Plastic pollution is one of the biggest environmental problems of the present time. Millions of tons of disposable one-use plastic has accumulated in our lands and seas due to its slow degradation rate. It is carcinogenic and it takes around 500 to 5000 years to degrade. In 2016, a group of
Evolution of Plastic Degrading Bacteria
Plastic pollution is one of the biggest environmental problems of the present time. Millions of tons of disposable one-use plastic has accumulated in our lands and seas due to its slow degradation rate. It is carcinogenic and it takes around 500 to 5000 years to degrade.
In 2016, a group of researchers led by Kohei Oda of Kyoto Institute of Technology and Kenji Miyamoto of Keio University discover Ideonella Sakaiensis (a plastic eating bacterium) originally isolated from a sample of PET-contaminated sediment near a plastic recycling facility in Sakai, Japan.
Being inspired by the above mentioned researchers, our objective is to evolve such a bacterium which has the ability to degrade PET plastic. The bacteria which are considered to evolve as the plastic degrading bacteria are those which do not have endospore formation process. The specification is due to the reason that the bacteria with endospore formation encapsulate their cell organelles into a capsule when there is lack of nutrition and do not consume unfavorable nutrition. Such bacteria are usually gram-positive.
We are supposed to gradually decrease the nutritional supply of the sample bacteria population and provide them culture medium such as agar added with plastic nano-particles. As bacteria has the ability to survive in all sorts of conditions, we hypothesize that in a struggle to survive, some of the sample bacteria population will learn to consume the PET plastic contaminated culture medium and then on PET plastic itself and consequently release such enzymes which can help to degrade plastic. The enzymes PETase and MHETase will be released by the bacteria to help in the breakdown of PET plastic nano-particles as expected. These enzymes will help to break the long chains of PET plastic particles into shorter chains or monomers.
We plan to iteratively culture and reculture the select population of bacteria that starts producing such enzymes, in a medium with greater proportions of PET plastic nano-particles, untill we have a population of evvoled bacteria that can thrive on PET plastic only.
This will help to increase the rates of decaying activity by increased enzyme release by the bacteria. Bacteria with no endospore formation volunteers in this process because it has the ability to survive in all sorts of conditions and low nutritional environments. To obtain it’s nutrition in the conditions of decreased growth medium the gram-negative (or bacteria with no endospore formation) try their level best for survival. The cultured sample will be provided with PET plastic nano-particles in increasing proportions. With time, the bacteria will start to degrade PET plastic nanoparticles for obtain their nutrition. This is how bacteria can help to degrade PET plastic. This can be implemented on a large scale as a solution to the increasing plastic waste threat.
The following are the objectives to be achieved.
Creating a laboratory environment that provides favorable conditions for the bacteria to thrive on plastic
This can be made possible by altering the nutritional intake of the bacteria by gradually increasing the amount of nanoparticles of PET plastic into the bacterial sustenance. We will observe that do the bacteria alters its chemical properties to help decompose plastic.
We will use gram-negative bacteria for this purpose as these bacteria do not have endospore formation. Such bacteria have the ability to alter their nutritional intake according to the provided growth media and try their best to strive. It is therefore expected that slowly and gradually the gram-negative bacteria will start consuming PET nanoparticles as it has the ability to adapt to all sorts of nutritional environment. Regularly providing PET nanoparticles will facilitate the bacteria to produce such chemicals/enzymes which will assist in the breakdown of plastic nanoparticles. The enzymes being produced may include MHETase and PETase (as expected) which will empower with time to work along with long chained particles, and if yes, we will find the decomposition rate which it provides. We will also find if there is a production of any toxic material during the process.
Steps to be followed:

Some of the benefits that can be achieved from the implementation of this project are:
Plastic pollution is one of the gravest environmental problems facing the Earth. Millions of tons of disposable one-use plastic have accumulated on the land, in the landfills, and in our oceans due to its extremely slow degradation rate. It takes around 500 to 5000 years to degrade. Our project will help to degrade the PET plastic in comparatively less time than the natural time required.
It can be very helpful to control marine pollution and help to save sea life as PET plastic accommodation is highly toxic for marine life as it is adding up into our food chain, as these marine species are later being utilized by humans. The consumption of such infected edible marine products is causing the production of chemicals like Bisphenol A and Dioxin which are really dangerous and even carcinogenic for human health. Proper disposal technique of PET plastic can help save the ecosystem.
At the end of our project, we expect to have samples of gram-negative bacteria which have evolved themselves as plastic degrading bacteria.
We will then find out the time required for such bacteria to hydrolyze the long chains of PET plastic polymers into smaller chains or monomers. The amount of sample being hydrolyzed will also be noted. And hence, we will find out the time estimate of degradation of a given amount of PET bottles in usual use with a given number of bacteria.
All this is aimed at developing a practically viable and environment friendly large scale facility of PET disposal.
| Item Name | Type | No. of Units | Per Unit Cost (in Rs) | Total (in Rs) |
|---|---|---|---|---|
| Electronic Microscope | Equipment | 1 | 49000 | 49000 |
| Laboratory glassware | Equipment | 34 | 170 | 5780 |
| Culture media | Equipment | 2 | 7610 | 15220 |
| Disposibles | Miscellaneous | 2 | 500 | 1000 |
| Transport | Miscellaneous | 20 | 300 | 6000 |
| Miscellaneous | 3 | 1000 | 3000 | |
| Total in (Rs) | 80000 |
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