New data on the Rectogordius (foraminifera) abundance zone (Latest Carboniferous: Gzhelian) of the Zaladou Formation (east-central Iran,Tabas block,Shishtu section)

The Rectogordius (Foraminifera) abundance zone is described in the east of the Shishtu village in the Ozbak Kuh Mountain. The samples were collected in the Zaladou Formation., which is 60 m thick and composed of shales, sandstones, sandy limestones, microconglomerate, bioclastic limestones, coral limestone and fusulinid limestones. The Rectogordius abundance zone was found in sandy bioclastic limestone. It displays two species and three subspecies of this foraminifer, including Rectogordius iranicus, R. iranicus gadukensis, R. minimus and R. minimus shishtuensis n. subsp., R. iranicus ozbakensis n. subsp. The age of this abundance zone is considered to be Gzhelian, due to the distribution of Rectogordius in Central Iran (Ozbak Kuh; Zaladou Formation), central and eastern Alborz (Emarat Fm.), Sanandaj-Sirjan zone (Vazhnan Formation), as well as in the Donets, Arctic Canada, Afghanistan, and the Carnic Alps. The genus Rectogordius is possibly restricted to the northern Paleotethys margin, northern Cimmerian margin, shelf of the Uralian Ocean as far as the northernmost part of North America. Two new subspecies Rectogordius minimus shishtuensis n. subsp. and Rectogordius iranicus ozbakensis n. subsp. are described.     

Synthesis and antibacterial activity of novel C12 ethyl ketolides

A novel series of C(12) ethyl erythromycin derivatives have been discovered which exhibit in vitro and in vivo potency against key respiratory pathogens, including those resistant to erythromycin. The C(12) modification involves replacing the natural C(12) methyl group in the erythromycin core with an ethyl group via chemical synthesis. From the C(12) ethyl macrolide core, a series of C(12) ethyl ketolides were prepared and tested for antibacterial activity against a panel of relevant clinical isolates. Several compounds were found to be potent against macrolide-sensitive and -resistant bacteria, whether resistance was due to ribosome methylation (erm) or efflux (mef). In particular, the C(12) ethyl ketolides 4k,4s,4q,4m, and 4t showed a similar antimicrobial spectrum and comparable activity to the commercial ketolide telithromycin. The in vivo efficacy of several C(12) ethyl ketolides was demonstrated in a mouse infection model with Streptococcus pneumoniae as pathogen.     

Adaptation of the parasitic plant lifecycle: germination is controlled by essential host signaling molecules

Parasitic plants are plants that connect with a haustorium to the vasculature of another, host, plant from which they absorb water, assimilates, and nutrients. Because of this parasitic lifestyle, parasitic plants need to coordinate their lifecycle with that of their host. Parasitic plants have evolved a number of host detection/host response mechanisms of which the germination in response to chemical host signals in one of the major families of parasitic plants, the Orobanchaceae, is a striking example. In this update review, we discuss these germination stimulants. We review the different compound classes that function as germination stimulants, how they are produced, and in which host plants. We discuss why they are reliable signals, how parasitic plants have evolved mechanisms that detect and respond to them, and whether they play a role in host specificity. The advances in the knowledge underlying this signaling relationship between host and parasitic plant have greatly improved our understanding of the evolution of plant parasitism and are facilitating the development of more effective control measures in cases where these parasitic plants have developed into weeds.

Root parasitic plants grow on the roots of other plants and germinate only in the presence of that host, on which they completely depend, through the perception of host presence signaling molecules called germination stimulants.

Outstanding questions

• Have we overlooked the role of germination stimulants in facultative parasites?
• What is the biological relevance of the observation that many plant species produce and secrete a range of different strigolactones?
• Have parasitic plants evolved mechanisms to compensate for low phosphorus availability, a condition that stimulates their germination?
• What is the contribution of the HTL strigolactone receptors to host specificity in parasitic plants or does downstream signaling play a role?
• What other, nonstrigolactone, germination stimulants can parasitic plants respond to and does this require adaptation in the HTL receptors?
• What is the role of germination and underlying mechanism in the rapid adaptation of (orobanchaceous) parasitic plants to a new host?

     

Eicosanoids from the Rhodophyta: new metabolism in the algae

Red marine algae are shown in this work to be a rich source of eicosanoid-type natural products. This is the first isolation of several of these mammalian arachidonic acid metabolites from any marine or terrestrial plant source (12-HETE, 12-HEPE, 6(E)-LTB4, hepoxilin B3). A few of these represent truly novel substances never previously isolated from nature [12(R), 13(S)-diHETE]. Inherent in these seaweed natural product structures is evidence for a highly evolved lipoxygenase-type metabolism that matches or exceeds the complexity of comparable metabolic routes in mammalian systems. As these compounds are produced by algae in relatively large quantities (0.1–5.0% of crude lipid extracts), these plants could be important commercial resources for these expensive and rare biochemicals. Further, we suggest that this metabolism is important to physiological processes in red algae that are completely unknown at present. For example, it is possible that they act in an exocrine sense to coordinate reproductive events, a hypothesis under current investigation through culture studies.This paper was presented at the mini-symposium Bioactive Compounds from Algae, Y. Shimizu, Convener.