Summary Hydrogen is a promising alternative to fossil fuel for a source of clean energy. Thermophilic biohydrogen production is beneficial for obtaining high H2 production yield. This review recapitulates the basic metabolic pathways in bacteria for hydrogen production and the enzymes involved in various thermophilic hydrogen producing pathways in microorganisms. It also focuses on the current status of thermophilic biohydrogen production through fermentation of commercially viable substrates, such as agricultural residues. The use of metabolic engineering to attain certain physiological desirable characteristics in H2‐producing microorganisms, culture conditions, and types of bioreactors to be used are reviewed. Major obstacles in industrial production of biohydrogen like low volumetric hydrogen production and its environmental impact are identified. The review has further identified current limitations in the commercial thermophilic hydrogen production and suggested methods like the use of heat exchangers and effluent recirculation to reduce the production cost. Copyright © 2015 John Wiley & Sons, Ltd.

Chronic lead exposure is related to many health diseases in mammals. Exposure to lead forms reactive oxygen species reducing body antioxidant enzymes inflicting injury to numerous macromolecules or cell necrosis. Recent studies have revealed oxidative stress as the vital mechanism for lead toxicity. Lead is found to be toxic to several organ systems such as hematopoietic, skeletal, renal, cardiac, hepatic, and reproductive systems and extremely toxic to the central nervous system (CNS). Curcumin, an active ingredient of the dietary spice, and nanocurcumin, a nanoform of curcumin, are found to decrease toxicity due to lead in various organ systems in mouse models. Higher bioavailability, chelating property, and retention time of nanocurcumin over bulk curcumin may pave the way to expand the utility of nanocurcumin to remove lead toxicity from various organ systems within humans.

DNA methyltransferase 1 (DNMT1) is a relatively large protein family responsible for maintenance of normal methylation, cell growth and survival in mammals. Toxic industrial chemical exposure associated methylation misregulation has been shown to have epigenetic influence. Such misregulation could effectively contribute to cancer development and progression. Methyl isocyanate (MIC) is a noxious industrial chemical used extensively in the production of carbamate pesticides. We here applied an in silico molecular docking approach to study the interaction of MIC with diverse domains of DNMT1, to predict cancer risk in the Bhopal population exposed to MIC during 1984. For the first time, we investigated the interaction of MIC and its hydrolytic product (1,3-dimethylurea) with DNMT1 interacting (such as DMAP1, RFTS, and CXXC) and catalytic (SAM, SAH, and Sinefungin) domains using computer simulations. The results of the present study showed a potential interaction of MIC and 1,3-dimethylurea with these domains. Obviously, strong binding of MIC with DNMT1 interrupting normal methylation will lead to epigenetic alterations in the exposed humans. We suggest therefore that the MICexposed individuals surviving after 1984 disaster have excess risk of cancer, which can be attributed to alterations in their epigenome. Our findings will help in better understanding the underlying epigenetic mechanisms in humans exposed to MIC.

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