Paralytic shellfish poisoning (PSP) toxin binders for optical biosensor technology: problems and possibilities for the future: a review

This review examines the developments in optical biosensor technology, which uses the phenomenon of surface plasmon resonance, for the detection of paralytic shellfish poisoning (PSP) toxins. Optical biosensor technology measures the competitive biomolecular interaction of a specific biological recognition element or binder with a target toxin immobilised onto a sensor chip surface against toxin in a sample. Different binders such as receptors and antibodies previously employed in functional and immunological assays have been assessed. Highlighted are the difficulties in detecting this range of low molecular weight toxins, with analogues differing at four chemical substitution sites, using a single binder. The complications that arise with the toxicity factors of each toxin relative to the parent compound, saxitoxin, for the measurement of total toxicity relative to the mouse bioassay are also considered. For antibodies, the cross-reactivity profile does not always correlate to toxic potency, but rather to the toxin structure to which it was produced. Restrictions and availability of the toxins makes alternative chemical strategies for the synthesis of protein conjugate derivatives for antibody production a difficult task. However, when two antibodies with different cross-reactivity profiles are employed, with a toxin chip surface generic to both antibodies, it was demonstrated that the cross-reactivity profile of each could be combined into a single-assay format. Difficulties with receptors for optical biosensor analysis of low molecular weight compounds are discussed, as are the potential of alternative non-antibody-based binders for future assay development in this area

Digestible Lysine Requirements the Performance, Carcass Traits and Breast Meat Quality of Slow-Growing Broilers

ABSTRACT Three experiments were conducted to estimate the digestible lysine requirements of slow-growing broilers on their performance, carcass traits, and breast meat quality. Different broilers were evaluated in each experiment. In Experiment 1, broilers were evaluated from 29-49 days of age (grower phase I), in Experiment 2, from 50 to 69 days old (grower phase II), and in Experiment 3, from 70-84 days old (finisher phase). A completely randomized design with five treatments of four replicates each was applied in all experiments. The following dietary digestible lysine values were investigated: 0.871, 1.011, 1.151, 1.291 and 1.431% in Experiment 1; 0.803, 0.943, 1.083, 1.223 and 1.363% in Experiment 2; and 0.766, 0.906, 1.046, 1.186 and 1.326% in Experiment 3. In all three experiments, digestible lysine values quadratically affected feed intake, weight gain, and feed conversion ratio. Lysine intake linearly increased with increasing digestive lysine values, whereas lysine utilization efficiency linearly decreased. Lysine requirements for maximum feed intake (1.298, 1.109, 1.150%), weight gain (1.183, 1.199, 1.162%), and feed conversion ratio (1.203, 1.162, 1.126%) were estimated in Experiments 1, 2 and 3. Digestible lysine requirement for carcass yield were estimated as 1.162, 1.068 and 1.107% in experiments 1, 2 and 3, respectively. Lysine influenced the physical-chemical parameters broiler breast meat. Digestible lysine levels of 1.203, 1.162 and 1.126% are recommended in the diets of Redbro Plume broilers during the phases 29-49, 50-69 and 70-84 days of age to optimize feed conversion ratio