Martin Gibbs and the peaceful uses of nuclear radiation, (14)C.

This abstract is a prologue to this paper. Prior to his health failing, Martin Gibbs began writing remembrances of his education and beginning a science career, particularly on the peaceful uses of nuclear radiation, at the U.S. Brookhaven National Laboratory (BNL), Camp Upton, NY. Two years before his death Martin provided one of us (Govindjee) a draft text narrating his science beginnings in anticipation of publication in Photosynthesis Research. Govindjee edited his draft and returned it to him. Later, when it became difficult for him to complete it, he phoned Govindjee and expressed the desire that Govindjee publish this story, provided he kept it close to his original. Certain parts of Martin's narrations have appeared without references (Gibbs 1999). The Gibbs family made a similar request since the narrations contained numerous early personal accounts. Clanton Black recently presented an elegant tribute on Martin Gibbs and his entire science career (Black 2008). Clanton was given the draft, which he and Govindjee then agreed to finish. This chronicle is their effort to place Gibbs's narrations about his education and his maturation scientifically, in context with the beginnings of biological chemistry work with carbon-14 at the BNL (see Gibbs 1999). Further, these events are placed in context with those times of newly discovered radioisotopes which became available as part of the intensive nuclear research of World War II (WW II). Carbon-14, discovered during WW II nuclear research in 1940, was extremely useful and quickly led to the rapid discovery of new carbon metabolism pathways and biochemical cycles, e.g., photosynthetic carbon assimilation, within a decade after WW II.

Martin Gibbs (1922-2006): Pioneer of (14)C research, sugar metabolism & photosynthesis; vigilant Editor-in-Chief of Plant Physiology; sage Educator; and humanistic Mentor.

The very personal touch of Professor Martin Gibbs as a worldwide advocate for photosynthesis and plant physiology was lost with his death in July 2006. Widely known for his engaging humorous personality and his humanitarian lifestyle, Martin Gibbs excelled as a strong international science diplomat; like a personal science family patriarch encouraging science and plant scientists around the world. Immediately after World War II he was a pioneer at the Brookhaven National Laboratory in the use of (14)C to elucidate carbon flow in metabolism and particularly carbon pathways in photosynthesis. His leadership on carbon metabolism and photosynthesis extended for four decades of working in collaboration with a host of students and colleagues. In 1962, he was selected as the Editor-in-Chief of Plant Physiology. That appointment initiated 3 decades of strong directional influences by Gibbs on plant research and photosynthesis. Plant Physiology became and remains a premier source of new knowledge about the vital and primary roles of plants in earth's environmental history and the energetics of our green-blue planet. His leadership and charismatic humanitarian character became the quintessence of excellence worldwide. Martin Gibbs was in every sense the personification of a model mentor not only for scientists but also shown in devotion to family. Here we pay tribute and honor to an exemplary humanistic mentor, Martin Gibbs.

Crassulacean acid metabolism photosynthesis: ;working the night shift'.

Crassulacean acid metabolism (CAM) can be traced from Roman times through persons who noted a morning acid taste of some common house plants. From India in 1815, Benjamin-Heyne described a 'daily acid taste cycle' with some succulent garden plants. Recent work has shown that the nocturnally formed acid is decarboxylated during the day to become the CO(2) for photosynthesis. Thus, CAM photosynthesis extends over a 24-hour day using several daily interlocking cycles. To understand CAM photosynthesis, several landmark discoveries were made at the following times: daily reciprocal acid and carbohydrate cycles were found during 1870 to 1887; their precise identification, as malic acid and starch, and accurate quantification occurred from 1940 to 1954; diffusive gas resistance methods were introduced in the early 1960s that led to understanding the powerful stomatal control of daily gas exchanges; C(4) photosynthesis in two different types of cells was discovered from 1965 to approximately 1974 and the resultant information was used to elucidate the day and night portions of CAM photosynthesis in one cell; and exceptionally high internal green tissue CO(2) levels, 0.2 to 2.5%, upon the daytime decarboxylation of malic acid, were discovered in 1979. These discoveries then were combined with related information from C(3) and C(4) photosynthesis, carbon biochemistry, cellular anatomy, and ecological physiology. Therefore by approximately 1980, CAM photosynthesis finally was rigorously outlined. In a nutshell, 24-hour CAM occurs by phosphoenol pyruvate (PEP) carboxylase fixing CO(2)(HCO(3) (-)) over the night to form malic acid that is stored in plant cell vacuoles. While stomata are tightly closed the following day, malic acid is decarboxylated releasing CO(2) for C(3) photosynthesis via ribulose bisphosphate carboxylase oxygenase (Rubisco). The CO(2) acceptor, PEP, is formed via glycolysis at night from starch or other stored carbohydrates and after decarboxylation the three carbons are restored each day. In mid to late afternoon the stomata can open and mostly C(3) photosynthesis occurs until darkness. CAM photo-synthesis can be both inducible and constitutive and is known in 33 families with an estimated 15 to 20 000 species. CAM plants express the most plastic and tenacious photosynthesis known in that they can switch photosynthesis pathways and they can live and conduct photosynthesis for years even in the virtual absence of external H(2)O and CO(2), i.e., CAM tenaciously protects its photosynthesis from both H(2)O and CO(2) stresses.

Temporal and spatial aspects of root and stem sucrose metabolism in loblolly pine trees.

We studied root and stem sucrose metabolism in trees excavated from a 9-year-old artificially regenerated loblolly pine (Pinus taeda L.) plantation. Sucrose synthase (SS) activities in stem and taproot vascular cambial tissues followed similar seasonal patterns until they peaked during September. After September, stem SS activity disappeared quickly, whereas taproots exhibited SS activity even in January. Pyrophosphate-dependent phosphofructokinase (PPi-PFK) activity tracked SS activity. The activities of ATP-dependent PFK and several other glycolytic enzymes (e.g., phosphoglucomutase and phosphoglucoisomerase) remained relatively constant in cambial tissues of stem, taproot, and all first-order lateral roots (FOLRs) throughout the year. However, during the growing season, individual FOLRs exhibited variable sucrose metabolic activities that were independent of root diameter or position on the taproot. The FOLRs with low or no SS activity also had low PPi-PFK activity. We propose that when intense competition for sucrose occurs among different organs of a tree, the variable activities of the sucrose metabolic enzymes in FOLRs ensure that enough sucrose is allocated to the stem and taproot for growth. For a tree's long-term survival and growth, second or higher-order roots can be sacrificed, whereas FOLRs, stem and taproot are essential.