Celebrating a century of scientific innovation that transformed our understanding of cellular life and scientific communication
Imagine a scientist who began his career treating patients with penicillin during its first clinical trials, pioneered a fundamental field of biochemistry, and then revolutionized how scientific knowledge is shared across the globe—all while working at the same institution for 77 years.
This was Herbert Tabor, a man whose life spanned 101 years but whose impact will extend for centuries. Through his groundbreaking research on polyamines and his transformative leadership of the Journal of Biological Chemistry (JBC), Tabor became the invisible architect of modern biochemistry, designing the very frameworks through which we understand cellular life and disseminate scientific discovery 1 .
At a time when scientific publishing moved at the pace of printed pages and postal services, Tabor envisioned a world where research could be accessed instantly by anyone, anywhere. When many biochemists focused on flashy, trending topics, he dedicated seven decades to understanding the mysterious polyamines—unassuming molecules that would later be recognized as crucial to life itself.
1918-2020
These organic compounds, with names like putrescine, spermidine, and spermine, are found in virtually every living cell, yet for decades their functions remained mysterious 1 .
Through painstaking research conducted alongside his wife and scientific partner, Celia White Tabor, Herb revealed that these seemingly simple molecules are actually master regulators of cellular function 4 .
The Tabors discovered that polyamines interact intimately with DNA, RNA, and proteins, influencing everything from cell growth to how organisms respond to stress 1 .
They demonstrated that without polyamines, most cells simply cannot grow properly 5 . These compounds protect against oxidative damage, extreme temperatures, and other environmental threats while maintaining the proper function of mitochondria 1 .
The Tabors mapped the intricate biochemical pathways through which cells produce polyamines 2 .
Polyamines regulate the expression of genes involved in their own synthesis—a sophisticated feedback mechanism 2 .
Their research demonstrated how polyamines help cells survive under stressful conditions 1 .
In 1958, Herbert and Celia Tabor published a groundbreaking paper that would become a cornerstone of polyamine research: "The biosynthesis of spermidine and spermine from putrescine and methionine" .
Their experimental approach involved several meticulous steps:
Used radioactive carbon-14 and hydrogen-3 (tritium) to label precursor molecules .
Labeled precursors were incubated with enzyme extracts from bacteria and rat liver tissues .
Employed paper chromatography and ion-exchange chromatography to isolate compounds .
Radioactive labels enabled detection and quantification of biochemical conversions .
The Tabors' experiment yielded clear and compelling results that illuminated the previously mysterious biosynthesis pathway of spermidine.
| Precursor Used | Radioactive Label | Resulting Product | Significance |
|---|---|---|---|
| Putrescine | Carbon-14 | Spermidine | Direct incorporation of putrescine |
| Methionine | Hydrogen-3 | Spermidine | Methionine as methyl group donor |
| Methionine | Radioactive sulfur | S-adenosylmethionine | Identified activated form of methionine |
The data revealed a two-step process: first, putrescine is produced from ornithine; then, a portion of the methionine molecule is transferred to putrescine to form spermidine .
The Tabors' groundbreaking work was made possible by specific research tools and methodologies that defined the field of polyamine biochemistry.
| Research Tool | Function in Polyamine Research | Example from Tabor's Work |
|---|---|---|
| Radioactive labeling (C-14, H-3) | Tracing metabolic pathways and conversions | Tracking putrescine-to-spermidine transformation |
| Chromatography techniques | Separating and identifying polyamines | Isolating spermidine from reaction mixtures |
| Enzyme preparations | Studying biochemical reactions in controlled systems | Using bacterial and liver extracts to study biosynthesis |
| S-adenosylmethionine | Methyl group donor in biochemical reactions | Identified as crucial for spermidine synthesis |
| Ornithine decarboxylase | Rate-limiting enzyme in polyamine pathway | Key regulatory enzyme studied extensively 2 |
While Herbert Tabor's scientific research alone would have secured his legacy, his impact on the world of science extended far beyond the laboratory. As Editor-in-Chief of the Journal of Biological Chemistry from 1971 to 2010, Tabor engineered one of the most significant transformations in the history of scientific communication 3 .
By the early 1990s, the JBC had become a behemoth—the second-most voluminous journal of its time, publishing over 31,000 pages annually across 52 weekly issues 3 . The physical bulk of the journal had become so substantial that Stanford University actually considered it an "earthquake hazard" 3 .
"The journal was approaching the U.S. Postal Service's weight limit for second-class mail, threatening its very distribution. More importantly, the traditional print model meant that groundbreaking research was taking months—sometimes up to a year for international destinations—to reach scientists after acceptance." 3
Tabor recognized that this system was untenable and actively sought solutions. Early experiments with CD-ROMs proved unsatisfactory, as scientists didn't want to wait six months for compiled issues 3 . But in 1995, under Tabor's leadership, the JBC took a revolutionary leap—it became the first scientific journal in the world to publish online 3 .
Tabor's push for digital publication was not without its critics. Some within the American Society for Biochemistry and Molecular Biology worried that the venture might fail and financially cripple both the journal and the society 4 .
His leadership style during this transition was described as uniquely effective—"calm, insightful, and humble," yet firm when necessary. 4
When the Publications Committee once suggested changing the journal's name to something "flashier," Tabor was visibly distressed, recognizing the value of the JBC brand and tradition 4 . The society promptly revised its bylaws to prevent such changes, demonstrating the immense trust and respect colleagues placed in Tabor's judgment.
The impact of this digital transformation cannot be overstated. Almost overnight, JBC Online eliminated the "literature lag" that had slowed scientific progress for centuries 3 . Researchers no longer had to spend hours in library attics hunting for papers or wait months to read about developments in their field 3 .
Herbert Tabor's remarkable career was recognized with numerous honors, including election to the National Academy of Sciences in 1977, the William C. Rose Award (shared with Celia) in 1995, and the Hillebrand Prize from the American Chemical Society in 1986 1 5 .
But perhaps more meaningful to him were the honors established in his name, including the Herbert Tabor Young Investigator Awards and the Herbert Tabor Research Award, which continue to support and recognize excellence in biochemistry 1 .
Herb taught me how to do science, and his devotion to science set a standard for me to aspire to. His gentle sincerity combined with forthright critical thinking made him a leader throughout his career.
Even in his final years, Tabor remained actively engaged in science, working remotely on research papers with NIH colleagues until the very end 1 . His 101-year lifespan connected the earliest days of modern biochemistry with the cutting edge of contemporary research, making him both a pioneer and a bridge between scientific generations.
Herbert Tabor's century of life and 77 years at NIH represent more than just longevity—they embody a consistent commitment to excellence, innovation, and community in science.
Through his groundbreaking work on polyamines, he revealed fundamental truths about how life operates at the molecular level. Through his visionary leadership of the Journal of Biological Chemistry, he transformed how knowledge is shared and how scientific communities form across geographic boundaries.
The true measure of Tabor's legacy lies not in the awards he received or the positions he held, but in the frameworks he built—both conceptual and practical—that continue to guide biochemistry today.
As we continue to build upon the foundations Tabor laid—both in understanding polyamines and in communicating scientific findings—we honor the legacy of this quiet architect of modern biochemistry.