The biodiesel sector has witnessed tremendous growth in recent years, leading to a significant increase in glycerol production as a by-product. Addressing the challenge of glycerol valorization is crucial for the sustainability of the biodiesel industry. One promising solution is the conversion of glycerol into more valuable chemicals, such as 1,3-propanediol (1,3-PDO). Microorganisms offer several advantages for this conversion process, including their diverse metabolic pathways and enzymatic capabilities. Key enzymes involved in the 1,3-PDO production pathway include glycerol dehydratase (GDHt), glycerol dehydratase reactivase (GDHtR), and 1,3-propanediol dehydrogenase (1,3-PDDH). The aim of the present research project was to bio-transform glycerol into 1,3-propanediol by cloning and expressing GDHt and 1,3-PDDH in E. coli. Additionally, the specific activity of GDHt enzyme and the necessity of GDHtR were investigated. The selected genes dhaB, orfX, and orfZ from Klebsiella pneumoniae were utilized for the synthesis of GDHt, GDHtR, and 1,3-PDDH, respectively. Initial measurements of GDHt’s activity revealed detectable levels, which increased upon the addition of GDHtR, indicating the influence of GDHtR on GDHt's activity. However, the interpretation of activity values is complicated by potential interferences from aldehydes or metabolites present in crude cell extracts. To address these complexities, enzyme assays using purified enzymes were performed, but no statistically significant data were obtained. Further investigations are required to optimize the measurement of GDHt activity and address the potential influence of the cofactor B12. Coexpression of GDHt and 1,3-PDDH enzymes, resulted in a reduction of cofactor NADH, indicating the potential conversion of glycerol into 1,3-PDO. Nevertheless, the formation of the product could not be detected, and the decline in NADH could not be solely attributed to the coupled-enzymatic reaction. Additional investigations, The production of biodiesel, a type of renewable fuel, has been increasing rapidly, leading to a significant increase in the production of glycerol by-product. Scientists are now looking for ways to use this excess glycerol in a sustainable manner. One exciting solution is to convert glycerol into a valuable chemical called 1,3-propanediol (1,3-PDO). 1,3-PDO is a valuable compound with various applications in industries like manufacturing, textiles, and cosmetics. It can be used to make polyester fibers, which are used in clothing and fabrics, as well as in the production of personal care products like lotions and creams. This conversion process of glycerol into 1,3-PDO can be done by using microorganisms, like bacteria, which have special abilities to transform glycerol into 1,3-PDO. To make this conversion happen, certain enzymes are involved. Enzymes are special proteins which help carry out specific chemical reactions inside the cells. In the case of glycerol transformation, two key enzymes are responsible for the process: glycerol dehydratase (GDHt) and 1,3-propanediol dehydrogenase (1,3-PDDH). Here's how the transformation of glycerol into 1,3-PDO occurs: First, GDHt takes glycerol and converts it into a different chemical called 3-hydroxypropionaldehyde (3-HPA). Next, 3-HPA goes through another reaction facilitated by 1,3-PDDH, resulting in the formation of 1,3-PDO. In this research project, these two enzymes were used to transform glycerol into 1,3-PDO. The focus was on studying GDHt and 1,3-PDDH enzymes and how they work together. A common bacterium called Escherichia coli (E. coli) was used, and the genes responsible for making GDHt and 1,3-PDDH were inserted into these bacteria, to produce the enzymes. When GDHt and 1,3-PDDH were produced together in a single bacterial cell, there was an indication that glycerol was being transformed into 1,3-PDO. However, the actual production of 1,3-PDO couldn’t be detected, and there were other factors affecting the me