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ANNUAL REPORT - Department of Biotechnology

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similarity with the already reported Penaeus<br />

monodon Crustacean Hyperglycemic Hormone 1<br />

precursor gene complete cds. Primers for amplifying<br />

CDS <strong>of</strong> GIH gene were designed from the conserved<br />

region <strong>of</strong> the available GIH gene sequence <strong>of</strong><br />

Lobsters and Metapenaeus sp. Total RNA isolation<br />

from the eyestalk <strong>of</strong> shrimp was standardized and<br />

the method yielded sufficient amount <strong>of</strong> good quality<br />

total RNA for further purification and analysis.<br />

Patents<br />

a. PAT/4.9.2/06052: Biocontrol <strong>of</strong> luminous bacteria<br />

in shrimp hatcheries using bacteriophages<br />

b. PAT/4.9.15/06053: Oligonucleotide probe for<br />

detection and enumeration <strong>of</strong> Vibrio spp. in<br />

aquaculture systems<br />

Technologies transferred<br />

- Technology for Biocontrol <strong>of</strong> luminous bacteria in<br />

shrimp hatcheries has been transferred to<br />

Mangalore Biotech Laboratory<br />

Seribiotechnology<br />

A programme on application <strong>of</strong> biotechnology for<br />

improving the productivity and enhancing the quality<br />

<strong>of</strong> silk alongwith the improvement <strong>of</strong> host-plants<br />

continued during the year. A brainstorming session<br />

on application <strong>of</strong> biotechnology for tasar culture was<br />

organized in collaboration with Central Silk Board<br />

(CSB) during November 17-18, 2006 at Central<br />

Tasar Researh and Training Institute, Ranchi.<br />

Significant achievements during the year are<br />

summarized below:-<br />

Development <strong>of</strong> better races <strong>of</strong> silkworm for<br />

increased productivity<br />

Lysozyme-like proteins (LLPs) identified in Bombyx<br />

mori and Antheraea mylitta exhibited a broadspectrum<br />

anti-bacterial activity jointly at Centre for<br />

DNA Fingerprinting and Diagnostics (CDFD),<br />

Hyderabad and National Institute <strong>of</strong> Immunology<br />

(NII), New Delhi. Phylogenetic analysis clustered<br />

LLPs with some uncharacterized lysozyme-like<br />

DBT Annual Report 2006-07<br />

94<br />

proteins from Anopheles and Drosophila and not with<br />

the classical lysozymes. At the Central Sericultural<br />

Germplasm Resource Centre (CSGRC), Hosur work<br />

has been carried out to identify variable regions<br />

existing in the diapause (NB4D 2)<br />

and non-diapause<br />

(Pure Mysore) silkworm (B. mori) races and to corelate<br />

with diapause gene expression. High<br />

homology percentage between the diapause and the<br />

non-diapause indicates that there is no difference in<br />

the genomic organization <strong>of</strong> the diapause gene in<br />

both silkworm races. Expression pattern <strong>of</strong> the<br />

diapause related genes is being studied.<br />

A network project involving five institutions: CDFD,<br />

Hyderabad; Seribiotech Research Laboratory,<br />

Bangalore; Central Sericultural Research and<br />

Training Institute, Mysore; Andhra Pradesh State<br />

Sericulture Research and Development Institute<br />

(APSSR&DI), Hindupur; and Karnataka State<br />

Sericulture Research and Development Institute,<br />

Bangalore continued with a view to identify<br />

baculovirus resistant strains and DNA markers linked<br />

to baculovirus resistance in silkworm (Bombyx mori).<br />

Screening <strong>of</strong> silkworm germplasm for baculovirus<br />

resistance has resulted in identification <strong>of</strong> three<br />

strains each <strong>of</strong> bivoltine and multivoltine. Out <strong>of</strong><br />

these, most resistant strain has been used as a donor<br />

parent to cross with the most susceptible strain to<br />

raise a mapping population, which is being used to<br />

map the markers that are polymorphic between<br />

parental strains. In a collaborative project at the<br />

University <strong>of</strong> Delhi, Delhi and Central Muga Eri<br />

Research & Training Institute, Jorhat, morphometric<br />

data were collected, compiled for 14 populations <strong>of</strong><br />

muga silkworm (Antheraea assama) and maintained<br />

at Jorhat, Assam. Seventeen microsatellite primers<br />

provided by CDFD, Hyderabad and other repetitive<br />

sequence derived primers were successfully tested<br />

by PCR with A. assama DNA. A distinct polymorphic<br />

band <strong>of</strong> 1.4 kbp size was successfully cloned and<br />

sequenced from A. assama. Work is underway to<br />

screen population with more molecular markers and<br />

statistically analyze data for population genetic<br />

diversity.<br />

Studies have been continued on genetic analysis <strong>of</strong>

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