A Glance at Food Nutrition Components Analysis
Taizhu Li
Beijing Royal School, Beijing, China
Keywords: Food Nutrients, Protein, Fat, Sugar.
Abstract: With the development of economic, food safety gradually becomes an obvious part drawing our attention in
life. As we all know, the food nutrients show closely connection to our human health. Sugar and fat are key
players in diabetes, cardiovascular and cancer diseases and millions of people are suffering these diseases.
Protein plays a vital role in our body as well, especially for the infants for whom the milk is their main source
of energy supply so the quality of these food should be paid tightly attention to. In food industry, the food
analysis methods should be diverse, and many well-established approaches already worked well for a long-
time history, while during this time new and fantastic techniques always emerging and become a strong
competes to the conventional ways. In this article, we will attempt to gather the existing analysis approaches
for the main food components and show their advantages and disadvantages.
1 INTRODUCTION
The nutritional contents of food are closely related to
human health. Food contains a variety of nutrients
needed by the human body, including sugar, fat,
protein and so on. In terms of their functions in the
body, these nutrients are divided into three parts:
constituent substances, energy substances and
regulating substances. In the nutritional composition
of various foods, only certain components are the
same, and the content of these components in various
foods is also very different. Therefore, a variety of
foods can be combined from these food ingredients,
which is the composability of food ingredients. It is
precisely because of the combinability that the
inherent differences of various foods are created.
With the development of economic, humans
gradually noticed that nutrients in food are needed to
pay more attention since we all know that all the
nutrients are closely to human health. According to
this, the industry adopts many hash policy to control
the quality of the food to ensure the food safety. From
this view, it is important to develop many useful and
efficient technique to detect and quantify all the
components in food. Due to the differences and
complexity of the food matrix, the methods used to
detect food ingredients are also diverse, such as
chromatography, colorimetry, refraction, and so on.
But these methods have their own advantages and
disadvantages. With the rapid development of science
and technology, the research of food nutrients is
gradually deepening, and food testing technology and
testing instruments are constantly updated and
developed. This enables modern food testing to cope
with various complex situations. This article includes
the current detection methods of common nutrients in
food and their advantages and disadvantages.
2 PROTEIN DETECTION
Typically, the Western Blot (WB) has been used as a
traditional way to detect protein(Taylor and Posch
2014). The principle of WB is based on the antibody
recognition, and specific band will be got for each
specific protein in which quantification is an essential
to verify the expression level of each protein (Figure
1 and 2). However, the time costs of this approach are
usually 1-2 days which is a disadvantage when
compared to others. Even though the approach was
improved recently to shorten the time to several
hours(Lin-Moshier and Marchant 2013), the way that
WB is able to detect several proteins not the total
protein contents still make WB not as a popular one
used in food protein contents detection.
So for a long time, total nitrogen content was used
to the determine the protein content of foods in which
Kjeldahl invented a method that has been used
broadly to determine the total nitrogen content. But
the method still costs a relative long time, researchers
356
Li, T.
A Glance at Food Nutrition Components Analysis.
DOI: 10.5220/0011370100003438
In Proceedings of the 1st International Conference on Health Big Data and Intelligent Healthcare (ICHIH 2022), pages 356-361
ISBN: 978-989-758-596-8
Copyright
c
2022 by SCITEPRESS Science and Technology Publications, Lda. All rights reserved
mainly focused on the time costa to improve the
process to make it more efficiently. Recently, a
developed method based on an automated
instrumental technique was applied in food protein
contents detection since it is capable of measuring the
food protein concentration in a shorter time than
Kjeladahl methods(Stitcher, Jolliff et al. 1969, Wiles,
Gray et al. 1998). Even though the technique was
developed recently, the technique is based on
Dumas’s method which was created over a century
ago. It is already on its way to compete with the
Kjeldahl method since it costs a shorter time without
the loss of accuracy.
Figure.1: Typical western blot image for probing three different proteins1.
Figure.2: Typical western blot workflow(graph from Creative Biolabs).
A Glance at Food Nutrition Components Analysis
357
3 NUCLEOTIDE DETECTION
Nucleotide is one of the most important biological
molecular in nature, although it is not a nutrient in
food, it is vital to identify some nucleotides which can
be used as markers to some specific species, since
bacterial infection can be very harmful to human
health. In order to control the contaminations of
bacteria, some nucleotide as markers should be
detected in food industry.
Polymerase chain reaction (PCR) is a
conventional technique to amplify the small segments
of DNA, allowing us to have a large amount of DNA
to detect(White, Arnheim et al. 1989).the specificity
of PCR relies on oligonucleotide primers which are
complementary to both ends of the target sequence.
PCR typically involves two sequential amplification
reactions, in which each uses a different pair of
primers. The product of the first amplification
reaction is used as a template for the second PCR,
which is initiated by the oligonucleotides placed
inside the first pair of primers. Applying two pairs of
oligonucleotides makes more cycles to be performed,
thereby improving the sensitivity of PCR. (Rychlik
1993)
After the PCR is done, the product is separated in
a gel and confirm the size of the product so that we
can verify that the contents of nucleotide from
bacteria or some specific species. However, the whole
process usually takes several hours, and the gel
separation must be used to confirm the size and the
amount of the nucleotide. In order to simplify the
whole process and get a better way to quantify the
amount of the DNA, real-time PCR (RT-PCR)
(Figure 3 and 4) was developed to be applied in the
quantification of DNA(Kubista, Andrade et al. 2006).
Fluorescent probes are added in the RT-PCR
system when the reaction is done, the amount of DNA
can be calculated at once. So all the whole process is
completed only in one step as a result that the RT-
PCR is applied broadly in DNA quantification.
4 FAT DETECTION
Fat plays a very important role in human health since
excessive fat from food can increase the risks of
obesity and metabolic disorders in our body thus
causing serious health problems. Obesity is a very
common, severe, and costly disease. In United States,
obesity prevalence was 42% in 2017 2018 and the
number is 30% in 1999-2000. This disease always
happens with other severe diseases such as heart
disease, stroke, and certain types of cancer, leading to
huge medical costs to people and government. So,
more attention should be paid to the fat contents in
food. The meaning of total fat is total lipids, including
phospholipids(Holm and Wretlind 1976).
The commonly used techniques are Soxhlet
analysis and acid/alkaline hydrolysis(Khoshtinat,
Koohy-Kamaly et al. 2021). This method is based on
an AOAC Official Methods of Analysis (AOAC).
The first step of it is acid hydrolysis and sample
drying, and then sequentially, the extraction itself on
a Soxhlet device in which the whole process costs
about couple of hours.
A new method relied on an innovative
microwave-assisted extraction (MAE) approach
makes the determination of total fat in cheese
samples. MAE method is statistically equivalent to
other methods, showing good performance and
allows the determination of total fat in 12 samples
simultaneously in 100 min, which shows a much
faster and easier handling than Soxhlet(Adeel, Zuber
et al. 2018).
Figure 3: The steps of RT-PCR(graph from MyBioSource).
ICHIH 2022 - International Conference on Health Big Data and Intelligent Healthcare
358
Figure 4: Typical results of RT-PCR(graph from Wikimedia).
Figure 5: HPLC-ELSD profile of fructose, glucose, and sucrose standard compounds
14
.
5 SUGAR DETECTION
Sugars are caloric and sweet tasting which occur
ubiquitously in our life, including vegetables, honey,
and fruits. Human beings are born with the
preference for sweet taste. Lactose, a type of sugar
naturally existing in milk, in breast milk ensures that
this mainly source of nutrition for babies is palatable
and acceptable. While in food most of the sugars are
chemically added which are monosaccharide or
disaccharide carbohydrates imparting sweet taste. Lot
of foods contain some of each.
Sugars are ones of carbohydrate, and like other
carbohydrates they also contain carbon, oxygen, and
hydrogen molecules. Carbohydrates play an
important role in a healthy diet, as do proteins, fats,
and water. In addition to dietary fiber, in the
condition that carbohydrates are consumed, they will
be digested and broken down to glucose, serving as
an energy source for most organs in whole
body. Glucose is a better source of energy for blood
A Glance at Food Nutrition Components Analysis
359
cells, the central nervous system, and the digestion
system.
Fructose, glucose, and galactose are very common
monosaccharides in which common disaccharides
include sucrose, maltose, and lactose. Quantification
of sugars are now determined by couple of methods.
They include enzymatic method which measures
sucrose phosphorylation and hydrolysis of fructose
and glucose(Finney, Danehower et al. 2005) or
measuring absorbance growth based on commercial
standard assay of sugar kit(Hurtta, Pitkanen et al.
2004). In addition to mentioned above, High
Performance Liquid Chromatography (HPLC)
approach coupled with refractive index detector
(RID) or evaporative light scattering detector (ELSD)
are used as well. HPLC-ELSD shows many
advantages especially for its compatibility, stability,
and sensitivity with gradient elution when compared
to HPLC-RID. Recently, developments in gas
chromatography-mass spectrometry (GC-MS)
equipment and techniques have made this technique
becoming helpful in compositional and structural
analysis of oligomers, polymers and
monosaccharides, especially in food industry and life
sciences areas.
6 CONCLUSIONS
Protein, fat and sugar are the main nutrients in food,
which provide the energy supply to human body.
With the development of technique, many detection
approaches were well established for the past couple
of years, all of this ensure the food safety and make
the food components clear to customers which can
help them know clear about the food components and
have the authority to decide to have them or not.
In recent years, food testing and analysis
technology has developed rapidly, but due to the
limitations of sample pre-processing technology or
the defects of the instrument method itself, many
testing technologies are only at the qualitative or
semi-quantitative level, and the accuracy of the
results needs to be further improved. For example,
continuously improve the detection equipment,
increase the sensitivity and accuracy of the detection
equipment, and optimize the pre-processing methods,
so that the detection results reach an accurate level.
At the same time, actively research and discuss
various advanced detection methods and technologies
according to the continuously developing food types
and develop rapid analysis technologies that can
simultaneously achieve high-efficiency sample pre-
processing and sensitive follow-up detection to meet
the urgent needs of today's food analysis.
In addition to the technique this regard, industry
and the authority should also pay more attention to
the laws in this area so that lot of illegal events can be
avoided. Also customers should also learn more in
order to be able to identify the food label in a good
view.
So for a long time, total nitrogen content was used
to the determine the protein content of foods in which
Kjeldahl invented a method that has been used
broadly to determine the total nitrogen content. But
the method still costs a relative long time, researchers
mainly focused on the time costa to improve the
process to make it more efficiently. Recently, a
developed method based on an automated
instrumental technique was applied in food protein
contents detection since it is capable of measuring the
food protein concentration in a shorter time than
Kjeladahl methods(Stitcher, Jolliff et al. 1969, Wiles,
Gray et al. 1998). Even though the technique was
developed recently, the technique is based on
Dumas’s method which was created over a century
ago. It is already on its way to compete with the
Kjeldahl method since it costs a shorter time without
the loss of accuracy.
REFERENCES
Adeel, S., et al. (2018). "Microwave-assisted extraction and
dyeing of chemical and bio-mordanted cotton fabric
using harmal seeds as a source of natural dye." Environ
Sci Pollut Res Int 25(11): 11100-11110.
Finney, M. M., et al. (2005). "Gas chromatographic method
for the analysis of allelopathic natural products in rye
(Secale cereale L.)." J Chromatogr A 1066(1-2): 249-
253.
Holm, I. and A. Wretlind (1976). "Methods for complete
intravenous nutrition with fat." Acta Chir Scand Suppl
466: 62-63.
Hurtta, M., et al. (2004). "Melting behaviour of D-sucrose,
D-glucose and D-fructose." Carbohydr Res 339(13):
2267-2273.
Khoshtinat, K., et al. (2021). "Comparative study of salt,
total fat and sugar contents of mayonnaise and salad
dressings from the Iranian market." East Mediterr
Health J 27(5): 452-458.
Kubista, M., et al. (2006). "The real-time polymerase chain
reaction." Mol Aspects Med 27(2-3): 95-125.
Lin-Moshier, Y. and J. S. Marchant (2013). "A rapid
Western blotting protocol for the Xenopus oocyte."
Cold Spring Harb Protoc 2013(3).
Rychlik, W. (1993). "Selection of primers for polymerase
chain reaction." Methods Mol Biol 15: 31-40.
ICHIH 2022 - International Conference on Health Big Data and Intelligent Healthcare
360
Stitcher, J. E., et al. (1969). "Comparison of Dumas and
Kjeldahl methods for determination of nitrogen in
feces." Clin Chem 15(3): 248-254.
Taylor, S. C. and A. Posch (2014). "The design of a
quantitative western blot experiment." Biomed Res Int
2014: 361590.
White, T. J., et al. (1989). "The polymerase chain reaction."
Trends Genet 5(6): 185-189.
Wiles, P. G., et al. (1998). "Routine analysis of proteins by
Kjeldahl and Dumas methods: review and
interlaboratory study using dairy products." J AOAC
Int 81(3): 620-632.
A Glance at Food Nutrition Components Analysis
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