Department of Molecular Biosciences and Bioengineering - College of Tropical Agriculture and Human Resources - University of Hawai'i at Manoa

Dulal Borthakur

Professor Dulal Borthakur

Current Research

Development of mimosine-free L. leucocephala: We have been working on molecular biology and biochemistry of mimosine degradative pathway in root nodule bacteria.  Recently, we have constructed a hybrid gene by combining the pydA and pydB of Rhizobium sp. strain TAL1145.  pydA codes for a dioxygenase, while pydB encodes a hydrolase, and both these enzymes are essential for degradation of 3-hydroxy-4-pyridone (HP) which is an intermediate of mimosine degradation.  HP is also a precursor for mimosine biosynthesis in leucaena.  The pydA-pydB hybrid gene encodes a PydA-PydB fusion protein that has both the dioxygenase activity of PydA and the hydrolase activity of PydB.  We are now transferring the hybrid gene into L. leucocephala.  It is expected that the transgenic leucaena expressing the pydA-pydB hybrid gene will have reduced amount of mimosine. 

Microsatellite markers for Acacia koa (koa):  Koa is an important tree legume endemic to Hawaii.  The koa forests are distributed in all major Hawaiian Islands.  We are developing microsatellite markers for determining genetic diversity among the koa tree populations in different islands. 

Development of recombinant vaccines against Mycobacerium tuberculosis: The aim of this project is to identify potential subunit protein vaccine candidates for immunization against Mycobacterium tuberculosis (Mtb).  The focus is to produce an immune response that is MHC genotype specific and elicits elevated levels of interferon gamma (IFN-g), characteristic of a protective response.  Bioinformatic, molecular and proteomic tools were employed to identify putative vaccine candidate peptides.  In addition, hybrid peptides containing a number of immunogenic epitopes are being tested in mice to determine whether they might be more protective than the individual components.  An in silico genomic subtraction of the tuberculosis vaccine strain of Mycobacterium bovis, BCG-Denmark from Mtb H37Rv, yielded 61 genes that are unique to the primary disease-causing agent, Mtb.  Further, an in silico analysis platform is being developed to evaluate the potential genes for immune reactivity by mimicking proteasomal digestion, transport-associated antigen selection and H-2 antigen presentation. In addition to Mtb infections, this approach can be used to find host genotype-specific vaccine candidates for other related intracellular pathogens

Recent publications

Other academic activities

Chairman, Graduate Program in Molecular Biosciences and Bioengineering, University of Hawaii (1996 - present).


Awards

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