While our bodies run on both fats and carbohydrates as primary fuel sources, carbohydrates are the body’s preferential unit of energy due to their ability to be efficiently converted to energy and their lack of adequate storage capacity in comparison to fat. Carbohydrates are derived from various sources, such as grains, legumes (beans), corn, fruit, dairy, and vegetables. Not all sources are equal; carbohydrate sources can be divided into the following three categories: sugar, starch, and fiber.



Sugar, the common base unit of all carbohydrate molecules, is comprised of six carbon atoms, twelve hydrogen atoms, and six oxygen atoms. This base unit is known as a monosaccharide (“one-sugar”) or a simple carbohydrate. The three basic monosaccharides, glucose, fructose, and galactose, are building blocks for the formation of the majority of carbohydrates. Monosaccharides can combine together to form disaccharides (two sugars). The three most common disaccharides are sucrose (table sugar), lactose (dairy sugar), and maltose (beer sugar). Sucrose is formed by combining glucose and fructose, lactose by glucose and galactose, and maltose by glucose and glucose. At the disaccharide level, carbohydrates are still referred to as “sugar”.

Combining these sugar molecules can result in larger carbohydrates that vary in molecular makeup and mechanism of digestion. Before moving to the other two classes of carbohydrates, let’s further discuss the different structures that we see among carbohydrates.


When forming chains of monosaccharide sugars, each monosaccharide is linked in either alpha or beta configurations. The alpha configuration is easily digested by gut enzymes, whereas the beta configuration is not easily broken down by gut enzymes.


Carbohydrates can also be classified by the bonds that hold their sugar molecules together. Bonds called glycosidic bonds can join two sugar molecules together by linking one of the six carbon atoms on one sugar to one of the six carbon atoms on another sugar. The most common types of glycosidic bonds are alpha-1,4 and alpha-1,6. Below is an example of an isomalto-oligosaccharide (IMO) that contains both bonds.


The molecular configurations of carbohydrates determine their digestive capabilities. Alpha-1,4-glycosidic bond can be easily broken down by digestive enzymes; however, an alpha-1,6-glycosidic bond is slightly digestive resistant. This affects the internal response to the digestion of the carbohydrate.

Carbohydrates, depending on their configuration, are broken down into glucose when they are digested. An increase in blood glucose stimulates the release of insulin from the pancreas. Insulin allows for the uptake of glucose into the cells of the body. This can be thought of as a lock and key mechanism, where insulin receptors are locks, and insulin is the key that can unlock the cell to release glucose. Some carbohydrates stimulate a quicker and more robust insulin response than others. This is where the glycemic index comes into play. The glycemic index is based on how rapidly carbohydrates raise blood sugar and thereby stimulate the release of insulin from the pancreas. On a scale of 0-100 the highest glycemic index of 100 is the rate at which pure glucose increases blood sugar. High glycemic carbohydrates are rapidly digested and converted into glucose, resulting in a rapid increase in blood glucose levels. Lower glycemic carbohydrates, due to their beta bonds and/or alpha-1,6 glycosidic bonds, result in a slower release of glucose. Glucose, once inside the cell, can either provide immediate energy or be stored.


Now that we have looked at the differences in the molecular structures of carbohydrates and how these differences affect their digestibility, let’s move from disaccharides to oligosaccharides. The prefix “oligo-” denotes units of 3-10, hence oligosaccharides are comprised of 3-10 units of monosaccharides and are considered to be “complex” carbohydrates. Polysaccharides are long-chain monosaccharides consisting of greater than 10 units; polysaccharides can potentially be thousands of units long. Starch is considered to be a polysaccharide and is typically comprised of alpha-1,4 glycosidic bonds. Starch is the most abundant polysaccharide in plants and yields four calories per gram. Common sources of starch are corn, potatoes, rice, tapioca, and wheat. Despite being considered a “complex” carbohydrate, oligo- and polysaccharides are still broken down into glucose during digestion.


The final carbohydrate source is fiber. Much discrepancy exists regarding what constitutes a fiber. For our purposes we will use the following definition: plant material not digested by mammalian enzymes. It is the inability of fiber to be broken down that provides it unique characteristics and benefits. Fiber can be classified based on its linkage as well as by its physiological properties. Most fibers are made up of beta bonds, which if you recall are digestive-resistant. The physiological properties that classify fiber are soluble or insoluble. A possible fate of undigested carbohydrates is fermentation by gut bacteria, a process which leads to the production of short chained fatty acids (acetate, propionate, and butyrate) and gasses (hydrogen, carbon dioxide, and methane) which can benefit the gut microbiome and provide energy. We will discuss this in more detail in a future article on fiber.


Fiber, with its beta bonds, can also trap starches and prevent them from being digested. This results in what is known as “resistant starch.” Resistant starches are starch fractions that are resistant to enzymatic hydrolysis. They pass through the small intestine in resistance to digestive enzymes and behave similarly to fiber. Resistant starches are similar to that of regular starch in physical characteristics. In regard to biochemical characteristics, resistant starches have a high gelatinization temperature similar to that of fiber but do not have the water-absorbing properties that fiber has (1).


Resistant starches can be found in raw starches, such as potatoes or bananas, as well as certain foods like grains, seeds, and legumes. Resistant starch can also be formed via the cooking and cooling of starch foods, such as potatoes (2). Resistant starches may have a role in ketogenic dieting because they are digestive-resistant and thus cannot be metabolized into energy-producing compounds (e.g. glucose). However, more research needs to be conducted in this area.

Resistant starches can provide an array of health benefits, including improved insulin sensitivity and blood glucose levels (3,4). Below is a list of additional potential benefits of resistant starch.

Carbohydrates and Ketogenic Dieting

Certain carbohydrate sources should be avoided when ketogenic dieting, as their carbohydrate content per serving and/or glycemic index is too high for ketosis. In general, if the goal is to stay in ketosis, where the body is producing and utilizing ketones for energy, carbohydrate consumption should likely be kept at or below five percent of total calories. Within this five percent, the majority of the carbohydrate sources should be very high fiber, cruciferous vegetables. Sugar, fruit, milk, grains, legumes, and starchy vegetables (potato, yucca root, corn, etc.) generally cannot be consumed on a ketogenic diet. Vegetable sources such as broccoli, cauliflower, spinach, mushrooms, and kale can be consumed on a ketogenic diet. For a guide on what carbohydrates you should eat, check out our Ketogenic Stoplight.

Fiber and Ketogenic Dieting

Acquiring adequate dietary fiber can be difficult when carbohydrates are restricted. For this reason, it is important for a ketogenic dieter to focus on fiber intake. Additionally, fiber can alleviate some of the complications that may arise in ketogenic dieters. Due to the delayed glucose response that accompanies meals containing fiber, a high fiber intake may be beneficial for maintaining stable blood glucose levels, which we know is important on a ketogenic diet.

Fiber can be incorporated into the diet via the consumption of cruciferous vegetables or supplementation. High-fiber protein bars are becoming common among  low-carbohydrate dieters since the carbohydrates they contain theoretically should not elicit a glucose or insulin response, but this is only the case if the appropriate fiber is used.


IMOs, typically used in high-fiber protein bars, possess both 1,4 and 1,6 glycosidic bonds. This means that part of the molecule can be digested at the 1,4 bond, while the 1,6 bond is digestive-resistant. For this reason, IMOs are classified as fibers despite possessing some starch characteristics. Certain IMOs could be classified as resistant starch based on the inability of their glycosidic bonds to be broken. The digestive capability of the 1,4 bond allows this particular carbohydrate to elicit an insulin response, which may make soluble corn fiber a better option over IMOs. Soluble corn fiber is comprised primary of alpha 1,6 glycosidic bonds, making it highly digestive resistant, which in turn results in much lower blood glucose levels and subsequently a lower insulin response (5).





Keto Conclusions

  • Carbohydrates are complex structures that can be classified as either sugars, starches, or fiber.
  • Different carbohydrate sources are managed by the body differently depending on their molecular makeup.
  • While ketogenic dieting, sugars and non-resistant starches should be avoided and fiber should make up most of the total daily carbohydrate intake.