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The circuit in the first stage compares the magnitudes and routes the big number to the signb, expb, and f r a c b signals and the smaller number to the s i g n s , exps, and f r a c s signals. The comparison is done between expl&fr a c l and exp2&frac2. It implies that the exponents are compared first, and if they are the same, the significands are compared. The circuit in the second stage performs alignment. It first calculates the difference between the two exponents, which is expb-exps, and then shifts the significand, f r a c s , to the right by this amount. The aligned significand is labeled f raca. The circuit in the third stage performs sign-magnitude addition, similar to that in Section 3.7.2. Note that the operands are extended by 1 bit to accommodate the carry-out bit. The circuit in the fourth stage performs normalization, which adjusts the result to make the final output conform to the normalized format. The normalization circuit is constructed in three segments. The first segment counts the number of leading zeros. It is somewhat like a priority encoder. The second segment shifts the significands to the left by the amount specified by the leading-zero counting circuit. The last segment checks the carry-out and zero conditions and generates the final normalized number.





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of cells to alkaline conditions at higher residence times in the PFR. Exposure of cells to the higher-pH environment did not affect the growth of the culture. The results from the scale-down studies clearly showed that cellular metabolism of this culture was affected by pH uctuations at PFR residence times of 60 s or higher. It was proposed that these changes in metabolism may be linked to both the sensitivity of the acetoin and 2,3-butanediol forming enzymes to pH and to the inducing effects of dissociated acetate on the acetolactate synthase enzyme (Amanullah et al., 2001b). It is well recognized that the optimum location for the addition and subsequent dispersion of any inlet feed, such as acid or base for pH control or glucose in fed-batch fermentations, is in the impeller region due to the prevailing high turbulence. (See 13 for further discussion of local mixing effects.) This would also reduce any overshoot from the set point, since the pH probe is generally in the close vicinity of this region. It is recommended to locate any pH feed near an impeller, perhaps employing several feeding points in order to eliminate or reduce pH uctuations and their effect on microbial metabolism. A recent study of large scale free-suspension animal cell culture has shown such a change to be necessary and effective (Langheinrich and Nienow, 1999). Also, a comparison of the performance of large scale and scale-down experiments with respect to glucose feeding in E. coli fermentations for recombinant protein production also concluded that a two-feed-point glucose addition was superior to a single feed addition in preventing unwanted acetate formation at the large scale (Bylund et al., 1999).

If you need a refresher on the RFC 822 and W3CDTF date/time formats, they were first mentioned in this book back in 7. You may want to flip back there if you want more details.

Listing 5-5 (continued)

The Artboard tool allows you to change existing Artboards and create new Artboards. The Artboard tool is in the lower half of the Tools panel, as shown in Figure 3.5. As soon as you select the Artboard tool, the screen changes, making everything outside the Artboard area darkened and putting a big dashed line around the Artboard. The Control panel also changes, displaying the options shown in Figure 3.6.

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