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30 April 2020 to 19 May 2020 26 June 2020 R Range V60. . Contact Us . We look forward to serving you soon! , [Fig. 2c](#F2){ref-type=”fig”}) points to the low activity level of malate dehydrogenase. The analysis of the granules reveals that the majority of them contained about 6,000 protein molecules; this clearly shows that they are comprised of six granule proteins of about 15 kDa each (magenta, [Fig. 2b](#F2){ref-type=”fig”}) in a 3:3:1 ratio, plus a small amount of fibril proteins (green, [Fig. 2b](#F2){ref-type=”fig”}). A comparison of granules from a mutant strain carrying three isoforms of the SAGA complex and *gerK-L* operon (Δ*sasA* + *sasAgerKL*-loop; [Fig. 2a](#F2){ref-type=”fig”}) reveals that the protein content of the granules is similar to that of wild-type granules. This experiment also shows that three of the six granule proteins are fibril components; indeed, their presence is essential for formation of the mature contact site, as demonstrated by the absence of mature foci in the Δ*sasA* + *sasAgerKL*-loop mutant ([Fig. 2c](#F2){ref-type=”fig”}). This also shows that the stress induced by the *gerK-L* operon is so mild that it does not affect granule assembly, because a Δ*sasA* mutant is as deficient in fibril formation as a Δ*sasA* + *sasAgerKL*-loop mutant. The data for both the wild-type and the Δ*sasA* + *sasAgerKL*-loop strains (with and without a heat shock) are in agreement with results of structural and localization studies showing that SASA (SASA5 in the *B. subtilis* 168 genome, which is presumably SASA4 in the *S. aureus* subsp. *anaerobicus* NCTC8325 genome) and GESAGERKL are part of an fibril scaffold in the mature CSA a2fa7ad3d0


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