| The best  agents degrade bacteria would be biological life forms such as bacteria which  multiply by the millions in days and are themselves completely biodegradable. It  is towards this challenge that research has been going on, and the latest  effort which shows some success has been published in the March 11, 2016 issue  of Science by a Japanese group, led by Dr Kanji  Miyamoto of Keio University, Kanagawa. The group concentrated on looking for  and identifying bacteria from the PET bottle recycling sites, and found one  such microbe that they have named Ideonella  sakaiensis (the first name  identifies the family and the second honors the geographic location where they  found the bacterium). I. sakaiensis sticks  to the surface of the PET bottle, secretes one molecule which they named  PET-ase (the suffix “– ase” denotes an enzyme molecule), which breaks down PET  into a smaller building block abbreviated as MHET. MHET is now taken up and  broken down by another enzyme in the microbe’s cell (called MHET hydrolase) and  hydrolyzed to produce ethylene glycol and terephthalic acid- the two small  molecules (called monomers). The I sakaiensis  is highly efficient as a safe  biodegradable agent. Two interesting points emerge from the Japanese work. One  is: can we now isolate the ethylene glycol and terephthalic acid, the two  monomers, and reuse them to make PET? This offers a nice self-contained set up  where the PET bottles and plastics discarded after use are biodegraded back to  the starting materials in a bio-reactor, and then taken to the polymer  synthesizing unit which remakes the PET. The other point is more challenging  and surely there are molecular biologists already working on it. That is: why  not clone the genes that express the enzyme PET-ase and MHET hydrolase into  some other properly chosen microbe (other than I.sakaiensis ), using genetic engineering methods  and thus attempt to biodegrade PET. 
 E.  coli, a common gut  bacteria, can be engineered to produce biodegradable polymers for use in  surgical sutures, among other applications.A Korean  research team has engineered gut bacteria to create non-natural polymers in a  biorefinery; allowing various plastics to be made in an  environmentally-friendly and sustainable manner. The research was published in Nature Biotechnology.  In the present study, a team headed by Distinguished Professor Lee Sang Yup of  the Korea Advanced Institute of Science and Technology (KAIST) adopted a  systems metabolic engineering approach to develop a microorganism that can  produce various non-natural polymers which have biomedical applications. According  to the researchers, this approach is the first successful example of biological  production of poly(lactate-co-glycolate)  (PLGA) and several novel copolymers from renewable biomass by one-step direct  fermentation of metabolically engineered Escherichia coli (E. coli)  bacteria. The researchers drew inspiration from the biosynthesis process for  polyhydroxyalkanoates, biologically-derived polyesters produced in nature by  the bacterial fermentation of sugar or lipid. From there, they designed a  metabolic pathway for the biosynthesis of PLGA through microbial fermentation  directly from carbohydrates in E. coli strains. PLGA is a biodegradable,  biocompatible and non-toxic polymer. PLGA has been widely used in biomedical  and therapeutic applications such as surgical sutures, prosthetic devices, drug  delivery, and tissue engineering. In order to produce PLGA by microbial  fermentation directly from carbohydrates, the team incorporated external and  engineered enzymes as catalysts to co-polymerize PLGA while establishing a few  additional metabolic pathways for the biosynthesis to produce a range of  different non-natural polymers. This bio-based synthetic process for PLGA and  other polymers could substitute for existing complicated chemical production  methods. Lee and his team has also managed to produce a variety of PLGA  copolymers with different monomer compositions such as the US Food and Drug  Administration-approved monomers 3-hydroxyburate, 4-hydroxyburate, and  6-hydroxyhexanoate. Newly applied bioplastics such as 5-hydroxyvalerate and  2-hydroxyisovalerate were also made
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