Lecture 3- Feed Chemistry Flashcards

1
Q

What does feed analysis consist of?

A

• Assessment of nutrient composition of feeds • Evaluate (potentially) availability of nutrient content of a feed (chemical integrity) • Ensure that dietary nutrient supply matches human or animal requirements for nutrients – a key issue in formulation chemistry -what are we looking at when doing a feed analysis? -just because a chemical is there does not mean it is available for the animal to use -crucial that the nutrients match the requirements of the species in that stage

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2
Q

What are the two main developments in laboratory analysis of feed?

A

• 1. Chemical evaluation: try to determine the chemical content of the feed • 2. In vitro methods: try to replicate what happens in the digestive system so to understand what will happen in the body

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3
Q

What is the feed analysis called?

A

-proximate or Weende analysis -standard method for feed composition

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4
Q

How does the feed analysis (proximate) divide nutrients in food?

A

• Partitions nutrients into five major fractions • Dry matter (DM) – basis of feed formulation (important to know since it tells us in what percentage of the feeds are there nutrients) • Crude Protein (CP) – sources of nitrogen • Ether extract (EE) – lipids and related compounds • Crude Fibre (CF) – structural and non structural CHO (carbohydrates) • Total ash (TA) – mineral matter • Nitrogen-free extract (NFE)

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5
Q

What is the Dry matter (DM) component in feed analysis?

A

• Heat sample in oven @ 105oC overnight % Dry matter =

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6
Q

What is the use of dry matter data?

A

• DM is the denominator for all nutrient contents of feeds. • DM is the basis of all formulation and rationing of animals. • DM does not provide information on the association of water to the feed particle – an important issue in water and mineral nutrition • Losses during drying do not always relate to loss of water per se and can reflect the concentration of volatile and fermentation compounds (e.g. silage)

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7
Q

What is the crude protein component of feed analysis?

A

-2. methods of estimating crude protein in feed, the Kjeldahl and the Dumas (LECO) method -1:• Kjeldahl method • Boil sample in concentrated (36 N) sulphuric acid [converts all nitrogen into (NH4)2SO4] • NH3 is liberated from the (NH4)2SO4 by adding 12N NaOH and steam distillation • NH3 is trapped into boric acid or sulphuric acid (0.02N), and the titrated using standard acid ———- • Method assumes that all nitrogen comes from protein containing (16% N) • Crude protein = N × 6.25 (100/16) -way of estimating protein content: -assumes all N exists as protein, which is not so -then multiply N by 6.25 (assuming that all protein contains 16% of N)

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8
Q

What is the second method of estimating crude protein in feed?

A

• Dumas (LECO) method • Vapourisation of sample to its constituent elemental components and determine the concentration of N • Recalculate CP content by multiplication of N x 6.25 • Suffers from similar problems to Kjeldahl methods -newer and quicker method

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9
Q

What are the problems associated with the two methods of estimating the crude protein content of feed?

A

• Problems associated with two methods • Not all N comes from protein other sources (free amino acids, amines and nucleic acids) • Ignores N from nitrates and nitrites • Amino acid composition of foods and feeds are variable and therefore %N in feed protein varies considerable. This leads to a variation in the coefficient 6.25 (eg. 6.38 for milk) • Over or under estimates protein content of feed • Analytical problems – incomplete capture of N (volatile N compounds)

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10
Q

What is an indirect assesment of crude protein content of feeds?

A

• Use of near infra-red spectrometry (NIRs) is a rapid method for determining the crude protein content of a feed. • Estimation of true protein is also feasible using NIRs and the feed does not require pre-treatment to precipitate the protein (e.g. classical methods use trichloroacetic acid to precipitate protein before Kjeldahl assessment. -new method: rapid method, you measure the infrared reflectance of the the feed and from that get protein -using this to determine the nutrient content and availability of the content -all you need to have is calibrated standards to which to compare

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11
Q

What do you use crude protein data for?

A

• Used as a basis for feed formulation • Provides no information on the availability of protein to digestion •Provides no information on essential amino acid -composition just by measuring the crude protein content we don’t know the amino acids in the feed, the animal doesn’t have a requirement for protein as such, it needs specific amino acids (the essential amino acids) in a particular ratio -it also doesn’t provide us with an estimate of the availability -lysine is the most limiting, as it is found at low levels of lysine in grains relative to other amino acids -we need to dig deeper

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12
Q

How do you measure EE the ether extract?

A

• Measure of fat content • Continuous extraction (4 -6 hours) with petroleum ether using reflux apparatus • Residue after solvent evaporation = ether extract • EE

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13
Q

Does ether extract analysis provide fat analysis?

A

• Ether extract does not provide information on the composition of fat • Generally, fat composition (chain length and degree of saturation) is determined using gas-liquid chromatography (GLC) • Ether extract methods do not provide information on essential fatty acids • Some fats are “volatile” e.g. short chain (C2, C3 and C4) and can be lost to analysis if care is not taken. -often it is particular fatty acids that we are interested in

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14
Q

What is the total ash component of feed analysis and how is it done?

A

• Residue after combustion of organic constituents • Procedure: • Ignite sample at 550oC in a muffle furnace until all organic matter is removed • Problems: • Fraction still contains sulphur and phosphorus •

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15
Q

What are the issues with total ash?

A

• Total ash method does not differentiate between mineral matter, soil and silica content. • Silica content is determined as acid insoluble ash – a useful parameter in passage rate studies • Soil content is generally determined at total titanium content

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16
Q

What is the crude fibre component of feed analysis?

A

• Crude fibre represents structural carbohydrates or cell wall constituents • CF = cellulose + hemicellulose + pectin + lignin • Ruminants (eg. Cattle, sheep) are better able to digest plant fibre than monogastrics (eg. humans, pigs) • Procedure • Boil sample in 1.25% H2SO4, filter and then boil the residue in 1.25% NaOH. Residue is dried and ashed. CF = difference between filtered dried sample and ash -particularly important in ruminants as they can digest fibre, as they have rumen and the microbial population in there can digest cellulose etc.

17
Q

What does crude fibre constitute?

A

• Crude fibre represents structural carbohydrates or cell wall constituents • CF = cellulose + hemicellulose + pectin + lignin • Ruminants (eg. Cattle, sheep) are better able to digest plant fibre than monogastrics (eg. humans, pigs) • Procedure • Boil sample in 1.25% H2SO4, filter and then boil the residue in 1.25% NaOH. Residue is dried and ashed. CF = difference between filtered dried sample and ash -feed boiled in weak acid and then filtered= to mimic digestion

18
Q

What are the problems with crude fibre analysis?

A

• Problems • Mimics gut pH conditions (acidic stomach & alkaline intestinal), ignores but enzymatic digestion • CF is not “real” fibre in the true sense and is practically meaningless • Underestimates fibre: some true fibre (especially hemicellulose, pectin and lignin) is solubilised during extraction • Phased out in most laboratories, replaced by the detergent fibre system -so it underestimates the true fibre

19
Q

What is the nitrogen free extract (NFE) component of feed analysis?

A
  • Approximates non-structural carbohydrate content (starch and sugars)
  • Determined by the difference between total dry matter and the sum of the other four chemical components
  • estimates starches and sugars: -it does it by difference - not measure just do the other ones and what is left
  • • NFE is the only part of proximate analysis not determined directly
  • NFE supposedly represents the soluble carbohydrate fraction of a feed as crude fibre is the “insoluble” carbohydrate fraction
  • NFE contains accumulated errors from the estimation of DM, CP, CF, EE and total ash

-every issue with the other measurements accumulates here as we use those results

20
Q

What is the summary of proximate analysis of feed?

A

-get wet feed (or normal condition), we determine the water content by the dry analysis and from the dry feed we determine the chemical constituents

21
Q

What are the total digestible nutrients (TDN)?

A
  • TDN= -multiply factor for EE as fat has high energy content
  • from this we know more about the energy the animal is actually getting
  • dCP = digestible CP
  • dCF = digestible CF
  • dNFE = digestible NFE
  • EE = ether extract
  • TDN is a link from chemical analysis to energy content of a feed
22
Q

What are the estimated digestion coefficients?

A

• Crude protein= 75.0 • Crude fiber = 73.9 • Nitrogen-free extract 80.6 • Ether extract= 53.9 -not all that we eat is digested -these are approximates, differs between individuals, feeds, physiological states -almost 1/2 of the fat that is consumed is excreted

23
Q

An example of calculating TDN:

A
  • Calculation of TDN of field beans for ruminant feeding
    1. 86 grams per 100g of dry matter that the animal digests
24
Q

What are the assumptions of TDN?

A

• The EE extracts digestible lipids only • All dietary N is contained in protein with a N content of 16% (assumes relationship between CP and N is 6.25) • Crude fibre represents the digestible fibre fraction of the feed • NFE represents the soluble and digestible carbohydrate fraction • None of the assumptions are true and, more importantly, do not reflect digestive or feed processes. • The assumption that crude fibre contains all dietary cellulose, hemicellulose and lignin is one of the most serious problems with the system • The TDN system was replaced by the Detergent fibre system developed by PJ van Soest.

25
Q

What is a new method for performing fibre analysis?

A

• Conceptually subdivides total carbohydrate fraction • Cell wall

26
Q

What are in vitro digestion methods?

A

• In vitro digestion • Tilley-Terry (2 stages) • Rumen digestion • 48 h incubation in rumen fluid at 39 C • Gastric digestion • 48 h incubation of residue in pepsin solution at pH 2 -in vitro= in glass -tilley- terry: simulate rumen digestion an dthen the gastric digestion -get sample of rumin fluid, put it in, and incubate (the fluid will have all the micorbes usually present) -then you add pepsin solution and simulate what happens in the stomach of the ruminant -if you do both stages get an approximate simulation of ruminate digestion

27
Q

What are in vitro gas production methods?

A

• A popular new method for evaluation of feeds • A method that models rumen fermentation by measurement of gas production from the feed substrate • Further analysis can be used to examine stoichiometry of the reaction (VFA, ammonia and gas quality assessments) • Future analysis will examine microbial community structure -another method, rather than measuring the amount of starch that disappears, get the amount of gas that is produced