4.7 Article

A method of assessing essential amino acid availability from microbial and ruminally undegraded protein in lactating dairy cows

Journal

JOURNAL OF DAIRY SCIENCE
Volume 104, Issue 2, Pages 1777-1793

Publisher

ELSEVIER SCIENCE INC
DOI: 10.3168/jds.2020-18248

Keywords

dairy cow; microbial protein; amino acid availability; stable isotope

Funding

  1. Virginia Agricultural Experiment Station (Regional Research Project
  2. Blacksburg, VA) [NC-2040]
  3. Hatch Program of the National Institute of Food and Agriculture, USDA (Washington, DC)
  4. College of Agriculture and the Life Sciences Pratt Endowment at Virginia Tech (Blacksburg, VA)
  5. Balchem Corp. (Covington, VA)
  6. China Scholarship Council (Beijing, China)

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The study aimed to assess the availability of 6 essential amino acids (EAA) from microbial protein (MCP) using stable isotope techniques, finding that 45% of absorbed EAA came from MCP, influenced by starch and rumen-degradable protein (RDP) in diets. The absorption rates of EAA were calculated from plasma enrichment and varied across different amino acids.
The objective of this study was to extend a stable isotope-based assessment of AA absorption from rumen-degradable protein (RDP) sources to include determination of essential AA (EAA) availability from microbial protein (MCP). To demonstrate the technique, a study using a 2 x 2 factorial arrangement of treatments applied in a repeated 4 x 4 Latin square design was undertaken. Factors were high and low rumen-degradable protein and high and low starch. Twelve lactating cows were blocked into 3 groups according to days in milk and randomly assigned to the 4 treatment sequences. Each period was 14 d in length with 10 d of adaption followed by 4 d of ruminal infusions of N-15-labeled ammonium sulfate. On the last day of each period, a C-13-labeled AA mixture was infused into the jugular vein over a 6-h period to assess total AA entry. Rumen, blood, urine, and milk samples were collected during the infusions. Ruminal bacteria and blood samples were assessed for AA enrichment. Total plasma AA absorption rates were derived for 6 EAA from plasma C-13 AA enrichment. Absorption of 6 EAA from MCP was calculated from total AA absorption based on N-15 enrichment in blood and rumen bacteria. Essential AA absorption rates from total protein, MCP, and rumen-undegradable protein were derived with standard errors of the mean of 6, 14, and 14%, respectively. An average of 45% of absorbed EAA were from MCP, which varied among 6 EAA and was interactively affected by starch and RDP in diets. Microbial AA availability measured by isotope dilution method increased with the high RDP diets and was unaffected by starch level, except for Met, which decreased with high starch. Microbial protein outflow, estimated from urinary purine derivatives, increased with RDP and was not significantly affected by starch. This was con-sistent with measurements from the isotope dilution method. Total AA absorption rates measured from isotope dilution were similar to estimates from CNCPS (v. 6.55), but a lower proportion of absorbed AA was derived from MCP for the former method. Compared with the isotope and CNCPS estimates, the Fleming model underestimated microbial EAA and total EAA availability. An average of 58% of the absorbed EAA was converted into milk, which varied among individual AA and was interactively affected by starch and RDP in diets. The isotope dilution approach is advantageous because it provides estimates of EAA availability for individual EAA from rumen-undegradable protein and MCP directly with fewer errors of measurement than can be achieved with intestinal disappearance methods.

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