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         <h1>Overview</h1>
-        <p>Our composite parts, consists of three variants of reporter systems and an Antisense Oligonucleotide (ASO) system. Our ASO system (<a href = "https://parts.igem.org/Part:BBa_K5401006">BBa_K5401006</a>) is a strong contender for the best composite part due to its innovative design and practical applications. The utilisation of an ASO helps to regulate the expression of T7RNAP, thereby allowing for the stable expression of the polymerase. The ASO system provides precise control over gene regulation by inhibiting translation, which is essential for fine-tuning gene expression in various experimental contexts.
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-            In addition, our three reporter variants demonstrates the versatile monitoring of gene expression, enabling researchers to choose the most effective system for their specific needs. , 
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-            Taken together, these components enhance the reliability and stability of gene expression, making our composite parts valuable tools in synthetic biology research.</p>
+        <p>Our composite parts, consists of three variants of reporter systems and an antisense oligonucleotide (ASO) system. In particular, our ASO system (<a href = "https://parts.igem.org/Part:BBa_K5401006">BBa_K5401006</a>) is a strong contender for the best composite part due to its innovative design and practical applications. The ASO system provides precise control over gene regulation by inhibiting translation, which is essential for fine-tuning gene expression in various experimental contexts. The utilisation of an ASO helps to regulate the expression of T7RNAP, thereby allowing for the stable expression of the polymerase. In addition, our three reporter variants demonstrate the versatile monitoring of gene expression, enabling researchers to choose the most effective system for their specific needs.</p>
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+        <p>Furthermore, our basic parts entail the two intricate components of our ASO system, the antisense oligonucleotide targeted against the +4 to +27 of the wild-type T7RNAP mRNA sequence, as well as the Hfq scaffold sequence to recruit the Hfq protein for promoting the binding between sRNA and its complementary mRNA target. Three ancestral sequences derived from ancestral reconstruction were also added as part due to their potential as possible distant homologs to the wild-type T7RNAP.</p>
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+        <p>Taken together, our parts continue to contribute to the current inventory of biological systems.</p>
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         <h1>Composite Part</h1>
         <p></p>