This anomaly is indicative of the larger challenge of culturing various microbial species, referred to as microbial “unculturability.” This cannot be explained by the use of agar alone or by the substitution of an alternative gelling agent, but rather by the difficulties in consistently recreating on an agar plate the multi-variable environment in which microbes grow naturally. Given such challenges, the risk of shortages, and the vulnerabilities of the agar supply chain, why is it so difficult to find suitable alternatives?
I'm building an 80386-compatible core in SystemVerilog and blogging the process. In the previous post, we looked at how the 386 reuses one barrel shifter for all shift and rotate instructions. This time we move from real mode to protected and talk about protection.
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