The accumulation of anthropogenic heavy metals in soil is a major form of pollution. Such potentially toxic elements are nonbiodegradable and persist for many years as threats to human and environmental health. Traditional forms of remediation are costly and potentially damaging to the land. An alternative strategy is phytoremediation, where plants are used to capture metals from the environment. Industrial hemp (Cannabis sativa) is a promising candidate for phytoremediation. Hemp has deep roots and is tolerant to the accumulation of different metals. In addition, the crop biomass has many potential commercial uses after harvesting is completed. Furthermore, the recent availability of an annotated genome sequence provides a powerful tool for the bioengineering of C. sativa for better phytoremediation.

Phosphorus is one of the three macronutrients that are essential for plant growth and development. Inorganic phosphorus (P), which can make up to 70% of the total P content in soils, can exist in calcium-, aluminum-, or iron-complexed forms that are unavailable for plant use. As a result, mineral phosphorus, P2O5, is often used as a fertilizer to supplement the nutrient for crop growth. To reduce the addition of mineral phosphorus to agricultural soils, research in naturally occurring phosphate-solubilizing microorganisms has been conducted for decades. This study found bacteria that solubilized phosphate at very high rates. The most efficient of the bacteria presented in this paper, Pantoea sp. Pot1, can solubilize tricalcium phosphate (Ca3(PO4)2) at a rate of 956 mgL-1. This bacteria produces a variety of organic acids, including acetic, gluconic, formic, and propionic acids. Greenhouse experiments demonstrated that tomato plants with soil systems inoculated with Pantoea sp. Pot1 incorporated more P and produced much higher biomass weights than those plants without any added bacteria.

Many studies have been conducted to produce microbial polyhydroxyalkanoates (PHA), a biopolymer, from Pseudomonas sp. fed with various alkanoic acids. Because this previous data was collected using methodologies that varied in critical aspects, such as culture media and size range of alkanoic acids, it has been difficult to compare the results for a thorough understanding of the relationship between feedstock and PHA production. Therefore, this study utilized consistent culture media with a wide range of alkanoic acids (C7-C14) to produce medium chain length PHAs. Three strains of Pseudomonas putida (NRRL B-14875, KT2440, and GN112) were used, and growth, cell dry weight, PHA titer, monomer distribution, and molecular weights were all examined. It was determined that although all the strains produced similar PHA titers using C7-C9 alkanoic acids, significant differences were observed with the use of longer chain feedstocks. Specifically, KT2440 and its derivative GN112 produced higher PHA titers compared to B-14875 when fed longer chain alkanoates. We also compared several analytical techniques for determining amounts of PHA and found they produced different results. In addition, the use of an internal standard had a higher risk of calculating inaccurate concentrations compared to an external standard. These observations highlight the importance of considering this aspect of analysis when evaluating different studies.