Detection of the IAA Biosynthetic Pathway from Tryptophan via Indole-3-Acetamide in Bradyrhizobium spp.

The IAA biosynthetic pathway of tryptophan to IAA via IAM wasdetected in Bradyrhizobium spp. (slow-growing Rhizobium) butnot in Rhizobium spp. (fast-growing Rhizobium). A simple methodusing rapid HPLC analysis to measure the conversion from NAMto NAA was developed to detect indole-3-acetamide hydrolaseactivity in cultures of bacteria. Most of the Bradyrhizobiumstrains produce large amounts of NAA converted from NAM underour assay conditions. In addition, GC/MS analysis of purifiedextracts from cultures of B.japonicum wild-type strain J1063,grown in a tryptophan-supplemented liquid medium, demonstratedthe presence of IAM and IAA. The results strongly suggest thatbiosynthesis of IAA in Bradyrhizobium spp. involves the samepathway as that operating in Pseudomonas savastanoi and Agrobacteriumtumefaciens. (Received December 25, 1988; Accepted May 18, 1988)     

Tumorization-Redifferentiation System of Tobacco Genetic Tumor

Genetic tumor was easily and rapidly induced by cutting treatmentof tobacco (Nicotiana glauca ? N. langsdorffu) F₁ seedlingsin a simplified system in vitro. When this tumor was culturedunder weakened light intensity normal shoots developed frequently.After these shoots were maintained under appropriate light conditions(ca. 2–3 W/m²) they regenerated into whole plants withnormal appearance. The regenerated plants were identical tothose developed after germination with respect to their responseto cutting treatment. Using this system we are able to switchthe morphology between the tumorous state and the normal staterapidly and with ease. The significance and the implicationsof the availability of this system for studies of the mechanismof conversion between these two states at the molecular levelare discussed. (Received March 30, 1988; Accepted September 22, 1988)     

Comparison of laboratory-reared eggs, embryos and larvae of five labrid fishes

Eggs, embryos and larvae of five labrid fishes, Thalassoma cupido, Pteragogus flagellifer, Pseudolabrus japonicus, Halichoeres tenuispinnis, and H. poecilopterus, reared in the laboratory are described and compared. The eggs were buoyant and spherical, with a single, spherical oil globule. P. japonicus eggs were unique in lacking melanophores on the oil globule. Eggs of the remaining species closely resembled each other, except in diameter. Incubation periods were short, ranging from ca. 19 h in H. poecilopterus to ca. 31 h in P. japonicus. The newly-hatched embryos also resembled each other, having a short tail and large oval or pear-shaped yolksac, the anterior tip of which extended beyond the snout. The single oil globule was located at the anterior tip of the yolk. As the yolksac diminished with growth, its anterior tip moved posteriorly. The yolk and oil globule were completely absorbed 3 or 4 days after hatching. In all free embryos and larvae except for Pteragogus flagellifer, needle-like projections appeared on both the dorsal and anal finfold margins 12 h to 1 day after hatching. Although morphology of free embryos and larvae of all five species was very similar, differences in pigmentation, location of the anus, and the needle-like projections were apparent. Artificial keys to the newly-hatched embryos and larvae are given.     

Interleukin 2 promotes expression of an interleukin 2 receptor and proliferation of T cells stimulated with non-mitogenic dose of concanavalin A

Interleukin 2 (IL-2) initiated proliferation of the cells of T-enriched population stimulated with non-mitogenic dose of concanavalin A (Con A), whereas it could not induce proliferation of the cells treated with non-mitogenic lectin wheat germ agglutinin (WGA). Use of monoclonal antibody (MAb) directed against interleukin 2 receptor (IL-2R) showed that IL-2 significantly increased expression of IL-2R on the cells of T-enriched population stimulated with Con A, whereas it could not cause any significant enhancement of expression of IL-2R on the cells treated with WGA. We concluded that IL-2 activated T cells in combination with non-mitogenic does of Con A, and induced both expression of IL-2R and proliferation.