What is the Difference Between EcoRI and HindIII Restriction Enzymes?

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EcoRI and HindIII are both type II restriction enzymes that cleave double-stranded DNA at specific recognition sites. However, they have some differences in their specificity and requirements for cofactors:

  1. Origin: EcoRI is isolated from the bacterial species E.coli, while HindIII is isolated from Haemophilus influenza species.
  2. Recognition Site: EcoRI has a recognition site of 5'-GAATTC-3', and it cleaves at the sequence 5'-AATTC-3'. HindIII, on the other hand, has a recognition site of 5'-AAGCTT-3', and it cleaves at the sequence 5'-AGCTT-3'.
  3. Cofactor: Both enzymes require Mg2+ as a cofactor for their specific activity. However, HindIII has catalytic activity only in the presence of Mg2+ and performs poorly when this ion is substituted for other cofactors such as Mn2+.
  4. Purpose: EcoRI was instrumental in the first recombination DNA experiment and has been widely used in molecular biological research. HindIII is commonly used in the pharmaceutical industry for the production of biopharmaceuticals, such as monoclonal antibodies, recombinant proteins, and DNA vaccines.

In summary, EcoRI and HindIII are type II restriction enzymes with distinct recognition sites and cofactor requirements. They play crucial roles in molecular biological research and biotechnological applications.

Comparative Table: EcoRI vs HindIII Restriction Enzymes

EcoRI and HindIII are both type II restriction enzymes, but they have some differences in their characteristics and functions. Here is a table summarizing their differences:

Feature EcoRI HindIII
Bacterial Species E. coli Haemophilus influenzae
Recognition Sequence 5'GAATTC3' 5'AAGCTT3'
Sticky Ends 5' End Overhangs AATT AAG
Molecular Mass 31 kDa 34.9 kDa
Subunit Structure Homodimer of a 31 kDa subunit containing one globular domain of the α/β architecture Homodimer with a common structural core comprising four β sheets and a single α helix

Both EcoRI and HindIII are Type II restriction enzymes, which means they recognize and cut DNA at specific sites within their recognition sites. They produce sticky ends after cutting DNA, which are single-stranded overhangs that can anneal to other DNA molecules with complementary sticky ends. This property is widely used in modern molecular biological research, such as DNA sequencing, cloning, and genetic engineering.