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@@ -255,8 +255,8 @@ <h2>Construction of <i>hmaS</i> Mutant Library</h2>
 									positive clones
 									was 100%.</p>
 								<div class="figure-container" style="width: 80%;margin: 0 auto;">
-									<img src="../../images/图片1.png" alt="">
-									<p>gY9s-HmaS<sup>mut</sup>-Bio177 mutant library plates</p>
+									<img src="../../images/a4.jpg" alt="">
+
 								</div>
 
 								<p><b>Figure 1.</b> A mutant library with 10⁵ clones was constructed by using a
@@ -302,7 +302,7 @@ <h2>Construction and Test of a Dual-Module Screening Platform</h2>
 									concentrations, the selection pressure
 									accelerated, which enhanced the performance of viable individuals, improved HMA
 									production, and reduced fluorescence
-									strength. Based on colony fluorescence and HMA production, we screened clones under
+									intensity. Based on colony fluorescence and HMA production, we screened clones under
 									the conditions of 0.6 g/L HPP and
 									0.3 mg/L 5-FC (Fig. 3). And we found a mutant clone HmaS<sup>V152G</sup> that HMA
 									production of
@@ -321,8 +321,8 @@ <h2>Construction and Test of a Dual-Module Screening Platform</h2>
 									<img src="../../images/t8.jpg" alt="">
 								</div>
 								<p><b>Figure 4.</b> Graph of HMA production by the bacteria harboring
-									HmaS<sup>WT</sup>and
-									HmaS<sup>V152G</sup>clones. With 9 mM HPP as the substrate for
+									HmaS<sup>WT</sup> and
+									HmaS<sup>V152G</sup> clones. With 9 mM HPP as the substrate for
 									whole-cell catalysis, HMA accumulation by the gY9s-HmaS<sup>V152G</sup>-Bio177 and
 									gY9s-HmaS<sup>WT</sup>-Bio177 strains was monitored for 3
 									h.</p>
@@ -374,7 +374,7 @@ <h2>Engineering an <i>E. coli</i> Chassis with High-HPP Production</h2>
 								<p>we constructed the pSB1c-aroG<sup>fbr</sup>-tktA-ppsA (pATP) plasmid to
 									overexpress the
 									phosphoenol-pyruvate synthase (<i>ppsA</i>) gene,
-									the transketolase (<i>tktA</i>) gene and aro<i>G<sup>fbr</sup></i>gene.
+									the transketolase (<i>tktA</i>) gene and <i>aroG<sup>fbr</sup></i> gene.
 									Through the modifications of
 									genetic
 									overexpression, we obtained a host
@@ -400,7 +400,7 @@ <h2>Engineering an <i>E. coli</i> Chassis with High-HPP Production</h2>
 								<div class="figure-container" style="width: 60%;margin: 0 auto;">
 									<img src="../../images/26.jpg" alt="">
 								</div>
-								<p><b>Figure 7.</b> Bar graph of the Inhibitory efficiency by the random
+								<p><b>Figure 7.</b> Bar graph of the inhibitory efficiency by the random
 									double-mismatched eGFP-sgRNAs. Fi means fully interference,
 									transformed into the strain that containing the non-mutated R6K-dCas9-eGFP
 									plasmid, which had CA in the 7-8bp spacer of