A series of trials was conducted to determine the effects of supplemental rumen-protected methionine (RPMet) and lysine (RPLys) on nutrient metabolism and performance. In situ RPMet N disappearance was less than 4% following 48 h of incubation and was not affected (P greater than .05) by diet or resultant ruminal pH differences, indicating that RPMet was well protected from ruminal microbial degradation. Thirty-five Dorset-sired crossbred wether lambs (avg wt 28 kg) fed ground corn-soybean hull diets supplemented with urea were randomly assigned to one of the following treatments: 1) 0% RPMet, 2) .03% RPMet, 3) .06% RPMet, 4) .09% RPMet or 5) .12% RPMet. Dry matter, fiber and N digestibilities and N retention were not affected (P greater than .05) by treatment. Plasma methionine concentration tended to increase linearly (P less than .07) with dietary RPMet level. Six Simmental X Angus steers (avg wt 427 kg) were fed a corn grain-corn silage diet supplemented with urea and five levels of RPMet: 1) 0%, 2) .04%, 3) .08%, 4) .12% and 5) .16%. The plasma methionine concentration increased linearly (P less than .01) with dietary RPMet level. In a steer performance trial, no improvements in feedlot performance resulted due to these RPMet levels (P greater than .05), suggesting that the control diet (0% RPMet) was meeting the methionine requirement of these steers. The effects of RPMet and RPLys on growing and finishing steer feedlot performance also were evaluated. Treatments were 1) urea control, 2) soybean meal positive control, 3) .09% RPMet + .06% RPLys, 4) .12% RPMet + .08% RPLys and 5) .15% RPMet + .10% RPLys. In the growing trial, added RPMet and RPLys did not improve steer feedlot performance. In the finishing trial, only steers fed .09% RPMet + .06% RPLys had higher (P less than .05) gains than those fed the urea control diet. These trials indicate that postruminal methionine and lysine supplies were not limiting feedlot steer performance.
Lactobacillus sake L13, an isolate from vacuum packaged beef is able to utilise cysteine as an energy source for growth in rich medium. This isolate segregates into two strains, one of which retains the ability to grow on cysteine (notated as strong cells) while the other grows only marginally (weak). Both strains possess cysteine desulfhydrase activity, but only one is able to actively transport cysteine (high affinity). Uptake is sensitive to inhibition by valinomycin, CCCP, nigericin and arsenate. Comparison of the two cell types indicates that there are two cysteine transport systems and that the alternative one is passive and of low affinity. Strong cells possess two plasmids (2.7 and 8.3 kb) while the weak strain has lost the plasmids. Curing of the strong cells results in plasmid loss and loss of the high affinity cysteine uptake system.
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