture. PHA yield in molasses (3.06g/L ± 0.05-75.5%) was higher than that of sucrose (2.5g/L ± 0.05 - 65.1%). Properties of the polymer produced from molasses and sucrose were analyzed by DSC, TGA, DTA, GC/MS, TLC and optical rotation studies. The findings suggested that molasses enhanced PHA production in recombinant E.coli.

Key words: Polyhydroxyalkanoates, molasses, cost effective production.

INTRODUCTION

Polyhydroxyalkanoates (PHAs) are optically active polyesters of natural origin (15). It is synthesized in micro-organisms as intracellular carbon reserve material during the excess of carbon under nitrogen limiting conditions. It can be utilized by micro-organism as a reserved material at the time of its need (13). As it has material properties (Molecular weight, Melting temperature, Glass transition temperature) similar to synthetic polymers (24), it is trusted to triumph over the problems and harmful effects of plastic wastes (3, 16, 22). Owing to these features, PHAs have drawn much attention for numerous industrial applications.

A major limitation to achieve marketable production of PHAs is their higher price than synthetic fossil fuel based plastics. The high production cost is the most important barrier hindering PHA to compete the market with conventional synthetic polymers. For instance, Zeneca Bio Products (Billingham, UK) produced approximately 1,000 tons per year of PHB/V copolymer at ca. US $ 16/kg. The price of conventional petrochemical plastics is less than US $ 1/kg (11, 23). To achieve successful commercialization of PHA, economic production system must be sort out. As the cost of raw material (substrate, bacterial strain) is one of the major factors influencing the economy of production (18, 20), the present study is concentrated on the cost effective production of PHA by combining the use of inexpensive substrate (molasses) for the growth of the potential strain.

Information on Physio - chemical material property is obligatory for the possible usage of polymer. For example, PHA that is semi-crystalline, with low melting point (T_m), high elongation to break can be used for biomedical applications. Based on these above said concerns, the present study is focused on to achieve lower production cost using molasses as substrate for recombinant strain and characterization of material properties of PHA to ensure quality product for medical application.

MATERIALS AND METHODS

Bacterial strain and Growth conditions

Recombinant E.coli harboring phaC1 of Pseudomonas.sp.LDC-5 (18, 19) was used in this study. The purity of the strain was ascertained by repeated streaking on LB medium. It was grown in PHA accumulating RC medium (8,18) supplemented with 1% carbon source when needed.

Carbon Substrate

PHA production was studied using the molasses (dark brown in colour) obtained from sugar refinery mill, Madurai District (India). For comparative assessment expensive carbon substrate, sucrose (Himedia) was used.

Fermentor Studies

PHA production was achieved by using lab scale fermentor. Seed cultures were inoculated into sterilized minimal media (RC) supplemented with inexpensive / expensive substrates. Fermentation was carried out using 3.5 L Bio console ADI (025) Fermentor (Applikon Biotechnology (Holland). Parameters used for operation: pH (7.0), dissolved oxygen content (30%), agitation speed (3000g) and temperature (37ºC). The pH was maintained robotically by the addition of 0.5M NaOH and 0.5M HCl. Coconut oil mixed with water (1:1) was used as the anti foaming agent.

Polymer Recovery

Cultured broth was centrifuged at 8000 g for10 min and the pellet was washed thoroughly with distilled water (19,7). PHA was extracted from the cells as per the method of Sujatha et al (2006). The recovered PHA was subjected to further analysis.

Thin Layer Chromatography Analysis of Polyhydroxyalkanoates

50µL sample of 48 h grown cells was spotted on to TLC plate prepared using silica gel and allowed to run in the solvent system consisting of ethyl acetate and benzene (1:1) for 40 min. For identification of PHA, TLC plate was kept inverted in a beaker containing iodine solution (Himedia) in a water bath (100ºC) for 5 - 10 min for saturation of iodine vapors. The yellowish green spots indicate the presence of PHA (9).

Thermal analysis of polymeric samples

Polymeric samples of approximately 2mg were encapsulated in an aluminum pan and placed in a Differential Scanning Colorimeter (DSC) chamber for analysis (TA INSTRUMENTS SDT Q600 V 8.3BUILD 101) (CECRI, Karaikudi). The samples were heated up to 1000ºC at a rate of 20ºC per minute under Nitrogen atmosphere. Data were analyzed by THERMAL ADVANTAGE Software. The melting temperature (Tm) was determined from the peaks of DSC endotherms (14). Thermal characterization by Thermo Gravimetric Analysis (TGA) and Differential Thermal Analysis (DTA) of recovered polymer was conducted with TA INSTRUMENTS SDT Q 600 V 8.3 BUILD 101 at 1000ºC at a rate of 20ºC per minute under Nitrogen atmosphere. Alumina was used as reference sample.

Derivatization of polymeric samples

5 mg of polymer sample was mixed with 2 mL of 3.0% (v/v) sulfuric acid in methanol and 2 mL of chloroform, and the mixture was refluxed for 3.5 h at 100ºC to convert monomer units to their corresponding ethyl ester (1). The mixture was cooled and washed with 10 mL of distilled water. The organic phase was collected and dried over MgSO₄ and used for further analysis.

GC-MS analysis

For molecular analysis of the methyl esters, a coupled GCMS was performed using a GC Clarus 500 Perkin Elmer, with Elite-1(100% Dimethyl poly siloxane) capillary column (30 mm × 0.25 mm × 1 µm; carrier gas - He, 1 mL/min.; temperature program - 110ºC for 2 min then increased at 5ºC/min to 280ºC and maintained) equipped with a Turbo mass gold model mass selective detector (PPRC, Tanjore). The mass spectra obtained were compared with the NIST '98 Mass Spectral Library with Windows Search Program version 2.1, National Institute of Standards and Technology (US Department of Commerce) with electron energy of 70 eV and mass scan (m/z) 45-50.

RESULTS AND DISCUSSION

Biosynthesis of polymer

The influence of substrate (molasses and sucrose) on the growth and PHA production by recombinant E.coli harboring phaC1 of Pseudomonas.sp.LDC-5 was investigated. The presence of bright spherical PHA granules in the cells were clearly demonstrated by phase contrast light microscope (OLYMPUS-DP12-CX41) (Figure 1). The PHA yield was increased when molasses (3.06g/L± 0.05-75.5%) was used as carbon source than with sucrose (2.5g/L ± 0.05 - 65.1%). Figure 2 illustrates the kinetics of the production.

The enhanced PHA production in molasses could be attributed by the composition of the substrate. The C:N ratio has led to unbalanced nutrient condition, which in turn had led to inhibition of TCA cycle enzymes such as citrate synthase and isocitrate dehydrogenase and consequently have slowed down the TCA cycle. As a result, the acetyl co-A routed to PHA biosynthesis (2). Figure 3 depicts that the production cost using molasses is relatively lower compared to sucrose.

TLC identification of PHA

PHA components were identified with the characteristic appearance of yellowish green colour spot in the TLC plates. The retention factor (R_f) was 0.58 for both the samples in accordance with reports of Paul et al (2004).

DSC analysis of PHA

Melting temperature (T_m) is determined from endothermal peaks of the DSC thermograms. PHA recovered from the strain cultured with molasses had T_m of 129.59 º C (Figure 4a) is indeed lower than that with sucrose (T_m 152 º C) (Figure 4b). T_m is influenced by the length of side chain and functional groups present (5). Lower T_m indicates that the side chains are longer. Molasses had incorporated longer side chains in comparison with sucrose. The range of T_m reported in this study suits fabrication of product as per ASTM: D 882-91 test (21).

 

TGA & DTA analysis of PHA

Thermal stability of PHA is important for their melt processing. The temperature at 5 % weight loss termed T_d(5%) was employed to evaluate polymer thermal stability. PHA samples recovered from recombinant strain cultured with molasses had T_d(5%) of 240 ºC (Figure 5a). The PHA sample from the strain cultured with sucrose had T_d(5%) of 310ºC (Figure 5b). T_d(5%) was much higher than T_m reflecting thermal permanence. This validates the improved avenues for polymer processing (21).

DTA helps to determine the heat of reaction of decomposition process. If cross linking reactions occurred during degradation of PHA, an exothermic peak would be detected in DTA thermogram. The temperature at which cross linking occurs is the curing temperature. The curing temperature for cost effectively produced PHA is around 431ºC. This stands to be a valid property as major barrier for commercial application of PHA, was their thermal instability due to lack of ability to cross-link (10).

Examination of Optical rotation

The optical rotation of methyl ester of PHA from molasses as well as sucrose grown cells was negative (-1) which indicates that R form is enantiomerically excess in accordance with earlier reports (6).

GC-MS analysis of PHA

GC-MS analysis helps in elucidating the structure of components. The key compounds of concern were identified based on their retention peak. PHA from recombinant E.coli cultured with molasses significantly contained C₉H₂₀O₃ (Propane - 1, 1 triethoxy-) and C₁₂H₂₆ (Dodecane) (Figure 6). These compounds signify that the monomer chains were of biodegradable polyester family (11). Characteristic fragment at m/z 103 suggested the presence of hydroxyl group of carbon 3 formed by cleavage of alpha to the hydroxylated carbon (12). This had made apparent that financial prudence effort had no way compromised the eminence of artifact.

PHA recovered from sucrose grown cultures had significant compounds like C₁₂H₂₄O₃ (Dodecanoic acid 3-hydroxyl-) and C₁₄H₃₀ (Tetradecane) (Figure 7).These are biodegradable by virtue of hydrolysable ester bonds (4). The components identified had served as evident for the verity that nutrient and culture conditions modify the side chain length.

PHA production by recombinant E.coli harboring phaC1 gene was studied using molasses as nutrient substrate, indeed to lower the production cost. Its effect on properties was tracked and it's now evident that molasses as a substrate did not adversely affect material properties and in fact had led to betterment. This study will lead to economic PHA production appropriate for large scale intended for commercialization.

ACKNOWLEDGEMENT

Thanks to the financial support by DBT, India vide project reference "BT/PR 10211/ BCE/08/615/ 2007", DBT-BIF and "BT/PR11256/PID/06/450/2008". Dr.Sujatha is thankfully acknowledged for providing the strain. Support of Dr. Peterselvanayagam, Dr.Binu Ramesh, Dr.Mahalakshmi, Mrs. Poornimak kani, Ida, Abirami, Priyadarsini, Suguna, Rajeswari, Asnet Mary and Poorna is thankfully accredited.

Submitted: December 31, 2009; Returned to authors for corrections: December 09, 2010; Approved: May 16, 2011.

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Publication Dates

• Publication in this collection
  21 Dec 2011
• Date of issue
  Sept 2011

History

• Received
  31 Dec 2009
• Accepted
  16 May 2011
• Reviewed
  09 Dec 2010