Identification of N-(2-propenal) serine as a urinary metabolite of malondialdehyde

N-2-(Propenal) serine (S-MDA) was synthesized by reacting serine with malondialdehyde (MDA) and was shown to be a 1:1 adduct of the starting materials. The synthetic compound was found to be identical to a metabolite of MDA excreted in rat and human urine. The identity of the metabolite was confirmed by isolation and hydrolysis to yield equimolar quantities of serine and MDA. The presence of S-MDA in urine constitutes direct evidence for oxidative decomposition of phospholipids by lipid peroxidation in vivo.     

Melanin concentrating hormone. III. Melanin concentrating hormone (MCH): the message sequence

Melanin concentrating hormone (MCH) is a heptadecapeptide synthesized by the hypothalamus and secreted by the neurohypophysis of the teleost pituitary gland. MCH stimulates melanosome aggregation within teleost melanocytes but also exhibits MSH-like (melanosome dispersing) activity on tetrapod (frog and lizard) melanocytes. We have synthesized a number of MCH analogues to determine the essential features of the primary structure necessary to stimulate either melanosome aggregation or dispersion in fish or tetrapod melanocytes, respectively. An analysis of the potencies and actions of these analogues on vertebrate melanocytes is provided and demonstrates that the two activities have different structural requirements.     

Inflorescence commitment and subsequent development differ in their responses to temperature and photoperiod in Osteospermum jucundum

Although Osteospermum is a species which is known to require a period of chilling to induce flowering, the precise form of the relationships between temperature and photoperiod on the phases of flowering has not been quantified. This study aimed to investigate the effects of temperature and photoperiod on time to inflorescence commitment and on the rate of subsequent floral development in Osteospermum jucundum cv. Zulu. To assess how temperature and photoperiod affected the number of days needed for inflorescence commitment, plants were transferred from a range of photothermal environments to a non‐inductive environment. The effect of temperature and photoperiod on subsequent inflorescence development was examined by transferring plants with initiated inflorescences to a range of photothermal environments. Inflorescence commitment occurred first in plants grown at a low average diurnal temperature (10.6°C), but no evidence was found to suggest that photoperiod affected the duration of this phase. Once initiated, high temperatures and long days hastened inflorescence development. The rate of progress to flowering from initiation increased linearly with photoperiod and temperature (up to an optimum of 23.5°C).     

Complete topology inversion can be part of normal membrane protein biogenesis

The topology of helical membrane proteins is generally defined during insertion of the transmembrane helices, yet it is now clear that it is possible for topology to change under unusual circumstances. It remains unclear, however, if topology reorientation is part of normal biogenesis. For dual topology dimer proteins such as the multidrug transporter EmrE, there may be evolutionary pressure to allow topology flipping so that the populations of both orientations can be equalized. We previously demonstrated that when EmrE is forced to insert in a distorted topology, topology flipping of the first transmembrane helix can occur during translation. Here, we show that topological malleability also extends to the C‐terminal helix and that even complete topology inversion of the entire EmrE protein can occur after the full protein is translated and inserted. Thus, topology rearrangements are possible during normal biogenesis. Wholesale topology flipping is remarkable given the physical constraints of the membrane and expands the range of possible membrane protein folding pathways, both productive and detrimental.