De novo synthesis refers to the synthesis of complex molecules from simple molecules such as sugars or amino acids, as opposed to recycling after partial degradation. For example, nucleotides are not needed in the diet as they can be constructed from small precursor molecules such as formate and aspartate. Methionine, on the other hand, is needed in the diet because while it can be degraded to and then regenerated from homocysteine, it cannot be synthesized de novo. De novo is a Latin phrase, literally translating to "from the new", but implying "anew", "from scratch", or "from the beginning."
De novolipogenesis is the process by which carbohydrates from the circulation are converted into fatty acids, which can by further converted into triglycerides or other lipids. Acetate and some amino acids can also be carbon sources for DNL. Normally, de novo lipogenesis occurs primarily in adipose tissue. But in conditions of obesity, insulin resistance, or type 2 diabetesde novo lipogenesis is reduced in adipose tissue and is increased in the liver. ChREBP is normally activated in the liver by glucose. Obesity and high-fat diets cause levels of carbohydrate-responsive element-binding protein in adipose tissue to be reduced. By contrast, high blood levels of insulin, due to a high carbohydrate meal or insulin resistance, strongly induces SREBP-1c expression in the liver. The reduction of adipose tissue de novo lipogenesis, and the increase in liver de novo lipogenesis due to obesity and insulin resistance leads to fatty liver disease. Fructose consumption activates both SREBP-1c and ChREBP in an insulin independent manner. Although glucose can be converted into glycogen in the liver, fructose invariably increases de novo lipogenesis in the liver, elevating plasma triglycerides, more than glucose. Moreover, when equal amounts of glucose or fructose sweetened beverages are consumed, the fructose beverage not only causes a greater increase in plasma triglycerides, but causes a greater increase in abdominal fat. DNL is elevated in non-alcoholic fatty liver disease, and is a hallmark of the disease. Compared with healthy controls, patients with NAFLD have an average 3.5 -fold increase in DNL. De novo fatty-acid synthesis is regulated by two important enzymes, namely acetyl-CoA carboxylase and fatty acid synthase. The enzyme acetyl CoA carboxylase is responsible for introducing a carboxyl group to acetyl CoA, rendering malonyl-CoA. Then, the enzyme fatty-acid synthase is responsible for turning malonlyl-CoA into fatty-acid chain. De novo fatty-acid synthesis is mainly not active in human cells, since diet is the major source for it. In mice, FAde novo synthesis increases in WAT with the exposure to cold temperatures which might be important for maintenance of circulating TAG levels in the blood stream, and to supply FA for thermogenesis during prolonged cold exposures.