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Fig. 1 | Microbial Cell Factories

Fig. 1

From: Characterization and high-efficiency secreted expression in Bacillus subtilis of a thermo-alkaline β-mannanase from an alkaliphilic Bacillus clausii strain S10

Fig. 1

Multiple amino acid sequence alignment. The enzymes used were BcManA, BacEndoG from Bacillus clausii (GenBank No.WP_041823500.1), BacMan-K16 from B. clausii KSM-K16 (GenBank No. BAD62862.1), BaaMan5A from B. agaradhaerens (UniProtKB/Swiss-Port G1K3N4.1), BspMan-165 from Bacillus sp. N16-5 (GenBank No. AAT06599.1), BspMan-602 from Bacillus sp. JAMB-602 (BAD99527.1), BacMan-1554 from B. circulans CGMCC1554 (GenBank No. AAX87003.1), and BacMan-K1 from B. circulans K-1 (GenBank No. BAA25878.1). Strictly conserved residues are shaded black and conservatively substituted residues are boxed. Circles indicate the conserved catalytic sites. The figure was produced using ESPript 3.0 (http://espript.ibcp.fr/ESPript/ESPript/index.php). The arrow shows the cleavage site of the signal peptide of BcManA

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Microbial Cell Factories

ISSN: 1475-2859

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